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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 792 | 364 | 87 | 69 | 158 | 8 | 40 | 118 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0002 | 0/0 | 792 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0003 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0004 | 0/0 | 792 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2379 | 170 | 52 | 30 | 63 | 2 | 22 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0002 | 0/0 | 2379 | 105 | 2 | 23 | 63 | 4 | 13 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0003 | 1/0 | 2379 | 77 | 22 | 16 | 31 | 2 | 5 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0004 | 0/0 | 2379 | 5 | 5 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0005 | 0/0 | 2379 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0006 | 0/0 | 2379 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0007 | 0/0 | 2379 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0008 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0009 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
c0010 | 0/0 | 2379 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 763 | 272 | 54 | 52 | 124 | 6 | 35 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
t0002 | 1/0 | 764 | 80 | 24 | 15 | 33 | 2 | 5 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
t0003 | 0/0 | 762 | 13 | 12 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
t0004 | 0/0 | 764 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
t0005 | 0/0 | 763 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
t0006 | 0/0 | 763 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 1 | 3 | 7 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0003 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2379 | 170 | 52 | 30 | 63 | 2 | 22 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0002 | 0/0 | 2379 | 105 | 2 | 23 | 63 | 4 | 13 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0003 | 1/0 | 2379 | 77 | 22 | 16 | 31 | 2 | 5 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0004 | 0/0 | 2379 | 5 | 5 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0005 | 0/0 | 2379 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0006 | 0/0 | 2379 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0009 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0002c0007 | 0/0 | 2379 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0003c0010 | 0/0 | 2379 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0004c0008 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | 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 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0001t0002 | 0/0 | 3142 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0001t0003 | 0/0 | 3140 | 13 | 12 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0001t0005 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0001t0006 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0002t0001 | 0/0 | 3141 | 105 | 2 | 23 | 63 | 4 | 13 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0003t0002 | 1/0 | 3142 | 76 | 22 | 15 | 31 | 2 | 5 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0003t0004 | 0/0 | 3142 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0004t0001 | 0/0 | 3141 | 5 | 5 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0005t0001 | 0/0 | 3141 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0006t0001 | 0/0 | 3141 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0001c0009t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0002c0007t0002 | 0/0 | 3142 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0003c0010t0001 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
a0004c0008t0001 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | copy fasta | chr11 | 4089799 | 4143932 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 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 | 2 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0317 | 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 |
a0001c0001t0001g0326 | 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 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0001t0006g0287 | 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 |
a0001c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 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 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0003 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0003t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0005t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0005t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0006t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0006t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0001c0009t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0002c0007t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0002c0007t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0003c0010t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
a0004c0008t0001g0322 | 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 | g0176 | EUR | GBR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0259 | 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 | g0226 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00438 | hp2 | a0001 | c0003 | t0002 | g0072 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00609 | hp1 | a0001 | c0003 | t0002 | g0030 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0094 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0087 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0186 | 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 | g0100 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01099 | hp1 | a0003 | c0010 | t0001 | g0275 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01192 | hp2 | a0001 | c0003 | t0002 | g0057 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0330 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01243 | hp2 | a0001 | c0003 | t0004 | g0268 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0193 | 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 | g0012 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01358 | hp1 | a0001 | c0003 | t0002 | g0043 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0267 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01496 | hp1 | a0001 | c0003 | t0002 | g0054 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0181 | EUR | IBS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0083 | 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 | g0336 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01934 | hp1 | a0001 | c0003 | t0002 | g0007 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01943 | hp2 | a0001 | c0003 | t0002 | g0055 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01978 | hp2 | a0001 | c0003 | t0002 | g0066 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01981 | hp1 | a0001 | c0003 | t0002 | g0056 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0220 | 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 | g0200 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0287 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02055 | hp1 | a0001 | c0005 | t0001 | g0323 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02071 | hp2 | a0001 | c0003 | t0002 | g0048 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0053 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02135 | hp1 | a0001 | c0003 | t0002 | g0062 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02148 | hp2 | a0001 | c0003 | t0002 | g0036 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0229 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02258 | hp2 | a0001 | c0003 | t0002 | g0082 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02273 | hp1 | a0001 | c0003 | t0002 | g0068 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02273 | hp2 | a0001 | c0003 | t0002 | g0044 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0035 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02451 | hp2 | a0001 | c0003 | t0002 | g0077 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02523 | hp2 | a0001 | c0003 | t0002 | g0045 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02572 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0157 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02615 | hp2 | a0001 | c0003 | t0002 | g0046 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0031 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02647 | hp1 | a0001 | c0005 | t0001 | g0321 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02647 | hp2 | a0002 | c0007 | t0002 | g0033 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0325 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02717 | hp2 | a0001 | c0006 | t0001 | g0300 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02723 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0339 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02886 | hp1 | a0002 | c0007 | t0002 | g0032 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02922 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0106 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0071 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0093 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03139 | hp1 | a0001 | c0003 | t0002 | g0328 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03139 | hp2 | a0001 | c0003 | t0002 | g0067 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03491 | hp1 | a0001 | c0003 | t0002 | g0078 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0114 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03516 | hp1 | a0001 | c0003 | t0002 | g0065 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0074 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0096 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03831 | hp1 | a0001 | c0003 | t0002 | g0086 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03831 | hp2 | a0001 | c0003 | t0002 | g0038 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0258 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0123 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03942 | hp2 | a0001 | c0003 | t0002 | g0034 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18522 | hp2 | a0004 | c0008 | t0001 | g0322 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0060 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0050 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0334 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18942 | hp2 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18943 | hp1 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18945 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0292 | 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 | g0252 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0225 | 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 | g0173 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18953 | hp1 | a0001 | c0003 | t0002 | g0301 | 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 | g0039 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18959 | hp1 | a0001 | c0003 | t0002 | g0061 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18963 | hp1 | a0001 | c0003 | t0002 | g0070 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0282 | 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 | g0194 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18970 | hp2 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18971 | hp1 | a0001 | c0003 | t0002 | g0081 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18981 | hp1 | a0001 | c0003 | t0002 | g0076 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0058 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18982 | hp2 | a0001 | c0009 | t0001 | g0266 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18984 | hp1 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0294 | 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 | g0239 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18992 | hp1 | a0001 | c0003 | t0002 | g0303 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18998 | hp2 | a0001 | c0003 | t0002 | g0075 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0246 | 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 | g0059 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19006 | hp2 | a0001 | c0003 | t0002 | g0302 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19011 | hp1 | a0001 | c0003 | t0002 | g0063 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19030 | hp1 | a0001 | c0006 | t0001 | g0272 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0231 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0235 | 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 | g0288 | 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 | g0041 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0167 | 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 | g0245 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19064 | hp2 | a0001 | c0003 | t0002 | g0042 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0023 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0141 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20805 | hp1 | a0001 | c0003 | t0002 | g0084 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | GIH | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | GIH | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0329 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG06807 | hp1 | a0001 | c0003 | t0002 | g0022 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0095 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0073 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0210 | REF | REF | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0079 | REF | REF | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
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 |
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 | a0001c0005a0004c0008 | 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 | a0001c0002a0001c0004 | 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 | a0001c0001a0001c0002a0001c0004others(5): Show | 289 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(286): 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 |
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 | a0001c0001t0005a0001c0003t0004 | 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 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(8): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(8): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(8): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*316C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 316 | chr11 | 4138699 |
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 | a0001c0001t0001g0340 | 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 | a0001c0001t0003g0339 | 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 | 259 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(256): Show | 280 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(277): 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0338 | 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 | a0001c0001t0003g0090 | 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 | 205 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(202): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): 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 | 307 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(304): Show | 328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.19+413G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095444 | ||||||
chr11:4095491
|
G | T | 36 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0234others(33): 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 | a0001c0001t0001g0069a0001c0001t0001g0233a0001c0001t0001g0304others(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 | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): 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 | a0001c0004t0001g0031 | 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 | a0001c0002t0001g0232 | 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 | a0001c0001t0002g0088 | 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 | a0001c0004t0001g0096 | 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 | 157 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(154): 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 | a0001c0002t0001g0232 | 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 | a0001c0004t0001g0031 | 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 | a0001c0002t0001g0008a0001c0002t0001g0097 | 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 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(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 | a0001c0004t0001g0023 | 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 | a0001c0001t0001g0234 | 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 | 89 | a0001c0001t0001g0133a0001c0002t0001g0001a0001c0002t0001g0002others(86): 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 | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(116): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): 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 | a0001c0001t0001g0184 | 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 | a0001c0003t0002g0068 | 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 | a0001c0001t0002g0088 | 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 | a0001c0003t0002g0025a0001c0003t0004g0268a0002c0007t0002g0032others(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 | a0001c0003t0002g0302a0001c0003t0002g0303 | 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 | a0001c0001t0003g0090a0001c0001t0003g0104 | 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 | a0001c0001t0003g0102a0001c0001t0003g0103 | 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 | a0001c0001t0003g0339 | 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 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0003g0330 | 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 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306 | 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 | 42 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(39): 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 | a0001c0001t0001g0069a0001c0001t0001g0105a0001c0001t0001g0185others(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 | 140 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(137): Show | 144 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(141): 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 | 46 | a0001c0001t0001g0234a0001c0001t0001g0257a0001c0001t0001g0265others(43): 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 | a0001c0003t0002g0087 | 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 | a0001c0003t0002g0067 | 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 | a0001c0006t0001g0272 | 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 | 33 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(30): 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 | 138 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 141 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(138): 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 | a0001c0001t0001g0107 | 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 | a0001c0003t0002g0086 | 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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0002t0001g0232 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0185 | 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 | 254 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 275 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(272): 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 | 319 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(316): Show | 340 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(337): 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 | a0001c0001t0005g0267 | 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 | a0001c0001t0001g0310a0001c0001t0001g0326a0001c0001t0001g0327 | 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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(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 | a0001c0002t0001g0232 | 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 | a0001c0002t0001g0125 | 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 | a0001c0001t0001g0257a0001c0002t0001g0126a0001c0002t0001g0232others(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 | 121 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(118): 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 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0246others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(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 | a0001c0001t0001g0091a0001c0001t0001g0192a0001c0001t0001g0233others(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 |
74 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0098others(71): Show | 77 | HG00423.hp1 HG00639.hp2 HG00642.hp2 others(74): 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 | a0001c0001t0001g0069a0001c0001t0001g0185a0001c0001t0001g0190others(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 | a0001c0001t0001g0338a0001c0006t0001g0272a0001c0006t0001g0300 | 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 | 41 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(38): 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 | 41 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(38): 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 | a0001c0002t0001g0121 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | 54 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(51): 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 | 128 | a0001c0001t0001g0011a0001c0001t0001g0105a0001c0001t0001g0107others(125): 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 | a0001c0001t0001g0017a0001c0001t0001g0019 | 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 | 3 | a0001c0003t0002g0022a0001c0003t0002g0094a0001c0003t0002g0095 | 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 | a0001c0003t0002g0004a0001c0003t0002g0074 | 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 | a0001c0001t0001g0219a0001c0001t0001g0230a0001c0001t0001g0296 | 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 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0127others(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 | 268 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(265): Show | 289 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(286): 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 | a0001c0001t0001g0311 | 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 | 34 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(31): 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 | a0001c0003t0002g0025 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0089a0001c0001t0001g0185a0001c0002t0001g0108others(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 | a0001c0004t0001g0023 | 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 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0003g0330 | 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 | 17 | a0001c0001t0001g0273a0001c0001t0001g0289a0001c0001t0001g0290others(14): 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 | a0001c0001t0001g0069a0001c0001t0001g0187a0001c0001t0001g0212others(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 | 38 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0099others(35): Show | 40 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(37): 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 | a0001c0001t0001g0012a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0001t0001g0332 | 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 | 311 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(308): Show | 332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): 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 | a0001c0004t0001g0096 | 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 | a0001c0002t0001g0155 | 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 | a0001c0003t0002g0073a0001c0003t0002g0087 | 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 | a0001c0002t0001g0097 | 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 | 125 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(122): 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 | a0001c0004t0001g0106 | 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 | 15 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0040others(12): 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 | a0001c0003t0002g0025 | 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 | a0001c0001t0003g0102a0001c0001t0003g0103 | 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 | a0001c0003t0002g0060 | 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 | a0001c0002t0001g0130 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0251a0001c0001t0001g0252 | 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 | 267 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.108+34C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102115 | ||||||
chr11:4102197
|
C | G | 89 | a0001c0001t0001g0133a0001c0002t0001g0001a0001c0002t0001g0002others(86): 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 | 34 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(31): 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 | a0001c0002t0001g0154 | 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 | 41 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(38): 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 | a0001c0003t0004g0268 | 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 | a0001c0003t0002g0093 | 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 | a0001c0001t0003g0090a0001c0001t0003g0102a0001c0001t0003g0103others(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 | 48 | a0001c0001t0001g0221a0001c0001t0001g0251a0001c0001t0001g0252others(45): 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 | a0001c0003t0002g0073a0001c0003t0002g0087 | 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 | 267 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): 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 | a0001c0002t0001g0153 | 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 | 129 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0098others(126): 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 | a0001c0004t0001g0096 | 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 | 83 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0099others(80): Show | 86 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(83): 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 | a0001c0002t0001g0124 | 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 | 34 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(31): 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 | a0001c0001t0001g0288 | 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 | 41 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(38): 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 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 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 | 42 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(39): 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 | a0001c0001t0005g0267 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | 131 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(128): 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 | 20 | a0001c0001t0001g0192a0001c0001t0001g0199a0001c0001t0001g0209others(17): Show | 20 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(17): 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 | a0001c0001t0002g0088a0001c0003t0002g0038a0001c0003t0002g0062others(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 | a0001c0001t0001g0098a0001c0001t0001g0185a0001c0001t0001g0188others(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 | 214 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): 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 | 34 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(31): 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 | a0001c0003t0002g0046 | 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 | 42 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(39): 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0002t0001g0173 | 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 | 42 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(39): 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 | a0001c0002t0001g0122 | 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 | 35 | a0001c0001t0001g0011a0001c0001t0001g0089a0001c0001t0001g0105others(32): 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 | a0001c0003t0002g0067 | 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0001t0005g0267 | 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 | a0001c0003t0004g0268 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0014 | 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 | 52 | a0001c0001t0001g0105a0001c0001t0001g0217a0001c0001t0001g0235others(49): 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 | 235 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 256 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(253): 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 | a0001c0001t0001g0013a0001c0001t0001g0069a0001c0001t0001g0194others(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 | a0001c0002t0001g0108a0001c0002t0001g0115a0001c0002t0001g0116others(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 | a0001c0003t0002g0067 | 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 | a0001c0001t0001g0216 | 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 | a0001c0003t0002g0025 | 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 | a0001c0003t0002g0065 | 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 | a0001c0001t0001g0195a0001c0001t0001g0200 | 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 | a0001c0002t0001g0159 | 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 | a0001c0003t0002g0231 | 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 | a0001c0006t0001g0300 | 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 | 43 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(40): 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 | 88 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(85): 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 | a0001c0002t0001g0123a0001c0002t0001g0126 | 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 | a0001c0004t0001g0024 | 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 | a0001c0004t0001g0031 | 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 | a0001c0001t0001g0234a0001c0004t0001g0023 | 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 | a0001c0004t0001g0024a0001c0004t0001g0031a0001c0004t0001g0106 | 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 | a0001c0001t0001g0189a0001c0002t0001g0008a0001c0002t0001g0097 | 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 | a0001c0001t0001g0105a0001c0004t0001g0023 | 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 | a0001c0001t0001g0312 | 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 | 9 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0251others(6): 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 | a0001c0001t0001g0247 | 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 | a0001c0004t0001g0096 | 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 | a0001c0004t0001g0024a0001c0004t0001g0031a0001c0004t0001g0106 | 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 | 148 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(145): 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 | a0001c0003t0002g0303 | 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 | a0001c0003t0002g0303 | 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 | a0001c0001t0001g0208a0001c0001t0001g0218 | 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 | 148 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(145): 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0003t0002g0303 | 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 | a0001c0003t0002g0303 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0003g0090a0001c0001t0003g0102a0001c0001t0003g0103others(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 | 149 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(146): 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 | a0001c0003t0002g0303 | 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 | a0001c0003t0002g0303 | 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | 42 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(39): 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 | a0001c0003t0002g0004a0001c0003t0002g0074 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0005g0267 | 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 | a0001c0003t0002g0004a0001c0003t0002g0074 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0201a0001c0001t0001g0209a0001c0001t0001g0221others(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 | 115 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(112): 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 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0236others(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 | 43 | a0001c0001t0001g0230a0001c0001t0001g0299a0001c0003t0002g0022others(40): 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 | a0001c0003t0002g0067 | 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 | 137 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(134): 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 | 42 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(39): 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 | a0001c0003t0002g0093 | 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 | a0001c0003t0002g0303 | 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 | a0001c0003t0002g0058 | 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | a0001c0001t0001g0243 | 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 | 94 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(91): 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 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0278others(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 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0029others(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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | a0001c0002t0001g0129 | 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 | 9 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0251others(6): 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 | a0001c0003t0002g0067 | 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021 | 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 | 152 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(149): 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 | 153 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(150): 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 | a0001c0001t0001g0256 | 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 | a0001c0002t0001g0137a0001c0002t0001g0138a0001c0002t0001g0182others(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 | 313 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(310): Show | 334 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(331): 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 | a0001c0001t0001g0251a0001c0001t0001g0278a0001c0001t0002g0088others(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 | a0001c0003t0002g0073a0001c0003t0002g0087 | 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 | a0001c0004t0001g0024a0001c0004t0001g0031a0001c0004t0001g0106 | 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 | a0001c0004t0001g0096 | 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 | a0001c0002t0001g0139 | 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 | a0001c0003t0002g0067 | 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 | a0001c0003t0002g0328a0001c0003t0002g0329 | 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 | 153 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(150): 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0003t0002g0057 | 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 | 50 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(47): 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | 264 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): 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 | a0001c0001t0001g0101a0001c0001t0001g0304a0001c0002t0001g0140others(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 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(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 | a0001c0002t0001g0161 | 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 | a0001c0003t0002g0334 | 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 | 153 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(150): 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0001t0003g0090 | 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 | 42 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(39): 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 | a0001c0001t0001g0224 | 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 | a0001c0003t0002g0039 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0249 | 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 | 191 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(188): 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 | 43 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(40): 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 | a0001c0002t0001g0128 | 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 | a0001c0001t0001g0260a0001c0001t0001g0265 | 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 | a0001c0001t0003g0090a0001c0001t0003g0102a0001c0001t0003g0103others(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 | a0001c0001t0001g0237a0001c0001t0001g0246 | 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 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(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 | a0001c0003t0002g0093 | 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 | a0001c0003t0002g0073a0001c0003t0002g0087 | 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 | a0001c0002t0001g0150 | 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 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019 | 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0193 | 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 | a0001c0004t0001g0024a0001c0004t0001g0031a0001c0004t0001g0106 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0098a0001c0001t0003g0020a0001c0002t0001g0115others(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 | a0001c0001t0005g0267 | 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 | a0001c0002t0001g0137a0001c0002t0001g0138a0001c0002t0001g0159others(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 | a0001c0001t0003g0330 | 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 | a0001c0003t0002g0073 | 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 | a0001c0003t0002g0073a0001c0003t0002g0087 | 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 | a0001c0003t0002g0067 | 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 | a0001c0001t0001g0202a0001c0001t0001g0228a0001c0001t0001g0233others(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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | 316 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(313): Show | 337 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(334): 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0277 | 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 | 87 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(84): 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 | a0001c0003t0002g0037a0001c0003t0002g0043a0001c0003t0002g0044others(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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | a0001c0001t0001g0273a0001c0001t0001g0278 | 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 | 87 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(84): 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 | a0001c0001t0001g0204 | 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 | 310 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(307): Show | 331 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(328): 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 | a0001c0003t0002g0085 | 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 | a0001c0001t0003g0339 | 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 | a0001c0002t0001g0232 | 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 | a0001c0003t0002g0231 | 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 | a0001c0006t0001g0272 | 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 | a0001c0004t0001g0096 | 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 | a0001c0006t0001g0229 | 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 | a0001c0004t0001g0096 | 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 | 47 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(44): 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 | 149 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(146): 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 | a0001c0004t0001g0031a0001c0004t0001g0106 | 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 | 118 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(115): Show | 121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): 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 | a0001c0001t0001g0091a0001c0001t0001g0092 | 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | a0001c0004t0001g0096 | 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 | a0001c0004t0001g0096 | 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 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(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 | a0001c0001t0001g0304 | 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 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(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 | 273 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(270): Show | 294 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(291): 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 | a0001c0004t0001g0096 | 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 | a0001c0006t0001g0272 | 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 | a0001c0001t0001g0282a0001c0001t0001g0294a0001c0001t0001g0295 | 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 | a0001c0003t0002g0035a0001c0003t0002g0036a0001c0003t0002g0054others(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 | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(116): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): 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 | a0001c0001t0001g0236 | 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 | 43 | a0001c0002t0001g0112a0001c0003t0002g0022a0001c0003t0002g0030others(40): 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 | a0001c0002t0001g0232 | 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 | a0001c0003t0002g0082 | 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 | a0001c0002t0001g0258 | 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 | 136 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(133): 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 | a0001c0001t0001g0219 | 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 | a0001c0004t0001g0096 | 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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | a0001c0001t0003g0090a0001c0001t0003g0102a0001c0001t0003g0103others(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 | a0001c0003t0002g0075a0001c0003t0002g0076a0001c0003t0002g0081 | 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 | a0001c0001t0001g0234 | 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 | a0001c0005t0001g0321 | 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 | a0001c0001t0001g0288 | 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 | a0001c0003t0002g0231 | 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 | a0001c0002t0001g0115 | 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 | a0001c0002t0001g0141a0001c0002t0001g0176a0001c0002t0001g0177others(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 | a0001c0003t0002g0231 | 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 | a0001c0003t0002g0039a0001c0003t0002g0053 | 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 | 42 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(39): 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 | a0001c0001t0001g0225 | 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 | 85 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0098others(82): Show | 88 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.877-765C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120839 | ||||||
chr11:4120942
|
C | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(116): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.877-662C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120942 | ||||||
chr11:4120999
|
G | A | 59 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(56): 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 | a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0002t0001g0149 | 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 | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(116): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): 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 | a0001c0003t0002g0004a0001c0003t0002g0074 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | a0001c0001t0001g0225 | 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 | 42 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(39): 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 | 42 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(39): 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 | a0001c0001t0005g0267 | 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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | a0001c0003t0002g0085 | 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 | 314 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.1118+242T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122462 | ||||||
chr11:4122491
|
G | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(113): Show | 119 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(116): 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 | a0001c0006t0001g0229 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(116): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.1118+436T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122656 | ||||||
chr11:4122760
|
C | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(116): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): 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 | a0001c0003t0002g0302a0001c0003t0002g0303 | 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 | 54 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(51): 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 | a0001c0003t0002g0093 | 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 | a0001c0001t0001g0288 | 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 | 9 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0251others(6): 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 | 271 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(268): Show | 292 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1320+228A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123612 | ||||||
chr11:4123637
|
C | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(116): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): 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 | a0001c0001t0005g0267 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0003t0002g0030others(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 | a0001c0003t0002g0093 | 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 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 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 | a0001c0001t0005g0267 | 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 | 88 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(85): 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 | 136 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(133): 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 | a0001c0001t0003g0016 | 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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | 88 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(85): 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 | a0001c0003t0002g0328a0001c0003t0002g0329 | 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 | a0001c0003t0002g0082 | 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 | a0001c0004t0001g0096 | 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 | 146 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(143): 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 | 92 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(89): 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 | 43 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(40): 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 | 92 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(89): 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 | 92 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(89): 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0203 | 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 | a0001c0003t0002g0039a0001c0003t0002g0053 | 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 | a0001c0001t0001g0312 | 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 | a0001c0002t0001g0112 | 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 | a0001c0002t0001g0112 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | 129 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(126): Show | 132 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(129): 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 | a0001c0003t0002g0093 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0001t0001g0234 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0001t0001g0233a0001c0001t0001g0313a0001c0001t0001g0314others(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 | a0001c0001t0001g0208a0001c0001t0001g0215a0001c0001t0001g0218 | 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 | a0001c0001t0003g0090a0001c0001t0003g0102a0001c0001t0003g0103others(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 | a0001c0004t0001g0106 | 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 | a0001c0001t0001g0234 | 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 | a0003c0010t0001g0275 | 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | 88 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(85): 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 | a0001c0004t0001g0096 | 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 | a0001c0004t0001g0023a0001c0004t0001g0024a0001c0004t0001g0031others(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 | a0001c0002t0001g0008a0001c0002t0001g0097 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | 84 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0098others(81): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0002t0001g0142 | 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 | a0001c0001t0001g0005a0001c0001t0001g0220a0001c0001t0001g0286others(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 | 80 | a0001c0001t0001g0069a0001c0001t0001g0212a0001c0001t0001g0233others(77): 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 | 44 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(41): 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | a0001c0004t0001g0096 | 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 | a0001c0003t0002g0025 | 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 | a0001c0002t0001g0259 | 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 | a0001c0001t0001g0283 | 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 | 43 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(40): 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 | 162 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(159): Show | 166 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(163): 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 | a0001c0001t0001g0014a0001c0001t0001g0187a0001c0001t0001g0219others(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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | a0001c0003t0002g0075a0001c0003t0002g0081 | 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 | 51 | a0001c0001t0001g0234a0001c0001t0002g0080a0001c0001t0002g0088others(48): 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 | a0001c0006t0001g0300 | 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 | a0001c0001t0001g0196 | 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 | a0001c0003t0002g0067 | 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | 88 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(85): 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 | 44 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(41): 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 | a0001c0006t0001g0272 | 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 | a0001c0002t0001g0175 | 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 | a0001c0002t0001g0183 | 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 | 53 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0009others(50): 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 | a0001c0002t0001g0008a0001c0002t0001g0026a0001c0002t0001g0097others(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 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0117others(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 | a0001c0002t0001g0124a0001c0002t0001g0141a0001c0002t0001g0151others(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 | a0001c0002t0001g0176 | 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 | a0001c0002t0001g0108 | 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 | a0001c0001t0001g0100 | 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 | 89 | a0001c0001t0001g0100a0001c0002t0001g0001a0001c0002t0001g0002others(86): 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 | a0001c0001t0001g0327 | 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 |
8 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0251others(5): 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 | a0001c0001t0001g0091a0001c0001t0001g0241a0001c0001t0001g0242others(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 | a0001c0001t0001g0105a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261others(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 |
35 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0187others(32): Show | 35 | HG00423.hp1 HG00639.hp2 HG00642.hp2 others(32): 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 | a0001c0001t0001g0186a0001c0001t0001g0307a0001c0001t0001g0308others(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 | a0001c0001t0001g0089a0001c0001t0001g0191a0001c0001t0001g0202others(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 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0279others(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 | a0001c0001t0001g0196a0001c0001t0001g0289a0001c0001t0001g0297others(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 | a0001c0001t0001g0069a0001c0001t0001g0184a0001c0001t0001g0205others(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 | a0001c0003t0002g0030a0001c0003t0002g0035a0001c0003t0002g0041others(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 | a0001c0001t0001g0304a0001c0003t0002g0038a0001c0003t0002g0057 | 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 | a0001c0003t0002g0065 | 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 | a0001c0001t0001g0305a0001c0003t0002g0303 | 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 | 4 | a0001c0003t0002g0022a0001c0003t0002g0094a0001c0003t0002g0095others(1): Show | 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 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0003t0002g0003others(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 | a0001c0001t0001g0333a0001c0001t0003g0320 | 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 | a0001c0001t0003g0319 | 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 | a0001c0001t0003g0318 | 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 | a0001c0001t0001g0233a0001c0001t0001g0315 | 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 | a0001c0003t0002g0094 | 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 | a0001c0001t0005g0267 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0324 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0003g0339 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0003g0090 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 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 | a0001c0001t0003g0016a0001c0001t0003g0021 | 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 | a0001c0001t0001g0327a0001c0003t0002g0006a0001c0003t0002g0071others(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 | a0001c0001t0001g0013a0001c0001t0001g0101 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(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 | a0001c0001t0001g0203a0001c0001t0001g0269a0001c0001t0001g0271others(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 | a0001c0001t0001g0133a0001c0001t0001g0185a0001c0001t0001g0288others(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 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0226others(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 | a0001c0001t0001g0306a0001c0003t0002g0044 | 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 | a0001c0003t0002g0334 | 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 | a0001c0003t0002g0022 | 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 | 221 | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0089others(218): Show | 239 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(236): 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 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(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 | 156 | a0001c0001t0001g0089a0001c0001t0001g0099a0001c0001t0001g0105others(153): 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 | a0001c0001t0001g0185a0001c0001t0001g0277a0001c0001t0001g0317others(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 | 106 | a0001c0001t0001g0105a0001c0001t0001g0195a0001c0001t0001g0213others(103): 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 | a0001c0001t0001g0317a0001c0002t0001g0173a0001c0003t0002g0044others(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 | 75 | a0001c0001t0001g0105a0001c0001t0001g0235a0001c0001t0001g0236others(72): 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 | a0001c0003t0002g0044 | 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 | a0001c0002t0001g0134a0001c0003t0002g0030a0001c0003t0002g0034others(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 | a0001c0003t0002g0044 | 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 | a0001c0003t0002g0030a0001c0003t0002g0035a0001c0003t0002g0036others(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 | 89 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(86): 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 | a0001c0001t0001g0234 | 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 | 42 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(39): 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 | a0001c0001t0001g0304 | 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 | 43 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(40): 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 | a0001c0006t0001g0229 | 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 | a0001c0002t0001g0134 | 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 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0186others(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 | a0001c0003t0002g0065 | 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 | a0001c0003t0002g0049 | 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 | a0001c0002t0001g0157 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093 | 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 | 270 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(267): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): 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 | a0001c0002t0001g0123 | 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 | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1770-984G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131302 | ||||||
chr11:4131386
|
G | A | 1 | a0001c0001t0001g0284 | 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 | a0001c0003t0002g0043 | 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 | a0001c0001t0003g0090a0001c0001t0003g0102a0001c0001t0003g0103others(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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | a0001c0002t0001g0132a0001c0002t0001g0140a0001c0002t0001g0179 | 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 | 129 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(126): Show | 132 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(129): 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 | a0001c0003t0002g0095 | 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 | 116 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(113): Show | 119 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(116): 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 | a0001c0001t0001g0216 | 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 | 84 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0098others(81): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1770-109C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4132177 | ||||||
chr11:4132178
|
A | G | 84 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0098others(81): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1770-108A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4132178 | ||||||
chr11:4132537
|
A | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): 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 | a0001c0009t0001g0266 | 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 | a0001c0002t0001g0125 | 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 | 89 | a0001c0001t0001g0248a0001c0002t0001g0001a0001c0002t0001g0002others(86): 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 | a0001c0001t0001g0234 | 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 | 88 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0008others(85): 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 | 312 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(309): Show | 333 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(330): 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 | a0001c0003t0002g0006a0001c0003t0002g0071a0001c0003t0002g0082 | 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 | a0001c0003t0002g0085 | 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0004t0001g0096 | 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 | 99 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0099others(96): Show | 103 | HG00408.hp2 HG00558.hp1 HG00639.hp2 others(100): 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 | 107 | a0001c0001t0001g0098a0001c0001t0001g0133a0001c0001t0001g0198others(104): 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 | a0001c0001t0001g0069a0001c0001t0001g0305a0001c0001t0001g0310others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(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 | a0001c0001t0001g0013a0001c0001t0001g0089a0001c0001t0001g0091others(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 |
8 | a0001c0001t0001g0107a0001c0001t0001g0253a0001c0001t0001g0254others(5): 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 | a0001c0001t0001g0011a0001c0001t0001g0185a0001c0001t0001g0251others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0333 | 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 | a0001c0003t0002g0085 | 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0003g0318a0001c0001t0003g0319a0001c0001t0003g0320others(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 | a0001c0004t0001g0096 | 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 | 115 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(112): Show | 118 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.2002-272T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134810 | ||||||
chr11:4134876
|
G | A | 94 | a0001c0001t0001g0234a0001c0002t0001g0001a0001c0002t0001g0002others(91): 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0001t0001g0234 | 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 | 128 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): 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 | a0001c0003t0002g0073 | 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 | 84 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0098others(81): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0185 | 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 | a0001c0002t0001g0162 | 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 | a0001c0004t0001g0024 | 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 | a0001c0003t0002g0073a0001c0003t0002g0087a0001c0003t0002g0231others(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 | a0001c0003t0002g0328 | 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 | a0001c0003t0002g0328 | 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 | a0001c0003t0002g0328 | 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 | a0001c0003t0002g0328 | 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 | a0001c0003t0002g0004a0001c0003t0002g0074a0001c0003t0002g0077 | 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 | 267 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): 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 | a0001c0001t0005g0267 | 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 | a0001c0003t0002g0067a0001c0004t0001g0096 | 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 | a0001c0004t0001g0023 | 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 | a0001c0003t0004g0268a0002c0007t0002g0032a0002c0007t0002g0033 | 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 | 259 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(256): Show | 280 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(277): 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | a0001c0001t0001g0069a0001c0001t0001g0304a0001c0001t0001g0305others(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 | a0001c0001t0001g0069a0001c0001t0001g0304a0001c0001t0001g0305others(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 | a0001c0001t0001g0069a0001c0001t0001g0304a0001c0001t0001g0305others(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 | a0001c0001t0001g0069a0001c0001t0001g0304a0001c0001t0001g0305others(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 | a0001c0001t0001g0234 | 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 | 115 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(112): Show | 118 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.2191-1399A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136796 | ||||||
chr11:4136806
|
G | A | 44 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(41): 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2191-1295G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136900 | ||||||
chr11:4136915
|
G | A | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2191-1280G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136915 | ||||||
chr11:4136922
|
C | T | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2191-1273C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136922 | ||||||
chr11:4136977
|
G | C | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | 115 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(112): Show | 118 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(115): 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 | a0001c0001t0005g0267 | 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 | a0001c0002t0001g0163 | 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 | 325 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 349 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(346): 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 | a0001c0001t0001g0338 | 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 | a0001c0003t0002g0302 | 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 | a0001c0003t0002g0302 | 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 | a0001c0003t0002g0038 | 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 | 44 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(41): 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 | a0001c0001t0005g0267 | 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 | a0001c0001t0001g0284a0001c0001t0001g0285 | 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 | 128 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0069others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): 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 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(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 | 267 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): 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 | a0001c0003t0002g0302 | 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 | 318 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(315): Show | 339 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.2191-705C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137490 | ||||||
chr11:4137509
|
C | T | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0002t0001g0146 | 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0003t0002g0302 | 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 | a0001c0003t0002g0030a0001c0003t0002g0034a0001c0003t0002g0035others(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 | a0001c0003t0002g0302 | 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2191-623G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137572 | ||||||
chr11:4137574
|
G | A | 42 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(39): 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2191-614G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137581 | ||||||
chr11:4137582
|
G | A | 138 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(135): 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 | a0001c0004t0001g0096 | 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 | a0001c0003t0002g0093 | 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 | a0001c0002t0001g0151 | 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2191-578T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137617 | ||||||
chr11:4137618
|
G | T | 265 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-577G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137618 | ||||||
chr11:4137628
|
T | C | 265 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): 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 | a0001c0001t0001g0107a0001c0001t0001g0187a0001c0001t0001g0280others(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 | 253 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(250): Show | 274 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(271): 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 | a0001c0002t0001g0029 | 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 | a0001c0002t0001g0029 | 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 | 43 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(40): 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | a0001c0003t0002g0328a0001c0003t0002g0329 | 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 | a0001c0001t0001g0107a0001c0001t0001g0187a0001c0001t0001g0280others(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 | a0001c0003t0002g0025a0001c0003t0002g0093 | 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 | 82 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0098others(79): Show | 85 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(82): 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 | a0001c0002t0001g0179 | 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 | a0001c0003t0002g0025a0001c0003t0002g0093 | 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 | 265 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): 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 | a0001c0003t0002g0025a0001c0003t0002g0093a0001c0003t0004g0268others(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 | 265 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-200A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137995 | ||||||
chr11:4138017
|
G | A | 265 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-178G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138017 | ||||||
chr11:4138022
|
C | T | 43 | a0001c0003t0002g0022a0001c0003t0002g0030a0001c0003t0002g0034others(40): 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 | 313 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(310): Show | 334 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(331): 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 | a0001c0001t0001g0069a0001c0001t0001g0195a0001c0001t0001g0233others(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 | a0001c0001t0001g0269a0001c0001t0001g0277a0001c0001t0001g0283 | 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 |
224 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(221): Show | 245 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(242): 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 | a0001c0001t0001g0187a0001c0001t0001g0194 | 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 | a0001c0004t0001g0024 | 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 | 228 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(225): Show | 249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): 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 | a0001c0001t0001g0069a0001c0001t0001g0233a0001c0001t0001g0304others(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 | a0001c0001t0003g0318a0001c0001t0003g0319a0001c0001t0003g0320 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0133 | 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 | 266 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): 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 | a0001c0001t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2191-54T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138141 |