geneid | 91869 |
---|---|
ensemblid | ENSG00000163933.10 |
hgncid | 30220 |
symbol | RFT1 |
name | RFT1 homolog |
refseq_nuc | NM_052859.4 |
refseq_prot | NP_443091.1 |
ensembl_nuc | ENST00000296292.8 |
ensembl_prot | ENSP00000296292.3 |
mane_status | MANE Select |
chr | chr3 |
start | 53088483 |
end | 53130435 |
strand | - |
ver | v1.2 |
region | chr3:53088483-53130435 |
region5000 | chr3:53083483-53135435 |
regionname0 | RFT1_chr3_53088483_53130435 |
regionname5000 | RFT1_chr3_53083483_53135435 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 541 | 300 | 72 | 66 | 107 | 12 | 41 | 72 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0002 | 0/0 | 541 | 18 | 17 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0003 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0004 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0005 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0006 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0007 | 0/0 | 371 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0008 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1626 | 168 | 62 | 29 | 43 | 7 | 25 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0002 | 0/0 | 1626 | 131 | 10 | 36 | 64 | 5 | 16 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0003 | 0/0 | 1626 | 18 | 17 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0004 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0005 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0006 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0007 | 0/0 | 1520 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0008 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0009 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
c0010 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3456 | 130 | 9 | 34 | 66 | 5 | 16 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0002 | 0/0 | 3456 | 52 | 23 | 8 | 16 | 1 | 4 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0003 | 0/1 | 3456 | 49 | 1 | 12 | 23 | 6 | 6 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0004 | 0/0 | 3456 | 21 | 0 | 5 | 2 | 0 | 14 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0005 | 1/0 | 3456 | 20 | 15 | 4 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0006 | 0/0 | 3456 | 15 | 15 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0007 | 0/0 | 3456 | 14 | 14 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0008 | 0/0 | 3456 | 5 | 4 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0009 | 0/0 | 3456 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0010 | 0/0 | 3456 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0011 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0012 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0013 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0014 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0015 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0016 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0017 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0018 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0019 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0020 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0021 | 0/0 | 3456 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0022 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0023 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
t0024 | 0/0 | 3456 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0002 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0003 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0004 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0007 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0014 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1626 | 168 | 62 | 29 | 43 | 7 | 25 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0002 | 0/0 | 1626 | 131 | 10 | 36 | 64 | 5 | 16 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0010 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0002c0003 | 0/0 | 1626 | 18 | 17 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0003c0004 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0004c0005 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0005c0009 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0006c0008 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0007c0007 | 0/0 | 1520 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0008c0006 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5081 | 52 | 23 | 8 | 16 | 1 | 4 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0003 | 0/1 | 5081 | 49 | 1 | 12 | 23 | 6 | 6 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0004 | 0/0 | 5081 | 20 | 0 | 5 | 2 | 0 | 13 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0005 | 1/0 | 5081 | 13 | 9 | 3 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0006 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0007 | 0/0 | 5081 | 14 | 14 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0008 | 0/0 | 5081 | 5 | 4 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0009 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0011 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0012 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0013 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0014 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0015 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0016 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0017 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0018 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0019 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0001t0020 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0002t0001 | 0/0 | 5081 | 125 | 9 | 32 | 63 | 5 | 16 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0002t0010 | 0/0 | 5081 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0002t0021 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0002t0022 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0002t0023 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0002t0024 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0001c0010t0001 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0002c0003t0005 | 0/0 | 5081 | 7 | 6 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0002c0003t0006 | 0/0 | 5081 | 11 | 11 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0003c0004t0001 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0004c0005t0001 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0005c0009t0001 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0006c0008t0001 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0007c0007t0004 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
a0008c0006t0006 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | copy fasta | chr3 | 53083483 | 53135435 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0002 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0014 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0005g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0008g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0008g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0014g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0015g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0018g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0019g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0001t0020g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0001 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0003 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0010g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0021g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0022g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0023g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0002t0024g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0001c0010t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0005g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0002c0003t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0003c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0004c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0005c0009t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0006c0008t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0007c0007t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
a0008c0006t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0066 | EUR | GBR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0248 | EUR | GBR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0192 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0044 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0247 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0074 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00438 | hp2 | a0005 | c0009 | t0001 | g0084 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00558 | hp2 | a0001 | c0001 | t0013 | g0068 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0060 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0237 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01109 | hp1 | a0002 | c0003 | t0005 | g0229 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01167 | hp1 | a0001 | c0002 | t0010 | g0113 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01168 | hp1 | a0001 | c0002 | t0021 | g0168 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01169 | hp2 | a0001 | c0002 | t0010 | g0114 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01175 | hp2 | a0001 | c0002 | t0024 | g0186 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01346 | hp2 | a0001 | c0010 | t0001 | g0215 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0064 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0207 | EUR | IBS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01884 | hp2 | a0002 | c0003 | t0005 | g0089 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01891 | hp2 | a0001 | c0001 | t0017 | g0154 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02129 | hp1 | a0001 | c0001 | t0019 | g0177 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02145 | hp1 | a0001 | c0002 | t0023 | g0172 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CDX | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | CDX | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0254 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0053 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02300 | hp2 | a0004 | c0005 | t0001 | g0116 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02572 | hp2 | a0001 | c0001 | t0016 | g0048 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0141 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02622 | hp1 | a0002 | c0003 | t0006 | g0035 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0086 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02630 | hp2 | a0002 | c0003 | t0006 | g0221 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02647 | hp1 | a0001 | c0001 | t0018 | g0080 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0151 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0098 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0239 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0249 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0169 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02818 | hp2 | a0008 | c0006 | t0006 | g0232 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02922 | hp1 | a0002 | c0003 | t0005 | g0036 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02976 | hp1 | a0002 | c0003 | t0006 | g0111 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03041 | hp1 | a0002 | c0003 | t0006 | g0220 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0088 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03139 | hp1 | a0002 | c0003 | t0006 | g0225 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0258 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03225 | hp1 | a0001 | c0001 | t0015 | g0152 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03516 | hp2 | a0002 | c0003 | t0006 | g0227 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03704 | hp1 | a0001 | c0001 | t0014 | g0214 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0206 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0093 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG03942 | hp2 | a0001 | c0001 | t0011 | g0112 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0094 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0095 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0139 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18941 | hp1 | a0001 | c0002 | t0022 | g0196 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18961 | hp2 | a0003 | c0004 | t0001 | g0038 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19012 | hp2 | a0006 | c0008 | t0001 | g0202 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19030 | hp1 | a0002 | c0003 | t0006 | g0222 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19240 | hp1 | a0002 | c0003 | t0005 | g0228 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA19240 | hp2 | a0002 | c0003 | t0006 | g0223 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20129 | hp1 | a0002 | c0003 | t0006 | g0226 | AFR | ASW | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ASW | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0197 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0131 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20905 | hp1 | a0007 | c0007 | t0004 | g0103 | SAS | GIH | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | GIH | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02486 | hp1 | a0002 | c0003 | t0005 | g0231 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02486 | hp2 | a0002 | c0003 | t0006 | g0224 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG02559 | hp2 | a0002 | c0003 | t0005 | g0036 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | USA | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
HG06807 | hp2 | a0002 | c0003 | t0005 | g0230 | AFR | USA | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
NA21309 | hp2 | a0002 | c0003 | t0006 | g0035 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0014 | REF | REF | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0236 | REF | REF | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:53098541
|
GCCTGTAA others(1177): Show |
G | 1 | a0007 | 1 | NA20905.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1103-239_1208+839d others(2): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/13 | chr3 | 53098541 | ||||||
chr3:53099456
|
T | C | 1 | a0006 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1133A>G | p.Tyr378Cys | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/13 | 1168/5081 | 1133/1626 | 378/541 | chr3 | 53099456 | ||
chr3:53099471
|
C | T | 1 | a0008 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1118G>A | p.Arg373His | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/13 | 1153/5081 | 1118/1626 | 373/541 | chr3 | 53099471 | ||
chr3:53119948
|
G | A | 1 | a0005 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.632C>T | p.Thr211Ile | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/13 | 667/5081 | 632/1626 | 211/541 | chr3 | 53119948 | ||
chr3:53121704
|
C | T | 2 | a0002a0008 | 19 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(16): Show |
missense_variant | MODERATE | c.553G>A | p.Ala185Thr | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/13 | 588/5081 | 553/1626 | 185/541 | chr3 | 53121704 | ||
chr3:53122390
|
A | T | 1 | a0004 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.440T>A | p.Met147Lys | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/13 | 475/5081 | 440/1626 | 147/541 | chr3 | 53122390 | ||
chr3:53130378
|
C | T | 1 | a0003 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.23G>A | p.Gly8Asp | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/13 | 58/5081 | 23/1626 | 8/541 | chr3 | 53130378 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:53091906
|
T | C | 6 | a0001c0002a0001c0010a0003c0004others(3): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
synonymous_variant | LOW | c.1623A>G | p.Thr541Thr | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1658/5081 | 1623/1626 | 541/541 | chr3 | 53091906 | ||
chr3:53122527
|
G | C | 1 | a0001c0010 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.303C>G | p.Gly101Gly | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/13 | 338/5081 | 303/1626 | 101/541 | chr3 | 53122527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:53088550
|
A | G | 1 | a0001c0001t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3353T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 3353 | chr3 | 53088550 | |||||
chr3:53088664
|
T | C | 1 | a0001c0002t0023 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3239A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 3239 | chr3 | 53088664 | |||||
chr3:53088708
|
C | G | 1 | a0001c0002t0022 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3195G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 3195 | chr3 | 53088708 | |||||
chr3:53088953
|
G | A | 11 | a0001c0002t0001a0001c0002t0010a0001c0002t0021others(8): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2950C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2950 | chr3 | 53088953 | |||||
chr3:53089016
|
C | T | 23 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(20): Show | 223 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*2887G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2887 | chr3 | 53089016 | |||||
chr3:53089063
|
A | T | 9 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(6): Show | 65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2840T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2840 | chr3 | 53089063 | |||||
chr3:53089083
|
C | T | 1 | a0001c0002t0010 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2820G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2820 | chr3 | 53089083 | |||||
chr3:53089197
|
G | A | 1 | a0001c0002t0021 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2706C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2706 | chr3 | 53089197 | |||||
chr3:53089248
|
A | G | 3 | a0001c0001t0004a0001c0001t0011a0007c0007t0004 | 22 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2655T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2655 | chr3 | 53089248 | |||||
chr3:53089257
|
A | G | 11 | a0001c0002t0001a0001c0002t0010a0001c0002t0021others(8): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2646T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2646 | chr3 | 53089257 | |||||
chr3:53089446
|
T | C | 1 | a0001c0002t0024 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2457A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2457 | chr3 | 53089446 | |||||
chr3:53089470
|
G | A | 11 | a0001c0002t0001a0001c0002t0010a0001c0002t0021others(8): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2433C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2433 | chr3 | 53089470 | |||||
chr3:53089537
|
A | T | 1 | a0001c0001t0014 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2366T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2366 | chr3 | 53089537 | |||||
chr3:53089623
|
A | T | 1 | a0001c0001t0013 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2280T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2280 | chr3 | 53089623 | |||||
chr3:53089738
|
A | G | 1 | a0001c0002t0021 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2165 | chr3 | 53089738 | |||||
chr3:53089928
|
G | A | 1 | a0001c0001t0007 | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1975C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1975 | chr3 | 53089928 | |||||
chr3:53090099
|
G | A | 3 | a0001c0001t0006a0002c0003t0006a0008c0006t0006 | 15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1804C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1804 | chr3 | 53090099 | |||||
chr3:53090100
|
A | T | 3 | a0001c0001t0006a0002c0003t0006a0008c0006t0006 | 15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1803T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1803 | chr3 | 53090100 | |||||
chr3:53090210
|
C | T | 1 | a0001c0001t0016 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1693G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1693 | chr3 | 53090210 | |||||
chr3:53090217
|
G | A | 1 | a0001c0001t0019 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1686 | chr3 | 53090217 | |||||
chr3:53090370
|
C | T | 2 | a0001c0001t0004a0007c0007t0004 | 21 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1533G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1533 | chr3 | 53090370 | |||||
chr3:53090771
|
A | G | 1 | a0001c0001t0017 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1132 | chr3 | 53090771 | |||||
chr3:53090894
|
C | T | 1 | a0001c0001t0008 | 5 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1009G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1009 | chr3 | 53090894 | |||||
chr3:53091023
|
G | C | 1 | a0001c0001t0020 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 880 | chr3 | 53091023 | |||||
chr3:53091104
|
A | T | 1 | a0001c0001t0016 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 799 | chr3 | 53091104 | |||||
chr3:53091281
|
G | C | 10 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(7): Show | 65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 622 | chr3 | 53091281 | |||||
chr3:53091413
|
A | T | 2 | a0001c0001t0003a0001c0001t0013 | 50 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*490T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 490 | chr3 | 53091413 | |||||
chr3:53091453
|
G | A | 18 | a0001c0001t0002a0001c0001t0008a0001c0001t0016others(15): Show | 198 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 450 | chr3 | 53091453 | |||||
chr3:53091552
|
A | G | 1 | a0001c0001t0012 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 351 | chr3 | 53091552 | |||||
chr3:53091569
|
T | C | 11 | a0001c0002t0001a0001c0002t0010a0001c0002t0021others(8): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*334A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 334 | chr3 | 53091569 | |||||
chr3:53091663
|
A | G | 1 | a0001c0001t0011 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 240 | chr3 | 53091663 | |||||
chr3:53091757
|
G | A | 3 | a0001c0001t0006a0002c0003t0006a0008c0006t0006 | 15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 146 | chr3 | 53091757 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:53092127
|
G | A | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(104): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1459-57C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 12/12 | chr3 | 53092127 | ||||||
chr3:53092210
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1459-140G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 12/12 | chr3 | 53092210 | ||||||
chr3:53092656
|
TTGCCCTG others(8): Show |
T | 51 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1209-53_1209-39del others(15): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092656 | ||||||
chr3:53092704
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1209-86G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092704 | ||||||
chr3:53092731
|
C | G | 1 | a0001c0002t0001g0120 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1209-113G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092731 | ||||||
chr3:53092778
|
C | T | 1 | a0001c0002t0001g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1209-160G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092778 | ||||||
chr3:53092900
|
A | C | 1 | a0001c0002t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1209-282T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092900 | ||||||
chr3:53093006
|
C | A | 5 | a0001c0001t0005g0023a0001c0001t0005g0086a0001c0001t0005g0134others(2): Show | 6 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-388G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093006 | ||||||
chr3:53093119
|
AC | A | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(104): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1209-502delG | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093119 | ||||||
chr3:53093189
|
C | A | 1 | a0001c0001t0007g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1209-571G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093189 | ||||||
chr3:53093268
|
A | C | 6 | a0001c0001t0005g0023a0001c0001t0005g0086a0001c0001t0005g0134others(3): Show | 7 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209-650T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093268 | ||||||
chr3:53093280
|
A | G | 1 | a0001c0002t0001g0184 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1209-662T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093280 | ||||||
chr3:53093499
|
C | A | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1209-881G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093499 | ||||||
chr3:53093524
|
G | A | 1 | a0001c0001t0016g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1209-906C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093524 | ||||||
chr3:53093599
|
C | A | 1 | a0001c0002t0001g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1209-981G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093599 | ||||||
chr3:53093657
|
G | C | 20 | a0001c0001t0002g0010a0001c0001t0002g0049a0001c0001t0002g0148others(17): Show | 22 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1209-1039C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093657 | ||||||
chr3:53093661
|
G | T | 104 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(101): Show | 132 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1209-1043C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093661 | ||||||
chr3:53093751
|
T | C | 51 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1209-1133A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093751 | ||||||
chr3:53093759
|
A | T | 1 | a0001c0001t0005g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1209-1141T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093759 | ||||||
chr3:53093860
|
A | G | 22 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(19): Show | 32 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1209-1242T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093860 | ||||||
chr3:53094184
|
G | C | 1 | a0001c0001t0020g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1209-1566C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094184 | ||||||
chr3:53094264
|
C | G | 1 | a0001c0001t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1209-1646G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094264 | ||||||
chr3:53094269
|
A | G | 1 | a0001c0001t0003g0079 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1209-1651T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094269 | ||||||
chr3:53094304
|
T | C | 2 | a0001c0001t0003g0067a0001c0001t0003g0071 | 2 | HG00733.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1209-1686A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094304 | ||||||
chr3:53094335
|
G | A | 51 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1209-1717C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094335 | ||||||
chr3:53094349
|
A | ACG | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0090others(1): Show | 6 | HG01993.hp2 HG02004.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-1733_1209-173 others(6): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094349 | ||||||
chr3:53094351
|
G | GCA | 4 | a0001c0001t0005g0023a0001c0001t0005g0086a0001c0001t0005g0150others(1): Show | 5 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1209-1735_1209-173 others(6): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | ||||||
chr3:53094351
|
GCA | G | 7 | a0001c0001t0003g0008a0001c0001t0003g0044a0001c0001t0003g0054others(4): Show | 10 | HG00280.hp2 HG00673.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1209-1735_1209-173 others(6): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | ||||||
chr3:53094351
|
GCACA | G | 56 | a0001c0001t0002g0010a0001c0001t0002g0148a0001c0001t0002g0162others(53): Show | 73 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1209-1737_1209-173 others(8): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | ||||||
chr3:53094351
|
GCACACA | G | 56 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(53): Show | 68 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1209-1739_1209-173 others(10): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | ||||||
chr3:53094351
|
GCACACAC others(1): Show |
G | 7 | a0001c0001t0003g0043a0001c0002t0001g0021a0001c0002t0001g0121others(4): Show | 8 | HG01243.hp2 HG01256.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1209-1741_1209-173 others(12): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | ||||||
chr3:53094351
|
GCACACAC others(3): Show |
G | 100 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(97): Show | 128 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1209-1743_1209-173 others(14): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | ||||||
chr3:53094353
|
A | G | 13 | a0001c0001t0004g0024a0001c0001t0004g0085a0001c0001t0004g0091others(10): Show | 14 | HG00673.hp1 HG02698.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1209-1735T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094353 | ||||||
chr3:53094355
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1209-1737T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094355 | ||||||
chr3:53094357
|
A | G | 2 | a0001c0001t0005g0028a0001c0001t0012g0169 | 3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1209-1739T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094357 | ||||||
chr3:53094359
|
A | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0148a0001c0001t0002g0162others(6): Show | 11 | HG01934.hp1 HG02451.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209-1741T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094359 | ||||||
chr3:53094361
|
A | G | 51 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(48): Show | 65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1209-1743T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094361 | ||||||
chr3:53094363
|
A | G | 7 | a0001c0001t0002g0149a0001c0001t0002g0158a0001c0001t0002g0159others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1209-1745T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094363 | ||||||
chr3:53094412
|
C | A | 1 | a0001c0002t0001g0184 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1209-1794G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094412 | ||||||
chr3:53094790
|
G | A | 1 | a0001c0001t0002g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1209-2172C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094790 | ||||||
chr3:53095024
|
TTGGGAGG others(99): Show |
T | 1 | a0001c0002t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1209-2512_1209-240 others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095024 | ||||||
chr3:53095050
|
G | A | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1209-2432C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095050 | ||||||
chr3:53095167
|
G | A | 51 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(48): Show | 64 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1209-2549C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095167 | ||||||
chr3:53095508
|
T | TG | 18 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0024others(15): Show | 21 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1209-2891dupC | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095508 | ||||||
chr3:53095514
|
C | G | 5 | a0001c0001t0005g0023a0001c0001t0005g0086a0001c0001t0005g0134others(2): Show | 6 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-2896G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095514 | ||||||
chr3:53095519
|
C | T | 1 | a0001c0001t0020g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1209-2901G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095519 | ||||||
chr3:53095695
|
G | A | 18 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0024others(15): Show | 21 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1209-3077C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095695 | ||||||
chr3:53095725
|
TA | T | 223 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(220): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1209-3108delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095725 | ||||||
chr3:53095876
|
C | A | 2 | a0001c0001t0005g0028a0001c0001t0012g0169 | 3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1209-3258G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095876 | ||||||
chr3:53096383
|
T | TA | 22 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(19): Show | 32 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1208+2997dupT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096383 | ||||||
chr3:53096419
|
C | T | 51 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1208+2962G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096419 | ||||||
chr3:53096422
|
C | T | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1208+2959G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096422 | ||||||
chr3:53096424
|
A | G | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1208+2957T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096424 | ||||||
chr3:53096450
|
G | A | 51 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1208+2931C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096450 | ||||||
chr3:53096461
|
C | T | 1 | a0001c0002t0001g0252 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1208+2920G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096461 | ||||||
chr3:53096701
|
A | G | 1 | a0001c0002t0001g0195 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1208+2680T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096701 | ||||||
chr3:53096729
|
T | C | 53 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 67 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1208+2652A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096729 | ||||||
chr3:53096754
|
A | C | 2 | a0001c0001t0005g0028a0001c0001t0012g0169 | 3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1208+2627T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096754 | ||||||
chr3:53096889
|
C | T | 51 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(48): Show | 65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1208+2492G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096889 | ||||||
chr3:53096897
|
C | A | 107 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(104): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1208+2484G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096897 | ||||||
chr3:53096908
|
C | A | 20 | a0001c0001t0002g0010a0001c0001t0002g0049a0001c0001t0002g0148others(17): Show | 22 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1208+2473G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096908 | ||||||
chr3:53097027
|
G | C | 22 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(19): Show | 32 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1208+2354C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097027 | ||||||
chr3:53097035
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1208+2346C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097035 | ||||||
chr3:53097040
|
C | T | 1 | a0001c0001t0017g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1208+2341G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097040 | ||||||
chr3:53097252
|
A | G | 1 | a0001c0001t0005g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1208+2129T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097252 | ||||||
chr3:53097257
|
C | T | 1 | a0001c0001t0002g0032 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1208+2124G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097257 | ||||||
chr3:53097261
|
G | A | 5 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0139others(2): Show | 7 | HG01069.hp2 HG01071.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208+2120C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097261 | ||||||
chr3:53097427
|
T | C | 1 | a0001c0001t0003g0081 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1208+1954A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097427 | ||||||
chr3:53097458
|
A | G | 1 | a0001c0001t0020g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1208+1923T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097458 | ||||||
chr3:53097505
|
T | C | 1 | a0001c0002t0001g0210 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1208+1876A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097505 | ||||||
chr3:53097725
|
T | C | 1 | a0001c0002t0001g0132 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1208+1656A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097725 | ||||||
chr3:53097756
|
T | C | 105 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(102): Show | 134 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1208+1625A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097756 | ||||||
chr3:53097813
|
T | C | 105 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(102): Show | 134 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1208+1568A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097813 | ||||||
chr3:53097814
|
G | A | 105 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(102): Show | 134 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1208+1567C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097814 | ||||||
chr3:53097932
|
A | G | 51 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(48): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1208+1449T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097932 | ||||||
chr3:53097933
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1208+1448C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097933 | ||||||
chr3:53098080
|
G | A | 2 | a0001c0001t0005g0086a0001c0001t0005g0161 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1208+1301C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098080 | ||||||
chr3:53098355
|
C | G | 54 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(51): Show | 69 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1208+1026G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098355 | ||||||
chr3:53098356
|
A | T | 54 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(51): Show | 69 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1208+1025T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098356 | ||||||
chr3:53098357
|
A | C | 54 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(51): Show | 69 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1208+1024T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098357 | ||||||
chr3:53098409
|
G | A | 2 | a0001c0002t0001g0252a0001c0002t0001g0253 | 2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1208+972C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098409 | ||||||
chr3:53098427
|
T | TGAGACAC others(13): Show |
25 | a0001c0001t0002g0010a0001c0001t0002g0049a0001c0001t0002g0104others(22): Show | 27 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.1208+934_1208+953d others(22): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098427 | ||||||
chr3:53098524
|
T | C | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1208+857A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098524 | ||||||
chr3:53098530
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1208+851G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098530 | ||||||
chr3:53098540
|
T | C | 17 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0070others(14): Show | 20 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1208+841A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098540 | ||||||
chr3:53098573
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1208+808G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098573 | ||||||
chr3:53098587
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1208+794C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098587 | ||||||
chr3:53098598
|
C | G | 1 | a0001c0002t0001g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1208+783G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098598 | ||||||
chr3:53098598
|
C | T | 1 | a0001c0002t0001g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1208+783G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098598 | ||||||
chr3:53098606
|
A | T | 121 | a0001c0001t0002g0011a0001c0001t0002g0045a0001c0001t0002g0162others(118): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1208+775T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098606 | ||||||
chr3:53098614
|
G | A | 5 | a0001c0001t0002g0178a0001c0002t0001g0141a0001c0002t0001g0200others(2): Show | 5 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+767C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098614 | ||||||
chr3:53098703
|
G | A | 1 | a0002c0003t0005g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1208+678C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098703 | ||||||
chr3:53098799
|
C | T | 2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1208+582G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098799 | ||||||
chr3:53098801
|
C | CA | 44 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(41): Show | 60 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1208+579dupT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | ||||||
chr3:53098801
|
C | CAA | 133 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0153others(130): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1208+578_1208+579d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | ||||||
chr3:53098801
|
C | CAAA | 20 | a0001c0001t0002g0106a0001c0001t0002g0190a0001c0001t0003g0057others(17): Show | 21 | HG00423.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1208+577_1208+579d others(5): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | ||||||
chr3:53098801
|
CA | C | 12 | a0001c0001t0006g0155a0001c0001t0006g0233a0001c0001t0006g0234others(9): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1208+579delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | ||||||
chr3:53098823
|
A | G | 13 | a0001c0001t0002g0010a0001c0001t0002g0148a0001c0001t0002g0149others(10): Show | 16 | HG01934.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1208+558T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098823 | ||||||
chr3:53098863
|
A | C | 1 | a0001c0002t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1208+518T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098863 | ||||||
chr3:53099052
|
G | A | 1 | a0008c0006t0006g0232 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1208+329C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53099052 | ||||||
chr3:53099133
|
C | G | 109 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(106): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1208+248G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53099133 | ||||||
chr3:53099362
|
T | C | 3 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0102 | 3 | HG03491.hp2 HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1208+19A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53099362 | ||||||
chr3:53099510
|
A | G | 109 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(106): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1103-24T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099510 | ||||||
chr3:53099527
|
G | C | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1103-41C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099527 | ||||||
chr3:53099576
|
C | A | 1 | a0001c0001t0002g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1103-90G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099576 | ||||||
chr3:53099653
|
T | C | 1 | a0001c0001t0020g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1103-167A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099653 | ||||||
chr3:53099672
|
T | C | 3 | a0001c0001t0005g0028a0001c0001t0012g0169a0001c0001t0014g0214 | 4 | HG02809.hp1 HG03486.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-186A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099672 | ||||||
chr3:53099760
|
A | G | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1103-274T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099760 | ||||||
chr3:53099816
|
C | T | 1 | a0001c0002t0001g0211 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1103-330G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099816 | ||||||
chr3:53099955
|
T | C | 1 | a0001c0001t0014g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1103-469A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099955 | ||||||
chr3:53100063
|
G | A | 2 | a0001c0002t0001g0218a0001c0002t0001g0219 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1103-577C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100063 | ||||||
chr3:53100082
|
T | C | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1103-596A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100082 | ||||||
chr3:53100184
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1103-698G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100184 | ||||||
chr3:53100294
|
A | C | 1 | a0001c0001t0003g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1103-808T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100294 | ||||||
chr3:53100353
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0087 | 3 | HG00597.hp2 HG02132.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1103-867G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100353 | ||||||
chr3:53100440
|
C | G | 1 | a0001c0001t0003g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1103-954G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100440 | ||||||
chr3:53100682
|
G | A | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.1103-1196C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100682 | ||||||
chr3:53100847
|
T | C | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1103-1361A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100847 | ||||||
chr3:53100955
|
A | G | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1103-1469T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100955 | ||||||
chr3:53100969
|
C | CA | 90 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(87): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1103-1484dupT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100969 | ||||||
chr3:53101150
|
C | T | 1 | a0001c0001t0004g0024 | 2 | HG02738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1103-1664G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101150 | ||||||
chr3:53101439
|
C | G | 1 | a0001c0002t0001g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1103-1953G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101439 | ||||||
chr3:53101623
|
C | T | 1 | a0001c0002t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1103-2137G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101623 | ||||||
chr3:53101682
|
C | T | 1 | a0001c0002t0001g0136 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1103-2196G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101682 | ||||||
chr3:53101922
|
T | C | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1102+2031A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101922 | ||||||
chr3:53101925
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1102+2028C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101925 | ||||||
chr3:53102000
|
G | C | 1 | a0001c0002t0001g0246 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1102+1953C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102000 | ||||||
chr3:53102014
|
G | A | 3 | a0001c0001t0005g0023a0001c0001t0005g0134a0001c0001t0005g0135 | 4 | HG01243.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102+1939C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102014 | ||||||
chr3:53102108
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1102+1845C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102108 | ||||||
chr3:53102414
|
G | A | 1 | a0001c0002t0001g0145 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1102+1539C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102414 | ||||||
chr3:53102445
|
G | A | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1102+1508C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102445 | ||||||
chr3:53102535
|
G | A | 52 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(49): Show | 68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1102+1418C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102535 | ||||||
chr3:53102538
|
A | G | 1 | a0001c0001t0020g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1102+1415T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102538 | ||||||
chr3:53102606
|
C | T | 14 | a0001c0001t0006g0155a0001c0001t0006g0233a0001c0001t0006g0234others(11): Show | 15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1102+1347G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102606 | ||||||
chr3:53102687
|
T | G | 1 | a0001c0001t0003g0072 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1102+1266A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102687 | ||||||
chr3:53102792
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1102+1161C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102792 | ||||||
chr3:53102917
|
G | A | 2 | a0001c0001t0005g0086a0001c0001t0005g0161 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1102+1036C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102917 | ||||||
chr3:53102941
|
C | T | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(1): Show | 4 | HG02572.hp2 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102+1012G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102941 | ||||||
chr3:53103295
|
C | G | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1102+658G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103295 | ||||||
chr3:53103354
|
A | G | 251 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(248): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1102+599T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103354 | ||||||
chr3:53103798
|
T | C | 1 | a0001c0002t0001g0027 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1102+155A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103798 | ||||||
chr3:53103949
|
G | A | 2 | a0001c0001t0005g0086a0001c0001t0005g0161 | 2 | HG02622.hp2 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.1102+4C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103949 | ||||||
chr3:53104211
|
G | A | 14 | a0001c0001t0006g0155a0001c0001t0006g0233a0001c0001t0006g0234others(11): Show | 15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.958-114C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104211 | ||||||
chr3:53104238
|
T | C | 179 | a0001c0001t0002g0190a0001c0001t0003g0002a0001c0001t0003g0007others(176): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.958-141A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104238 | ||||||
chr3:53104279
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.958-182C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104279 | ||||||
chr3:53104329
|
G | T | 1 | a0001c0002t0001g0193 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.958-232C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104329 | ||||||
chr3:53104386
|
C | CT | 11 | a0001c0001t0002g0148a0001c0002t0001g0037a0001c0002t0001g0242others(8): Show | 12 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.958-290dupA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104386 | ||||||
chr3:53105042
|
C | T | 251 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(248): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.957+631G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105042 | ||||||
chr3:53105093
|
T | C | 1 | a0001c0001t0007g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.957+580A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105093 | ||||||
chr3:53105200
|
A | G | 251 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(248): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.957+473T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105200 | ||||||
chr3:53105319
|
C | T | 2 | a0001c0001t0004g0094a0001c0001t0004g0096 | 2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.957+354G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105319 | ||||||
chr3:53105362
|
C | A | 1 | a0001c0001t0014g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957+311G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105362 | ||||||
chr3:53105364
|
A | G | 1 | a0001c0001t0014g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957+309T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105364 | ||||||
chr3:53105410
|
TCCCCG | T | 108 | a0001c0001t0002g0190a0001c0001t0003g0039a0001c0001t0003g0046others(105): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.957+258_957+262del others(5): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105410 | ||||||
chr3:53105411
|
CCCCG | C | 49 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.957+258_957+261del others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105411 | ||||||
chr3:53105412
|
CCCG | C | 18 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0059others(15): Show | 19 | HG01175.hp1 HG02486.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.957+258_957+260del others(3): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105412 | ||||||
chr3:53105415
|
G | C | 2 | a0001c0001t0005g0086a0001c0001t0005g0161 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.957+258C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105415 | ||||||
chr3:53105415
|
G | GC | 16 | a0001c0001t0002g0011a0001c0001t0002g0029a0001c0001t0002g0031others(13): Show | 21 | HG00544.hp1 HG00621.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.957+257dupG | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105415 | ||||||
chr3:53105415
|
GC | G | 18 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(15): Show | 20 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.957+257delG | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105415 | ||||||
chr3:53105417
|
C | G | 3 | a0001c0001t0002g0153a0001c0001t0002g0157a0001c0001t0002g0250 | 3 | HG03098.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.957+256G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105417 | ||||||
chr3:53105417
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.957+256G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105417 | ||||||
chr3:53105424
|
C | A | 1 | a0001c0001t0007g0088 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.957+249G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105424 | ||||||
chr3:53105424
|
C | G | 1 | a0001c0001t0014g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957+249G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105424 | ||||||
chr3:53105425
|
C | G | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.957+248G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105425 | ||||||
chr3:53105426
|
C | A | 4 | a0001c0001t0003g0015a0001c0001t0003g0058a0001c0001t0003g0074others(1): Show | 5 | HG00323.hp2 HG00438.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+247G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105426 | ||||||
chr3:53105490
|
C | T | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.957+183G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105490 | ||||||
chr3:53105491
|
A | G | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.957+182T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105491 | ||||||
chr3:53105628
|
T | C | 5 | a0001c0002t0001g0019a0001c0002t0001g0173a0001c0002t0001g0188others(2): Show | 6 | HG00642.hp2 HG01099.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+45A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105628 | ||||||
chr3:53105961
|
G | A | 110 | a0001c0001t0002g0190a0001c0001t0003g0192a0001c0001t0004g0024others(107): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.827-158C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53105961 | ||||||
chr3:53105997
|
C | A | 1 | a0001c0001t0002g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.827-194G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53105997 | ||||||
chr3:53106187
|
G | A | 13 | a0001c0001t0002g0010a0001c0001t0002g0149a0001c0001t0002g0158others(10): Show | 15 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.827-384C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106187 | ||||||
chr3:53106224
|
C | A | 2 | a0001c0001t0003g0059a0001c0001t0003g0075 | 2 | NA19064.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.827-421G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106224 | ||||||
chr3:53106277
|
T | C | 1 | a0001c0002t0001g0205 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.827-474A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106277 | ||||||
chr3:53106294
|
T | C | 6 | a0001c0001t0005g0028a0001c0001t0009g0151a0001c0001t0009g0258others(3): Show | 7 | HG02647.hp2 HG02809.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-491A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106294 | ||||||
chr3:53106315
|
A | G | 1 | a0002c0003t0006g0223 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.826+504T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106315 | ||||||
chr3:53106319
|
T | G | 15 | a0001c0001t0006g0155a0001c0001t0006g0233a0001c0001t0008g0239others(12): Show | 16 | HG02486.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.826+500A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106319 | ||||||
chr3:53106391
|
AACAGTAC others(8): Show |
A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.826+413_826+427del others(15): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106391 | ||||||
chr3:53106456
|
T | C | 1 | a0001c0001t0003g0076 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.826+363A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106456 | ||||||
chr3:53106529
|
T | C | 1 | a0001c0002t0001g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.826+290A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106529 | ||||||
chr3:53106546
|
G | A | 3 | a0001c0002t0001g0034a0001c0002t0001g0145a0001c0002t0001g0206 | 4 | HG03491.hp1 HG03669.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+273C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106546 | ||||||
chr3:53106587
|
T | C | 169 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(166): Show | 217 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.826+232A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106587 | ||||||
chr3:53106604
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.826+215T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106604 | ||||||
chr3:53106614
|
A | C | 100 | a0001c0001t0002g0029a0001c0001t0002g0045a0001c0001t0002g0148others(97): Show | 124 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.826+205T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106614 | ||||||
chr3:53106747
|
A | C | 1 | a0001c0001t0003g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.826+72T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106747 | ||||||
chr3:53106812
|
A | G | 1 | a0001c0001t0014g0214 | 1 | HG03704.hp1 | splice_region_variant&intron_variant | LOW | c.826+7T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106812 | ||||||
chr3:53107093
|
A | C | 2 | a0001c0002t0001g0252a0001c0002t0001g0253 | 2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.776-224T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107093 | ||||||
chr3:53107136
|
G | GT | 50 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0014others(47): Show | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.776-268dupA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107136 | ||||||
chr3:53107136
|
G | GTT | 13 | a0001c0001t0002g0045a0001c0001t0003g0007a0001c0001t0003g0043others(10): Show | 15 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.776-269_776-268dup others(2): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107136 | ||||||
chr3:53107136
|
GTTTT | G | 167 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(164): Show | 213 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.776-271_776-268del others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107136 | ||||||
chr3:53107177
|
C | T | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-308G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107177 | ||||||
chr3:53107204
|
C | T | 3 | a0001c0002t0001g0021a0001c0002t0001g0121a0001c0002t0001g0126 | 4 | HG01243.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-335G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107204 | ||||||
chr3:53107235
|
A | G | 1 | a0001c0002t0001g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.776-366T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107235 | ||||||
chr3:53107236
|
T | C | 1 | a0002c0003t0005g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.776-367A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107236 | ||||||
chr3:53107290
|
C | T | 20 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(17): Show | 30 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.776-421G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107290 | ||||||
chr3:53107291
|
G | A | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.776-422C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107291 | ||||||
chr3:53107359
|
G | A | 1 | a0001c0001t0002g0032 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.776-490C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107359 | ||||||
chr3:53107491
|
G | A | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.776-622C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107491 | ||||||
chr3:53107500
|
C | G | 54 | a0001c0001t0002g0045a0001c0001t0003g0002a0001c0001t0003g0007others(51): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.776-631G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107500 | ||||||
chr3:53107533
|
C | T | 54 | a0001c0001t0002g0045a0001c0001t0003g0002a0001c0001t0003g0007others(51): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.776-664G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107533 | ||||||
chr3:53107708
|
A | G | 1 | a0001c0001t0007g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.776-839T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107708 | ||||||
chr3:53107821
|
G | C | 13 | a0001c0001t0006g0233a0001c0001t0006g0234a0002c0003t0006g0035others(10): Show | 14 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.776-952C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107821 | ||||||
chr3:53107850
|
A | C | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.776-981T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107850 | ||||||
chr3:53107896
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.776-1027G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107896 | ||||||
chr3:53107911
|
C | T | 1 | a0001c0001t0005g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.776-1042G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107911 | ||||||
chr3:53107913
|
C | G | 1 | a0001c0002t0001g0132 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.776-1044G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107913 | ||||||
chr3:53107949
|
G | C | 53 | a0001c0001t0002g0045a0001c0001t0003g0002a0001c0001t0003g0007others(50): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.776-1080C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107949 | ||||||
chr3:53108055
|
G | A | 20 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(17): Show | 30 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.776-1186C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108055 | ||||||
chr3:53108058
|
T | G | 1 | a0001c0001t0003g0078 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.776-1189A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108058 | ||||||
chr3:53108071
|
CAG | C | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG02040.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.776-1204_776-1203d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108071 | ||||||
chr3:53108072
|
A | T | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.776-1203T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108072 | ||||||
chr3:53108080
|
A | T | 1 | a0001c0002t0001g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.776-1211T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108080 | ||||||
chr3:53108205
|
A | T | 53 | a0001c0001t0002g0045a0001c0001t0003g0002a0001c0001t0003g0007others(50): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.776-1336T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108205 | ||||||
chr3:53108240
|
A | G | 53 | a0001c0001t0002g0045a0001c0001t0003g0002a0001c0001t0003g0007others(50): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.776-1371T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108240 | ||||||
chr3:53108341
|
T | G | 2 | a0001c0001t0002g0149a0001c0001t0006g0155 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.776-1472A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108341 | ||||||
chr3:53108357
|
C | T | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.776-1488G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108357 | ||||||
chr3:53108389
|
CT | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(154): Show | 202 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.776-1521delA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108389 | ||||||
chr3:53108389
|
CTT | C | 19 | a0001c0001t0005g0086a0001c0001t0006g0233a0001c0001t0006g0234others(16): Show | 21 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.776-1522_776-1521d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108389 | ||||||
chr3:53108585
|
G | C | 1 | a0002c0003t0006g0225 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.776-1716C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108585 | ||||||
chr3:53108693
|
T | A | 2 | a0001c0001t0002g0049a0001c0001t0016g0048 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.776-1824A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108693 | ||||||
chr3:53108703
|
G | GT | 35 | a0001c0001t0002g0176a0001c0001t0002g0183a0001c0001t0002g0190others(32): Show | 39 | HG00621.hp1 HG01109.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.776-1835dupA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108703 | ||||||
chr3:53108825
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.776-1956G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108825 | ||||||
chr3:53108946
|
G | C | 1 | a0001c0001t0007g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.776-2077C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108946 | ||||||
chr3:53108964
|
G | A | 68 | a0001c0001t0004g0024a0001c0001t0005g0023a0001c0001t0005g0134others(65): Show | 91 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.776-2095C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108964 | ||||||
chr3:53109143
|
A | T | 1 | a0001c0002t0001g0108 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.776-2274T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109143 | ||||||
chr3:53109362
|
A | G | 20 | a0001c0001t0005g0086a0001c0001t0006g0233a0001c0001t0006g0234others(17): Show | 22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.775+2468T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109362 | ||||||
chr3:53109459
|
T | C | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.775+2371A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109459 | ||||||
chr3:53109568
|
G | C | 20 | a0001c0001t0005g0086a0001c0001t0006g0233a0001c0001t0006g0234others(17): Show | 22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.775+2262C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109568 | ||||||
chr3:53109710
|
G | A | 1 | a0001c0002t0024g0186 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.775+2120C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109710 | ||||||
chr3:53109760
|
G | A | 20 | a0001c0001t0005g0086a0001c0001t0006g0233a0001c0001t0006g0234others(17): Show | 22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.775+2070C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109760 | ||||||
chr3:53109844
|
A | C | 2 | a0001c0001t0008g0012a0001c0001t0008g0237 | 4 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+1986T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109844 | ||||||
chr3:53109885
|
A | G | 54 | a0001c0001t0002g0045a0001c0001t0003g0002a0001c0001t0003g0007others(51): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.775+1945T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109885 | ||||||
chr3:53110032
|
A | G | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775+1798T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110032 | ||||||
chr3:53110071
|
T | C | 1 | a0001c0002t0001g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.775+1759A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110071 | ||||||
chr3:53110224
|
C | T | 1 | a0001c0002t0001g0129 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.775+1606G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110224 | ||||||
chr3:53110347
|
T | C | 54 | a0001c0001t0002g0045a0001c0001t0003g0002a0001c0001t0003g0007others(51): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.775+1483A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110347 | ||||||
chr3:53110386
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.775+1444G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110386 | ||||||
chr3:53110518
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.775+1312C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110518 | ||||||
chr3:53110913
|
T | C | 1 | a0008c0006t0006g0232 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.775+917A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110913 | ||||||
chr3:53110934
|
C | T | 1 | a0001c0002t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.775+896G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110934 | ||||||
chr3:53111181
|
G | A | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+649C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53111181 | ||||||
chr3:53111226
|
A | G | 1 | a0001c0002t0001g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.775+604T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53111226 | ||||||
chr3:53112177
|
C | T | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.697-269G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112177 | ||||||
chr3:53112542
|
G | A | 1 | a0001c0001t0005g0161 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.697-634C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112542 | ||||||
chr3:53112716
|
C | A | 19 | a0001c0001t0002g0010a0001c0001t0002g0148a0001c0001t0002g0149others(16): Show | 21 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.697-808G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112716 | ||||||
chr3:53112866
|
C | G | 1 | a0008c0006t0006g0232 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.697-958G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112866 | ||||||
chr3:53113222
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-1314C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113222 | ||||||
chr3:53113222
|
G | T | 1 | a0001c0001t0003g0047 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.697-1314C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113222 | ||||||
chr3:53113237
|
A | T | 1 | a0001c0002t0001g0188 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.697-1329T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113237 | ||||||
chr3:53113246
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1338C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113246 | ||||||
chr3:53113251
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1343T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113251 | ||||||
chr3:53113254
|
A | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1346T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113254 | ||||||
chr3:53113257
|
C | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1349G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113257 | ||||||
chr3:53113258
|
C | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1350G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113258 | ||||||
chr3:53113260
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1352G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113260 | ||||||
chr3:53113267
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1359G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113267 | ||||||
chr3:53113268
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1360C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113268 | ||||||
chr3:53113269
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1361C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113269 | ||||||
chr3:53113270
|
C | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1362G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113270 | ||||||
chr3:53113272
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1364G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113272 | ||||||
chr3:53113276
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1368T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113276 | ||||||
chr3:53113277
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1369T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113277 | ||||||
chr3:53113278
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1370C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113278 | ||||||
chr3:53113279
|
T | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1371A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113279 | ||||||
chr3:53113281
|
C | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1373G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113281 | ||||||
chr3:53113282
|
T | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1374A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113282 | ||||||
chr3:53113283
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1375C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113283 | ||||||
chr3:53113284
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1376C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113284 | ||||||
chr3:53113292
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1384C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113292 | ||||||
chr3:53113293
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1385C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113293 | ||||||
chr3:53113311
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1403C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113311 | ||||||
chr3:53113313
|
T | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1405A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113313 | ||||||
chr3:53113321
|
A | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1413T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113321 | ||||||
chr3:53113322
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1414C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113322 | ||||||
chr3:53113323
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1415C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113323 | ||||||
chr3:53113329
|
A | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1421T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113329 | ||||||
chr3:53113332
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1424G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113332 | ||||||
chr3:53113334
|
T | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1426A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113334 | ||||||
chr3:53113336
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1428C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113336 | ||||||
chr3:53113338
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1430C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113338 | ||||||
chr3:53113339
|
T | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1431A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113339 | ||||||
chr3:53113340
|
A | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1432T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113340 | ||||||
chr3:53113341
|
C | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1433G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113341 | ||||||
chr3:53113344
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1436C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113344 | ||||||
chr3:53113352
|
A | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1444T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113352 | ||||||
chr3:53113356
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1448C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113356 | ||||||
chr3:53113357
|
T | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1449A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113357 | ||||||
chr3:53113358
|
A | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1450T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113358 | ||||||
chr3:53113361
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1453C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113361 | ||||||
chr3:53113364
|
T | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1456A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113364 | ||||||
chr3:53113367
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1459G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113367 | ||||||
chr3:53113369
|
A | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1461T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113369 | ||||||
chr3:53113371
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1463T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113371 | ||||||
chr3:53113372
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1464C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113372 | ||||||
chr3:53113374
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1466C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113374 | ||||||
chr3:53113378
|
A | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1470T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113378 | ||||||
chr3:53113380
|
T | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1472A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113380 | ||||||
chr3:53113384
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1476G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113384 | ||||||
chr3:53113385
|
A | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1477T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113385 | ||||||
chr3:53113389
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1481C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113389 | ||||||
chr3:53113390
|
TAGGATTT others(3): Show |
T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.697-1492_697-1483d others(12): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113390 | ||||||
chr3:53113397
|
T | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1489A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113397 | ||||||
chr3:53113402
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1494C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113402 | ||||||
chr3:53113403
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1495C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113403 | ||||||
chr3:53113404
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1496C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113404 | ||||||
chr3:53113406
|
T | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1498A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113406 | ||||||
chr3:53113413
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1505C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113413 | ||||||
chr3:53113414
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1506T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113414 | ||||||
chr3:53113416
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1508C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113416 | ||||||
chr3:53113417
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1509C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113417 | ||||||
chr3:53113420
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1512C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113420 | ||||||
chr3:53113421
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1513C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113421 | ||||||
chr3:53113422
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1514C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113422 | ||||||
chr3:53113430
|
A | C | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1522T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113430 | ||||||
chr3:53113433
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1525T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113433 | ||||||
chr3:53113434
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1526T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113434 | ||||||
chr3:53113435
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1527C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113435 | ||||||
chr3:53113437
|
C | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1529G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113437 | ||||||
chr3:53113438
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1530G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113438 | ||||||
chr3:53113439
|
A | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1531T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113439 | ||||||
chr3:53113441
|
G | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1533C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113441 | ||||||
chr3:53113442
|
C | G | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1534G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113442 | ||||||
chr3:53113443
|
C | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1535G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113443 | ||||||
chr3:53113445
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1537T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113445 | ||||||
chr3:53113448
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1540G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113448 | ||||||
chr3:53113450
|
A | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1542T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113450 | ||||||
chr3:53113452
|
C | A | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1544G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113452 | ||||||
chr3:53113454
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1546G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113454 | ||||||
chr3:53113463
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.697-1555C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113463 | ||||||
chr3:53113560
|
C | A | 19 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(16): Show | 29 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.697-1652G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113560 | ||||||
chr3:53113635
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.697-1727A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113635 | ||||||
chr3:53113796
|
A | C | 1 | a0001c0001t0002g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.697-1888T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113796 | ||||||
chr3:53113808
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-1900A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113808 | ||||||
chr3:53113870
|
C | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.697-1962G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113870 | ||||||
chr3:53113923
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.697-2015G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113923 | ||||||
chr3:53114014
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.697-2106A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114014 | ||||||
chr3:53114105
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.697-2197G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114105 | ||||||
chr3:53114126
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-2218C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114126 | ||||||
chr3:53114158
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.697-2250C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114158 | ||||||
chr3:53114292
|
G | A | 3 | a0001c0002t0001g0170a0001c0002t0001g0218a0001c0002t0001g0219 | 3 | HG00639.hp1 HG01069.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.697-2384C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114292 | ||||||
chr3:53114302
|
T | C | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.697-2394A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114302 | ||||||
chr3:53114439
|
G | C | 165 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(162): Show | 211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.697-2531C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114439 | ||||||
chr3:53114573
|
G | A | 7 | a0001c0001t0003g0081a0002c0003t0005g0036a0002c0003t0005g0089others(4): Show | 8 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.697-2665C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114573 | ||||||
chr3:53114579
|
T | C | 13 | a0001c0001t0006g0233a0001c0001t0006g0234a0002c0003t0006g0035others(10): Show | 14 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.697-2671A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114579 | ||||||
chr3:53114732
|
GC | G | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.697-2825delG | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114732 | ||||||
chr3:53114794
|
C | A | 6 | a0002c0003t0005g0036a0002c0003t0005g0089a0002c0003t0005g0228others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.697-2886G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114794 | ||||||
chr3:53114817
|
T | A | 1 | a0001c0001t0002g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.697-2909A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114817 | ||||||
chr3:53114817
|
T | G | 220 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(217): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.697-2909A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114817 | ||||||
chr3:53114942
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.697-3034T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114942 | ||||||
chr3:53114952
|
C | T | 1 | a0001c0001t0002g0011 | 3 | HG01070.hp1 HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.697-3044G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114952 | ||||||
chr3:53115099
|
A | G | 1 | a0001c0002t0001g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.697-3191T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115099 | ||||||
chr3:53115205
|
T | C | 4 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0102others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-3297A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115205 | ||||||
chr3:53115248
|
C | G | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.697-3340G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115248 | ||||||
chr3:53115248
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.697-3340G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115248 | ||||||
chr3:53115252
|
G | A | 20 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(17): Show | 22 | HG00673.hp1 HG01346.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.697-3344C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115252 | ||||||
chr3:53115614
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.697-3706A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115614 | ||||||
chr3:53116101
|
G | A | 4 | a0001c0002t0001g0185a0001c0002t0001g0209a0001c0002t0001g0210others(1): Show | 4 | NA18961.hp2 NA18971.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+3783C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116101 | ||||||
chr3:53116291
|
CT | C | 76 | a0001c0001t0002g0045a0001c0001t0002g0190a0001c0001t0003g0046others(73): Show | 87 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.696+3592delA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116291 | ||||||
chr3:53116291
|
CTT | C | 178 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(175): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.696+3591_696+3592d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116291 | ||||||
chr3:53116329
|
T | C | 2 | a0001c0001t0005g0028a0001c0001t0012g0169 | 3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.696+3555A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116329 | ||||||
chr3:53116333
|
G | A | 6 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(3): Show | 7 | HG02258.hp2 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.696+3551C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116333 | ||||||
chr3:53116418
|
A | G | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.696+3466T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116418 | ||||||
chr3:53116578
|
G | A | 1 | a0001c0002t0001g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.696+3306C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116578 | ||||||
chr3:53116984
|
G | T | 19 | a0001c0001t0006g0233a0001c0001t0006g0234a0002c0003t0005g0036others(16): Show | 21 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.696+2900C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116984 | ||||||
chr3:53117330
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.696+2554G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117330 | ||||||
chr3:53117648
|
A | C | 56 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(53): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.696+2236T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117648 | ||||||
chr3:53117703
|
G | A | 2 | a0001c0001t0005g0028a0001c0001t0012g0169 | 3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.696+2181C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117703 | ||||||
chr3:53117754
|
C | T | 1 | a0001c0002t0001g0020 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.696+2130G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117754 | ||||||
chr3:53118042
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.696+1842T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118042 | ||||||
chr3:53118046
|
T | C | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(236): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.696+1838A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118046 | ||||||
chr3:53118066
|
T | A | 256 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(253): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.696+1818A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118066 | ||||||
chr3:53118091
|
C | T | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+1793G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118091 | ||||||
chr3:53118098
|
A | G | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.696+1786T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118098 | ||||||
chr3:53118435
|
G | C | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.696+1449C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118435 | ||||||
chr3:53118587
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.696+1297T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118587 | ||||||
chr3:53118706
|
T | C | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+1178A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118706 | ||||||
chr3:53118755
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.696+1129C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118755 | ||||||
chr3:53118906
|
A | G | 1 | a0001c0001t0003g0043 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.696+978T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118906 | ||||||
chr3:53119047
|
CA | C | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.696+836delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119047 | ||||||
chr3:53119056
|
A | T | 2 | a0001c0001t0004g0091a0001c0001t0004g0092 | 2 | HG00673.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.696+828T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119056 | ||||||
chr3:53119122
|
G | C | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.696+762C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119122 | ||||||
chr3:53119177
|
A | C | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.696+707T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119177 | ||||||
chr3:53119182
|
A | C | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.696+702T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119182 | ||||||
chr3:53119333
|
T | C | 3 | a0001c0001t0008g0012a0001c0001t0008g0237a0001c0001t0008g0239 | 5 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.696+551A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119333 | ||||||
chr3:53119415
|
A | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.696+469T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119415 | ||||||
chr3:53119649
|
C | A | 1 | a0001c0001t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.696+235G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119649 | ||||||
chr3:53120116
|
ATTAACTG others(3): Show |
A | 56 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(53): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.559-105_559-96delG others(9): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120116 | ||||||
chr3:53120127
|
T | G | 56 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(53): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.559-106A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120127 | ||||||
chr3:53120133
|
T | G | 1 | a0001c0001t0005g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.559-112A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120133 | ||||||
chr3:53120251
|
C | G | 6 | a0001c0002t0001g0037a0001c0002t0001g0242a0001c0002t0001g0243others(3): Show | 7 | HG00639.hp2 HG01074.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.559-230G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120251 | ||||||
chr3:53120300
|
C | G | 2 | a0001c0002t0001g0185a0003c0004t0001g0038 | 2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.559-279G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120300 | ||||||
chr3:53120350
|
C | T | 1 | a0001c0002t0001g0184 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.559-329G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120350 | ||||||
chr3:53120445
|
T | C | 2 | a0001c0002t0001g0110a0001c0002t0001g0213 | 2 | NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.559-424A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120445 | ||||||
chr3:53120448
|
A | T | 1 | a0001c0001t0003g0042 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.559-427T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120448 | ||||||
chr3:53120489
|
T | C | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.559-468A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120489 | ||||||
chr3:53120663
|
A | G | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.559-642T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120663 | ||||||
chr3:53120852
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.559-831G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120852 | ||||||
chr3:53120884
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.558+815T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120884 | ||||||
chr3:53120972
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.558+727G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120972 | ||||||
chr3:53121002
|
A | T | 1 | a0001c0001t0008g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.558+697T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121002 | ||||||
chr3:53121056
|
C | T | 19 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(16): Show | 29 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.558+643G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121056 | ||||||
chr3:53121142
|
C | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.558+557G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121142 | ||||||
chr3:53121157
|
G | C | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164 | 3 | HG01934.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.558+542C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121157 | ||||||
chr3:53121259
|
A | T | 257 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(254): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.558+440T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121259 | ||||||
chr3:53121944
|
T | C | 1 | a0001c0001t0014g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.457-144A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53121944 | ||||||
chr3:53122004
|
A | G | 1 | a0001c0001t0020g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.457-204T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53122004 | ||||||
chr3:53122049
|
G | C | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.457-249C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53122049 | ||||||
chr3:53122276
|
T | A | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02922.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.456+98A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53122276 | ||||||
chr3:53122583
|
T | A | 23 | a0001c0001t0002g0010a0001c0001t0002g0148a0001c0001t0002g0149others(20): Show | 25 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.267-20A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53122583 | ||||||
chr3:53122676
|
T | A | 1 | a0001c0002t0001g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.267-113A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53122676 | ||||||
chr3:53122851
|
T | C | 56 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(53): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.267-288A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53122851 | ||||||
chr3:53123040
|
TGGGGCAC others(22): Show |
T | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.267-506_267-478del others(29): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123040 | ||||||
chr3:53123286
|
A | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.266+438T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123286 | ||||||
chr3:53123419
|
C | T | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.266+305G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123419 | ||||||
chr3:53123453
|
C | T | 17 | a0002c0003t0005g0036a0002c0003t0005g0089a0002c0003t0005g0228others(14): Show | 19 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.266+271G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123453 | ||||||
chr3:53123530
|
T | C | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.266+194A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123530 | ||||||
chr3:53123544
|
G | A | 2 | a0001c0002t0001g0218a0001c0002t0001g0219 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.266+180C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123544 | ||||||
chr3:53123587
|
T | C | 6 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(3): Show | 7 | HG02258.hp2 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+137A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123587 | ||||||
chr3:53123888
|
AGAGAACT others(5): Show |
A | 1 | a0001c0002t0001g0006 | 4 | HG00621.hp2 NA18941.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-60_150-49delCC others(10): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53123888 | ||||||
chr3:53123955
|
G | A | 1 | a0007c0007t0004g0103 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.150-115C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53123955 | ||||||
chr3:53124064
|
G | A | 1 | a0001c0002t0021g0168 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.150-224C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124064 | ||||||
chr3:53124142
|
T | C | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(236): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.150-302A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124142 | ||||||
chr3:53124382
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.150-542C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124382 | ||||||
chr3:53124752
|
A | G | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(236): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.150-912T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124752 | ||||||
chr3:53124815
|
T | A | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.150-975A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124815 | ||||||
chr3:53124819
|
A | G | 2 | a0001c0002t0001g0173a0001c0002t0023g0172 | 2 | HG01255.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.150-979T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124819 | ||||||
chr3:53124877
|
C | G | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.149+1032G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124877 | ||||||
chr3:53124878
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.149+1031C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124878 | ||||||
chr3:53124937
|
A | C | 1 | a0001c0002t0001g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.149+972T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124937 | ||||||
chr3:53124970
|
G | A | 1 | a0001c0002t0001g0006 | 4 | HG00621.hp2 NA18941.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+939C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124970 | ||||||
chr3:53124973
|
T | A | 1 | a0001c0002t0001g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.149+936A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124973 | ||||||
chr3:53125208
|
G | C | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.149+701C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125208 | ||||||
chr3:53125302
|
C | G | 1 | a0001c0002t0001g0171 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.149+607G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125302 | ||||||
chr3:53125438
|
C | A | 1 | a0001c0002t0001g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.149+471G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125438 | ||||||
chr3:53125444
|
C | G | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.149+465G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125444 | ||||||
chr3:53125493
|
A | C | 1 | a0001c0002t0001g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.149+416T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125493 | ||||||
chr3:53125494
|
AG | A | 10 | a0001c0002t0001g0037a0001c0002t0001g0242a0001c0002t0001g0243others(7): Show | 11 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.149+414delC | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125494 | ||||||
chr3:53126008
|
G | A | 6 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(3): Show | 7 | HG02258.hp2 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-14C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126008 | ||||||
chr3:53126067
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.64-73A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126067 | ||||||
chr3:53126116
|
T | C | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-122A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126116 | ||||||
chr3:53126177
|
G | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-183C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126177 | ||||||
chr3:53126200
|
T | C | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-206A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126200 | ||||||
chr3:53126227
|
G | A | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-233C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126227 | ||||||
chr3:53126253
|
A | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-259T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126253 | ||||||
chr3:53126254
|
C | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-260G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126254 | ||||||
chr3:53126255
|
C | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-261G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126255 | ||||||
chr3:53126344
|
G | A | 62 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0029others(59): Show | 80 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.64-350C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126344 | ||||||
chr3:53126364
|
C | G | 1 | a0001c0001t0011g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-370G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126364 | ||||||
chr3:53126389
|
T | C | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(236): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.64-395A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126389 | ||||||
chr3:53126446
|
C | CTAATTTC others(321): Show |
1 | a0001c0002t0010g0114 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.64-453_64-452insCT others(326): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126446 | ||||||
chr3:53126446
|
C | CTAATTTC others(322): Show |
1 | a0001c0002t0010g0113 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.64-453_64-452insCT others(327): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126446 | ||||||
chr3:53126905
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-911A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126905 | ||||||
chr3:53127015
|
A | G | 240 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(237): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.64-1021T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127015 | ||||||
chr3:53127092
|
C | T | 1 | a0001c0002t0001g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64-1098G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127092 | ||||||
chr3:53127292
|
T | A | 2 | a0001c0002t0001g0218a0001c0002t0001g0219 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.64-1298A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127292 | ||||||
chr3:53127468
|
G | A | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-1474C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127468 | ||||||
chr3:53127492
|
G | C | 20 | a0001c0001t0002g0240a0001c0001t0006g0233a0001c0001t0006g0234others(17): Show | 22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-1498C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127492 | ||||||
chr3:53127557
|
T | C | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(236): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.64-1563A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127557 | ||||||
chr3:53127619
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.64-1625C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127619 | ||||||
chr3:53127652
|
TA | T | 193 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(190): Show | 242 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.64-1659delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127652 | ||||||
chr3:53127652
|
TAA | T | 6 | a0001c0001t0009g0258a0001c0002t0001g0107a0001c0002t0001g0108others(3): Show | 6 | HG01167.hp2 HG02735.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1660_64-1659del others(2): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127652 | ||||||
chr3:53127884
|
C | G | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.64-1890G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127884 | ||||||
chr3:53127929
|
C | A | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.64-1935G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127929 | ||||||
chr3:53128024
|
G | A | 1 | a0001c0002t0001g0241 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.64-2030C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128024 | ||||||
chr3:53128263
|
A | C | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+2075T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128263 | ||||||
chr3:53128322
|
T | A | 9 | a0001c0002t0001g0037a0001c0002t0001g0242a0001c0002t0001g0243others(6): Show | 10 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+2016A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128322 | ||||||
chr3:53128390
|
G | A | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+1948C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128390 | ||||||
chr3:53128429
|
A | G | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+1909T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128429 | ||||||
chr3:53128443
|
C | T | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+1895G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128443 | ||||||
chr3:53128444
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+1894C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128444 | ||||||
chr3:53128644
|
G | C | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+1694C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128644 | ||||||
chr3:53128656
|
G | T | 17 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0085others(14): Show | 19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+1682C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128656 | ||||||
chr3:53128731
|
C | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+1607G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128731 | ||||||
chr3:53128802
|
C | T | 1 | a0002c0003t0005g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.63+1536G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128802 | ||||||
chr3:53128942
|
G | C | 1 | a0001c0002t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+1396C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128942 | ||||||
chr3:53129041
|
A | T | 55 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(52): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+1297T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129041 | ||||||
chr3:53129200
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.63+1138T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129200 | ||||||
chr3:53129308
|
G | T | 1 | a0001c0001t0005g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+1030C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129308 | ||||||
chr3:53129359
|
C | T | 1 | a0001c0001t0004g0085 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.63+979G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129359 | ||||||
chr3:53129671
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+667C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129671 | ||||||
chr3:53129676
|
G | A | 2 | a0001c0002t0001g0252a0001c0002t0001g0253 | 2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.63+662C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129676 | ||||||
chr3:53129685
|
T | C | 1 | a0001c0001t0020g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+653A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129685 | ||||||
chr3:53129814
|
G | A | 1 | a0001c0002t0001g0255 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.63+524C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129814 | ||||||
chr3:53129873
|
T | C | 1 | a0001c0002t0001g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.63+465A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129873 | ||||||
chr3:53129922
|
A | T | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+416T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129922 | ||||||
chr3:53129926
|
A | T | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+412T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129926 | ||||||
chr3:53129927
|
T | A | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+411A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129927 | ||||||
chr3:53129931
|
A | T | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+407T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129931 | ||||||
chr3:53129933
|
A | T | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+405T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129933 | ||||||
chr3:53129934
|
T | TCTTTTCT others(9): Show |
1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+403_63+404insGA others(14): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129934 | ||||||
chr3:53129937
|
A | T | 54 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(51): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+401T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129937 | ||||||
chr3:53129939
|
T | TTAGCACT others(4): Show |
1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+398_63+399insCA others(9): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129939 | ||||||
chr3:53129940
|
C | T | 1 | a0005c0009t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+398G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129940 | ||||||
chr3:53130078
|
C | T | 54 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(51): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+260G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130078 | ||||||
chr3:53130177
|
C | T | 54 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0003g0002others(51): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+161G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130177 | ||||||
chr3:53130200
|
T | C | 1 | a0001c0001t0003g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.63+138A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130200 | ||||||
chr3:53130222
|
T | G | 1 | a0001c0001t0009g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+116A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130222 |