geneid | 9617 |
---|---|
ensemblid | ENSG00000120662.16 |
hgncid | 7469 |
symbol | MTRF1 |
name | mitochondrial translation release factor 1 |
refseq_nuc | NM_004294.4 |
refseq_prot | NP_004285.2 |
ensembl_nuc | ENST00000379480.9 |
ensembl_prot | ENSP00000368793.3 |
mane_status | MANE Select |
chr | chr13 |
start | 41216369 |
end | 41263576 |
strand | - |
ver | v1.2 |
region | chr13:41216369-41263576 |
region5000 | chr13:41211369-41268576 |
regionname0 | MTRF1_chr13_41216369_41263576 |
regionname5000 | MTRF1_chr13_41211369_41268576 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 445 | 309 | 71 | 46 | 157 | 9 | 24 | 125 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0002 | 0/0 | 445 | 10 | 5 | 4 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0003 | 0/0 | 445 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0004 | 0/0 | 445 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0005 | 0/0 | 445 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0006 | 0/0 | 445 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0007 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1338 | 175 | 45 | 29 | 85 | 5 | 10 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0002 | 1/0 | 1338 | 130 | 23 | 16 | 72 | 4 | 14 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0003 | 0/0 | 1338 | 8 | 5 | 2 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0004 | 0/0 | 1338 | 5 | 5 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0005 | 0/0 | 1338 | 4 | 2 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0006 | 0/0 | 1338 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0007 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0008 | 0/0 | 1338 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0009 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0010 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
c0011 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 847 | 293 | 70 | 51 | 137 | 9 | 24 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
t0002 | 0/0 | 847 | 21 | 0 | 0 | 21 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
t0003 | 0/0 | 847 | 10 | 10 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
t0004 | 0/0 | 847 | 6 | 4 | 1 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
t0005 | 0/0 | 847 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
t0006 | 0/0 | 847 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0003 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0011 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1338 | 175 | 45 | 29 | 85 | 5 | 10 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0002 | 1/0 | 1338 | 130 | 23 | 16 | 72 | 4 | 14 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0006 | 0/0 | 1338 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0010 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0002c0003 | 0/0 | 1338 | 8 | 5 | 2 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0002c0008 | 0/0 | 1338 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0003c0004 | 0/0 | 1338 | 5 | 5 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0004c0005 | 0/0 | 1338 | 4 | 2 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0005c0007 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0006c0009 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0007c0011 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2184 | 152 | 37 | 29 | 70 | 5 | 10 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0001t0002 | 0/0 | 2184 | 15 | 0 | 0 | 15 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0001t0003 | 0/0 | 2184 | 6 | 6 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0001t0005 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0001t0006 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0002t0001 | 1/0 | 2184 | 124 | 23 | 16 | 66 | 4 | 14 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0002t0002 | 0/0 | 2184 | 6 | 0 | 0 | 6 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0006t0003 | 0/0 | 2184 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0001c0010t0001 | 0/0 | 2184 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0002c0003t0001 | 0/0 | 2184 | 2 | 1 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0002c0003t0004 | 0/0 | 2184 | 6 | 4 | 1 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0002c0008t0001 | 0/0 | 2184 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0003c0004t0001 | 0/0 | 2184 | 5 | 5 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0004c0005t0001 | 0/0 | 2184 | 4 | 2 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0005c0007t0001 | 0/0 | 2184 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0006c0009t0001 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
a0007c0011t0003 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | copy fasta | chr13 | 41211369 | 41268576 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0003 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0011 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0006t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0006t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0006t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0001c0010t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0003t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0008t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0002c0008t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0003c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0003c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0003c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0003c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0003c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0004c0005t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0004c0005t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0004c0005t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0004c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0005c0007t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0005c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0006c0009t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
a0007c0011t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | GBR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00280 | hp2 | a0002 | c0003 | t0004 | g0172 | EUR | FIN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01069 | hp1 | a0002 | c0008 | t0001 | g0278 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01071 | hp1 | a0002 | c0008 | t0001 | g0277 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01109 | hp1 | a0004 | c0005 | t0001 | g0183 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01169 | hp2 | a0001 | c0010 | t0001 | g0113 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01192 | hp1 | a0004 | c0005 | t0001 | g0184 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01192 | hp2 | a0002 | c0003 | t0004 | g0174 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0024 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0227 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01891 | hp1 | a0003 | c0004 | t0001 | g0177 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01981 | hp1 | a0002 | c0003 | t0001 | g0182 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02055 | hp1 | a0002 | c0003 | t0004 | g0173 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02615 | hp1 | a0002 | c0003 | t0004 | g0176 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02622 | hp2 | a0005 | c0007 | t0001 | g0046 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0087 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02630 | hp2 | a0001 | c0006 | t0003 | g0036 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02717 | hp1 | a0005 | c0007 | t0001 | g0045 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02818 | hp1 | a0003 | c0004 | t0001 | g0180 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02818 | hp2 | a0007 | c0011 | t0003 | g0169 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0181 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02895 | hp2 | a0004 | c0005 | t0001 | g0185 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02897 | hp1 | a0004 | c0005 | t0001 | g0186 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02976 | hp1 | a0003 | c0004 | t0001 | g0179 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03453 | hp1 | a0003 | c0004 | t0001 | g0175 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03516 | hp1 | a0001 | c0006 | t0003 | g0038 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0246 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0230 | SAS | BEB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18522 | hp2 | a0003 | c0004 | t0001 | g0178 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | CHB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18953 | hp2 | a0006 | c0009 | t0001 | g0072 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19072 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | TSI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02486 | hp1 | a0002 | c0003 | t0004 | g0170 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG02559 | hp2 | a0001 | c0006 | t0003 | g0039 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA20300 | hp2 | a0002 | c0003 | t0004 | g0171 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0242 | REF | REF | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41217138
|
C | T | 1 | a0007 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1315G>A | p.Glu439Lys | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 1415/2184 | 1315/1338 | 439/445 | chr13 | 41217138 | ||
chr13:41217174
|
A | C | 1 | a0003 | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.1279T>G | p.Ser427Ala | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 1379/2184 | 1279/1338 | 427/445 | chr13 | 41217174 | ||
chr13:41223261
|
T | C | 2 | a0004a0005 | 6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
missense_variant | MODERATE | c.1219A>G | p.Ile407Val | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/10 | 1319/2184 | 1219/1338 | 407/445 | chr13 | 41223261 | ||
chr13:41223350
|
C | G | 1 | a0006 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.1130G>C | p.Gly377Ala | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/10 | 1230/2184 | 1130/1338 | 377/445 | chr13 | 41223350 | ||
chr13:41260903
|
T | C | 4 | a0002a0003a0004others(1): Show | 20 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
missense_variant | MODERATE | c.5A>G | p.Asn2Ser | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/10 | 105/2184 | 5/1338 | 2/445 | chr13 | 41260903 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41240402
|
G | A | 1 | a0001c0010 | 1 | HG01169.hp2 | synonymous_variant | LOW | c.729C>T | p.Ser243Ser | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/10 | 829/2184 | 729/1338 | 243/445 | chr13 | 41240402 | ||
chr13:41252679
|
T | C | 1 | a0001c0006 | 3 | HG02559.hp2 HG02630.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.663A>G | p.Gln221Gln | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/10 | 763/2184 | 663/1338 | 221/445 | chr13 | 41252679 | ||
chr13:41252956
|
A | T | 1 | a0002c0008 | 2 | HG01069.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.582T>A | p.Thr194Thr | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 4/10 | 682/2184 | 582/1338 | 194/445 | chr13 | 41252956 | ||
chr13:41260608
|
C | T | 10 | a0001c0001a0001c0006a0001c0010others(7): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
synonymous_variant | LOW | c.300G>A | p.Glu100Glu | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/10 | 400/2184 | 300/1338 | 100/445 | chr13 | 41260608 | ||
chr13:41260620
|
G | A | 1 | a0004c0005 | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
synonymous_variant | LOW | c.288C>T | p.Ile96Ile | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/10 | 388/2184 | 288/1338 | 96/445 | chr13 | 41260620 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41216448
|
A | C | 1 | a0002c0003t0004 | 6 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*667T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 667 | chr13 | 41216448 | |||||
chr13:41216596
|
C | A | 2 | a0001c0001t0002a0001c0002t0002 | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*519G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 519 | chr13 | 41216596 | |||||
chr13:41216891
|
T | G | 1 | a0001c0001t0006 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 224 | chr13 | 41216891 | |||||
chr13:41216980
|
C | T | 1 | a0001c0001t0005 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 135 | chr13 | 41216980 | |||||
chr13:41217112
|
T | C | 3 | a0001c0001t0003a0001c0006t0003a0007c0011t0003 | 10 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 3 | chr13 | 41217112 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41217304
|
T | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(114): Show | 137 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1225-76A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217304 | ||||||
chr13:41217434
|
T | A | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1225-206A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217434 | ||||||
chr13:41217484
|
A | G | 9 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-256T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217484 | ||||||
chr13:41217619
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1225-391G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217619 | ||||||
chr13:41217621
|
TA | T | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-394delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217621 | ||||||
chr13:41218021
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1225-793A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218021 | ||||||
chr13:41218121
|
A | C | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1225-893T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218121 | ||||||
chr13:41218280
|
AATTTTTT others(11): Show |
A | 5 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG00280.hp1 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1070_1225-105 others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218280 | ||||||
chr13:41218281
|
A | AT | 31 | a0001c0001t0001g0052a0001c0001t0003g0031a0001c0002t0001g0006others(28): Show | 35 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1225-1054dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218281
|
AT | A | 8 | a0001c0001t0002g0048a0001c0001t0002g0057a0001c0001t0002g0060others(5): Show | 8 | HG00280.hp2 HG02486.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225-1054delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218281
|
ATT | A | 10 | a0001c0001t0001g0041a0001c0001t0002g0004a0001c0001t0002g0058others(7): Show | 13 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1225-1055_1225-105 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218281
|
ATTT | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0049others(11): Show | 16 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225-1056_1225-105 others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218281
|
ATTTT | A | 9 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 9 | HG01192.hp1 HG02165.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-1057_1225-105 others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218281
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0002t0001g0249a0001c0002t0001g0269 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1225-1063_1225-105 others(14): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218281
|
ATTTTTTT others(10): Show |
A | 8 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0068others(5): Show | 9 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-1070_1225-105 others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218281
|
ATTTTTTT others(11): Show |
A | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(101): Show | 123 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1225-1071_1225-105 others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | ||||||
chr13:41218299
|
T | C | 5 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG00280.hp1 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1071A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218299 | ||||||
chr13:41218355
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1225-1127G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218355 | ||||||
chr13:41218486
|
A | T | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1225-1258T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218486 | ||||||
chr13:41218504
|
A | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1225-1276T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218504 | ||||||
chr13:41218782
|
T | C | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1225-1554A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218782 | ||||||
chr13:41218842
|
T | TTTTGAGA others(17): Show |
1 | a0001c0002t0001g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1225-1615_1225-161 others(28): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218842 | ||||||
chr13:41218870
|
T | C | 1 | a0001c0002t0001g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1225-1642A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218870 | ||||||
chr13:41219062
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1225-1834C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219062 | ||||||
chr13:41219114
|
AACCCCGT others(25): Show |
A | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 179 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.1225-1918_1225-188 others(36): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219114 | ||||||
chr13:41219119
|
C | T | 2 | a0001c0001t0005g0168a0001c0002t0001g0215 | 2 | HG03041.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1225-1891G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219119 | ||||||
chr13:41219120
|
G | A | 1 | a0002c0003t0001g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1225-1892C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219120 | ||||||
chr13:41219149
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-1921C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219149 | ||||||
chr13:41219290
|
CAA | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1225-2064_1225-206 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219290 | ||||||
chr13:41219308
|
T | C | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1225-2080A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219308 | ||||||
chr13:41219374
|
T | C | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-2146A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219374 | ||||||
chr13:41219598
|
G | C | 6 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(3): Show | 6 | NA18977.hp2 NA19003.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225-2370C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219598 | ||||||
chr13:41219619
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(109): Show | 131 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1225-2391T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219619 | ||||||
chr13:41219673
|
A | T | 1 | a0001c0002t0001g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1225-2445T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219673 | ||||||
chr13:41219674
|
T | A | 1 | a0001c0002t0001g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1225-2446A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219674 | ||||||
chr13:41219695
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1225-2467G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219695 | ||||||
chr13:41219696
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 179 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.1225-2468T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219696 | ||||||
chr13:41219789
|
G | A | 1 | a0002c0003t0001g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1225-2561C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219789 | ||||||
chr13:41219863
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1225-2635A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219863 | ||||||
chr13:41219912
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-2684G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219912 | ||||||
chr13:41219998
|
C | CA | 29 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0049others(26): Show | 34 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1225-2771dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | ||||||
chr13:41219998
|
C | CAA | 76 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 89 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1225-2772_1225-277 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | ||||||
chr13:41219998
|
C | CAAA | 35 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 42 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1225-2773_1225-277 others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | ||||||
chr13:41219998
|
CA | C | 103 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(100): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1225-2771delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | ||||||
chr13:41220125
|
C | T | 29 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(26): Show | 32 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1225-2897G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220125 | ||||||
chr13:41220236
|
A | G | 1 | a0001c0001t0003g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1225-3008T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220236 | ||||||
chr13:41220252
|
C | A | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1224+3004G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220252 | ||||||
chr13:41220322
|
CG | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0041others(55): Show | 63 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1224+2933delC | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220322 | ||||||
chr13:41220323
|
G | GA | 9 | a0001c0001t0003g0031a0001c0001t0003g0035a0001c0006t0003g0036others(6): Show | 9 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1224+2932_1224+293 others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220323 | ||||||
chr13:41220323
|
G | GAA | 3 | a0002c0003t0001g0181a0002c0003t0001g0182a0002c0003t0004g0173 | 3 | HG01981.hp1 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1224+2932_1224+293 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220323 | ||||||
chr13:41220323
|
GGA | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(93): Show | 116 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1224+2931_1224+293 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220323 | ||||||
chr13:41220324
|
G | A | 25 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0002g0059others(22): Show | 25 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1224+2932C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220324 | ||||||
chr13:41220324
|
G | GA | 23 | a0001c0002t0001g0191a0001c0002t0001g0197a0001c0002t0001g0200others(20): Show | 23 | HG00423.hp1 HG00735.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1224+2931dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220324 | ||||||
chr13:41220395
|
G | A | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+2861C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220395 | ||||||
chr13:41220413
|
G | A | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+2843C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220413 | ||||||
chr13:41220615
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1224+2641G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220615 | ||||||
chr13:41220734
|
C | G | 1 | a0001c0001t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1224+2522G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220734 | ||||||
chr13:41221087
|
T | C | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+2169A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221087 | ||||||
chr13:41221156
|
C | CT | 8 | a0001c0001t0002g0059a0001c0002t0001g0024a0001c0002t0001g0218others(5): Show | 9 | HG01261.hp2 HG01515.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1224+2099dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221156 | ||||||
chr13:41221323
|
A | AT | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1224+1932dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221323 | ||||||
chr13:41221425
|
G | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(177): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1224+1831C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221425 | ||||||
chr13:41221448
|
G | A | 5 | a0001c0002t0001g0024a0001c0002t0001g0218a0001c0002t0001g0227others(2): Show | 6 | HG01261.hp2 HG01515.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1224+1808C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221448 | ||||||
chr13:41221599
|
T | C | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1224+1657A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221599 | ||||||
chr13:41221812
|
C | T | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1224+1444G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221812 | ||||||
chr13:41221830
|
T | TACC | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(177): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1224+1425_1224+142 others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221830 | ||||||
chr13:41221886
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1224+1370G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221886 | ||||||
chr13:41222104
|
T | C | 55 | a0001c0001t0001g0021a0001c0001t0001g0151a0001c0001t0001g0152others(52): Show | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1224+1152A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222104 | ||||||
chr13:41222406
|
G | A | 13 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(10): Show | 13 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1224+850C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222406 | ||||||
chr13:41222433
|
A | G | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+823T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222433 | ||||||
chr13:41222486
|
A | C | 10 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+770T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222486 | ||||||
chr13:41222543
|
C | T | 1 | a0001c0001t0006g0087 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1224+713G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222543 | ||||||
chr13:41222676
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 10 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1224+580G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222676 | ||||||
chr13:41222940
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1224+316G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222940 | ||||||
chr13:41223055
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1224+201A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41223055 | ||||||
chr13:41223465
|
A | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(177): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1126-111T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223465 | ||||||
chr13:41223519
|
T | C | 1 | a0001c0002t0001g0272 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1126-165A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223519 | ||||||
chr13:41223536
|
C | T | 18 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(15): Show | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.1126-182G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223536 | ||||||
chr13:41223609
|
T | C | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1126-255A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223609 | ||||||
chr13:41223794
|
C | T | 6 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-440G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223794 | ||||||
chr13:41223798
|
T | C | 6 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-444A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223798 | ||||||
chr13:41223847
|
C | T | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1126-493G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223847 | ||||||
chr13:41224344
|
C | G | 1 | a0001c0002t0001g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1126-990G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224344 | ||||||
chr13:41224408
|
A | G | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-1054T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224408 | ||||||
chr13:41224421
|
T | C | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1126-1067A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224421 | ||||||
chr13:41224439
|
G | A | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1126-1085C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224439 | ||||||
chr13:41224562
|
C | A | 1 | a0003c0004t0001g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1126-1208G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224562 | ||||||
chr13:41224685
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0271 | 3 | HG01515.hp1 HG02004.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1126-1331C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224685 | ||||||
chr13:41224735
|
G | A | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-1381C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224735 | ||||||
chr13:41224784
|
C | T | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-1430G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224784 | ||||||
chr13:41224842
|
T | C | 6 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-1488A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224842 | ||||||
chr13:41225009
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(114): Show | 137 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1125+1423G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225009 | ||||||
chr13:41225038
|
CCCAT | C | 4 | a0001c0002t0001g0189a0001c0002t0001g0199a0001c0002t0001g0200others(1): Show | 4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1390_1125+139 others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225038 | ||||||
chr13:41225105
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1125+1327C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225105 | ||||||
chr13:41225107
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(114): Show | 137 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1125+1325C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225107 | ||||||
chr13:41225209
|
C | CA | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(146): Show | 171 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1125+1222dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225209 | ||||||
chr13:41225209
|
C | CAA | 30 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0028others(27): Show | 33 | HG00280.hp2 HG01109.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1125+1221_1125+122 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225209 | ||||||
chr13:41225229
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1125+1203G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225229 | ||||||
chr13:41225235
|
G | A | 2 | a0001c0002t0001g0234a0001c0002t0001g0272 | 2 | HG00558.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1125+1197C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225235 | ||||||
chr13:41225322
|
G | A | 29 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(26): Show | 32 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1125+1110C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225322 | ||||||
chr13:41225363
|
G | A | 4 | a0001c0002t0001g0189a0001c0002t0001g0199a0001c0002t0001g0200others(1): Show | 4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1069C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225363 | ||||||
chr13:41225520
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1125+912C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225520 | ||||||
chr13:41225808
|
T | TA | 9 | a0001c0001t0005g0168a0001c0002t0001g0201a0001c0002t0001g0256others(6): Show | 9 | HG00280.hp2 HG01192.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+623dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225808 | ||||||
chr13:41225808
|
TA | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 154 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1125+623delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225808 | ||||||
chr13:41225808
|
TAA | T | 26 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 29 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1125+622_1125+623d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225808 | ||||||
chr13:41225951
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1125+481C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225951 | ||||||
chr13:41225959
|
T | TG | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1125+472dupC | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225959 | ||||||
chr13:41225970
|
GAAAAAT | G | 6 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+456_1125+461d others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225970 | ||||||
chr13:41226151
|
G | A | 6 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+281C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41226151 | ||||||
chr13:41226262
|
T | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(109): Show | 131 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1125+170A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41226262 | ||||||
chr13:41226292
|
A | G | 8 | a0001c0002t0001g0014a0001c0002t0001g0025a0001c0002t0001g0240others(5): Show | 11 | HG01952.hp2 HG01993.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1125+140T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41226292 | ||||||
chr13:41226857
|
T | C | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.989-289A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41226857 | ||||||
chr13:41226912
|
G | A | 17 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(14): Show | 20 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(17): Show |
intron_variant | MODIFIER | c.989-344C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41226912 | ||||||
chr13:41227003
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.989-435A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227003 | ||||||
chr13:41227084
|
A | T | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.989-516T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227084 | ||||||
chr13:41227158
|
G | A | 10 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.989-590C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227158 | ||||||
chr13:41227413
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-845C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227413 | ||||||
chr13:41227467
|
T | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(149): Show | 177 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.989-899A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227467 | ||||||
chr13:41227484
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(150): Show | 178 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.989-916T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227484 | ||||||
chr13:41227588
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-1020A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227588 | ||||||
chr13:41227903
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.989-1335G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227903 | ||||||
chr13:41228000
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.989-1432G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228000 | ||||||
chr13:41228002
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.989-1434T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228002 | ||||||
chr13:41228009
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.989-1441C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228009 | ||||||
chr13:41228171
|
CT | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(113): Show | 136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.989-1604delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228171 | ||||||
chr13:41228259
|
G | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0111others(2): Show | 5 | NA18963.hp1 NA18987.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-1691C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228259 | ||||||
chr13:41228308
|
G | A | 2 | a0001c0002t0001g0213a0001c0002t0001g0216 | 2 | NA18969.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.989-1740C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228308 | ||||||
chr13:41228374
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.989-1806G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228374 | ||||||
chr13:41228415
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0071a0001c0001t0001g0083others(1): Show | 5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-1847T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228415 | ||||||
chr13:41228428
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.989-1860C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228428 | ||||||
chr13:41228637
|
TAA | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(150): Show | 178 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.989-2071_989-2070d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228637 | ||||||
chr13:41228710
|
A | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0056 | 3 | HG01070.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.989-2142T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228710 | ||||||
chr13:41228772
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.989-2204C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228772 | ||||||
chr13:41228809
|
A | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-2241T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228809 | ||||||
chr13:41228895
|
T | C | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.989-2327A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228895 | ||||||
chr13:41229021
|
A | G | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.989-2453T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229021 | ||||||
chr13:41229030
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.989-2462A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229030 | ||||||
chr13:41229101
|
C | A | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-2533G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229101 | ||||||
chr13:41229147
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-2579C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229147 | ||||||
chr13:41229235
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.989-2667C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229235 | ||||||
chr13:41229253
|
C | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.989-2685G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229253 | ||||||
chr13:41229543
|
ACT | A | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.989-2977_989-2976d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229543 | ||||||
chr13:41229569
|
G | A | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.989-3001C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229569 | ||||||
chr13:41229685
|
T | A | 25 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(22): Show | 28 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.989-3117A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229685 | ||||||
chr13:41229822
|
C | T | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.989-3254G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229822 | ||||||
chr13:41229850
|
C | T | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.989-3282G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229850 | ||||||
chr13:41229898
|
C | T | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.989-3330G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229898 | ||||||
chr13:41229918
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.989-3350A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229918 | ||||||
chr13:41229950
|
A | G | 1 | a0002c0003t0004g0172 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.989-3382T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229950 | ||||||
chr13:41230013
|
A | C | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3445T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230013 | ||||||
chr13:41230105
|
G | GA | 28 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(25): Show | 35 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.989-3538dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230105 | ||||||
chr13:41230115
|
A | C | 1 | a0001c0002t0001g0253 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.989-3547T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230115 | ||||||
chr13:41230182
|
A | T | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3614T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230182 | ||||||
chr13:41230183
|
T | G | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3615A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230183 | ||||||
chr13:41230325
|
C | T | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.988+3565G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230325 | ||||||
chr13:41230350
|
T | G | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+3540A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230350 | ||||||
chr13:41230563
|
C | CT | 16 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0003g0030others(13): Show | 16 | HG01261.hp1 HG02004.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.988+3326dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230563 | ||||||
chr13:41230625
|
A | C | 1 | a0002c0003t0004g0172 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.988+3265T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230625 | ||||||
chr13:41230684
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(160): Show | 188 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.988+3206T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230684 | ||||||
chr13:41230716
|
G | A | 4 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(1): Show | 4 | HG00558.hp2 NA18953.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+3174C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230716 | ||||||
chr13:41230726
|
C | CT | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(107): Show | 129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.988+3163dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230726 | ||||||
chr13:41230953
|
G | C | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.988+2937C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230953 | ||||||
chr13:41231016
|
G | A | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.988+2874C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231016 | ||||||
chr13:41231029
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.988+2861T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231029 | ||||||
chr13:41231120
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+2770G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231120 | ||||||
chr13:41231206
|
T | G | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.988+2684A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231206 | ||||||
chr13:41231370
|
G | A | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.988+2520C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231370 | ||||||
chr13:41231435
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+2455A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231435 | ||||||
chr13:41231498
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+2392C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231498 | ||||||
chr13:41231618
|
C | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 180 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.988+2272G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231618 | ||||||
chr13:41231739
|
C | G | 1 | a0001c0002t0001g0188 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.988+2151G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231739 | ||||||
chr13:41231878
|
C | CA | 13 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 15 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.988+2011dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231878 | ||||||
chr13:41231878
|
CA | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(142): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.988+2011delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231878 | ||||||
chr13:41231878
|
CAA | C | 6 | a0001c0001t0001g0103a0003c0004t0001g0175a0003c0004t0001g0177others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+2010_988+2011d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231878 | ||||||
chr13:41231897
|
A | G | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.988+1993T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231897 | ||||||
chr13:41231944
|
C | A | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.988+1946G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231944 | ||||||
chr13:41231989
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.988+1901G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231989 | ||||||
chr13:41232042
|
C | T | 25 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(22): Show | 28 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.988+1848G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232042 | ||||||
chr13:41232164
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.988+1726C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232164 | ||||||
chr13:41232192
|
TA | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0230 | 4 | HG00140.hp2 HG03831.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+1697delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232192 | ||||||
chr13:41232324
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.988+1566G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232324 | ||||||
chr13:41232332
|
CAA | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(137): Show | 163 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.988+1556_988+1557d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232332 | ||||||
chr13:41232369
|
G | A | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.988+1521C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232369 | ||||||
chr13:41232374
|
C | T | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+1516G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232374 | ||||||
chr13:41232398
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.988+1492G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232398 | ||||||
chr13:41232547
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.988+1343G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232547 | ||||||
chr13:41232764
|
C | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+1126G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232764 | ||||||
chr13:41233462
|
C | T | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.988+428G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233462 | ||||||
chr13:41233463
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+427C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233463 | ||||||
chr13:41233654
|
C | G | 1 | a0001c0002t0001g0207 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.988+236G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233654 | ||||||
chr13:41233676
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+214G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233676 | ||||||
chr13:41233754
|
C | T | 18 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(15): Show | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.988+136G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233754 | ||||||
chr13:41233814
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.988+76A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233814 | ||||||
chr13:41234204
|
G | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-197C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234204 | ||||||
chr13:41234377
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.871-370G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234377 | ||||||
chr13:41234392
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.871-385A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234392 | ||||||
chr13:41234508
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.871-501C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234508 | ||||||
chr13:41235092
|
A | AT | 10 | a0001c0001t0005g0168a0001c0002t0001g0191a0001c0002t0001g0204others(7): Show | 10 | HG01109.hp1 HG01192.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-1086dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235092 | ||||||
chr13:41235092
|
AT | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(153): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.871-1086delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235092 | ||||||
chr13:41235235
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.871-1228A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235235 | ||||||
chr13:41235335
|
C | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0003g0030others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.871-1328G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235335 | ||||||
chr13:41235814
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0071a0001c0001t0001g0083others(1): Show | 5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-1807G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235814 | ||||||
chr13:41235840
|
G | GAC | 46 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0040others(43): Show | 51 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.871-1835_871-1834d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235840 | ||||||
chr13:41235840
|
G | GACACACA others(13): Show |
1 | a0001c0001t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.871-1834_871-1833i others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235840 | ||||||
chr13:41235854
|
C | CAT | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(108): Show | 130 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.871-1848_871-1847i others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235854 | ||||||
chr13:41235854
|
C | CATAG | 4 | a0001c0001t0001g0015a0001c0001t0001g0071a0001c0001t0001g0083others(1): Show | 5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-1848_871-1847i others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235854 | ||||||
chr13:41235856
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0071a0001c0001t0001g0083others(1): Show | 5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-1849C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235856 | ||||||
chr13:41235956
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0116 | 2 | HG01516.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.871-1949A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235956 | ||||||
chr13:41236001
|
G | A | 23 | a0001c0002t0001g0012a0001c0002t0001g0023a0001c0002t0001g0193others(20): Show | 26 | HG00558.hp2 HG01123.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.871-1994C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236001 | ||||||
chr13:41236046
|
C | G | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.871-2039G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236046 | ||||||
chr13:41236081
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0116 | 2 | HG01516.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.871-2074T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236081 | ||||||
chr13:41236120
|
G | GT | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(106): Show | 128 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.871-2114dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236120 | ||||||
chr13:41236121
|
T | G | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.871-2114A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236121 | ||||||
chr13:41236412
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0068a0001c0001t0001g0158 | 4 | HG01884.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2405G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236412 | ||||||
chr13:41236495
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.871-2488C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236495 | ||||||
chr13:41236598
|
T | G | 3 | a0001c0002t0001g0024a0001c0002t0001g0271a0001c0002t0001g0275 | 4 | HG01515.hp1 HG02004.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2591A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236598 | ||||||
chr13:41236666
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.871-2659T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236666 | ||||||
chr13:41236940
|
C | T | 1 | a0001c0002t0001g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.871-2933G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236940 | ||||||
chr13:41236944
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(179): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.871-2937T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236944 | ||||||
chr13:41236975
|
C | T | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-2968G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236975 | ||||||
chr13:41237166
|
C | A | 2 | a0001c0002t0001g0210a0001c0002t0001g0279 | 2 | NA18962.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.870+3095G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237166 | ||||||
chr13:41237218
|
C | CA | 30 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(27): Show | 34 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.870+3042dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | ||||||
chr13:41237218
|
C | CAA | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(103): Show | 124 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.870+3041_870+3042d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | ||||||
chr13:41237218
|
C | CAAA | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0090others(6): Show | 9 | HG02145.hp2 HG02622.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+3040_870+3042d others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | ||||||
chr13:41237218
|
CA | C | 20 | a0001c0001t0002g0004a0001c0001t0002g0057a0001c0001t0002g0059others(17): Show | 23 | HG02165.hp2 HG03453.hp1 NA18941.hp1 others(20): Show |
intron_variant | MODIFIER | c.870+3042delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | ||||||
chr13:41237306
|
C | G | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+2955G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237306 | ||||||
chr13:41237436
|
AATAAC | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+2820_870+2824d others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237436 | ||||||
chr13:41237462
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(179): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.870+2799G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237462 | ||||||
chr13:41237643
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.870+2618G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237643 | ||||||
chr13:41237646
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.870+2615C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237646 | ||||||
chr13:41237670
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.870+2591G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237670 | ||||||
chr13:41237671
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0145others(5): Show | 11 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.870+2590C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237671 | ||||||
chr13:41237740
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.870+2521G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237740 | ||||||
chr13:41237879
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+2382C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237879 | ||||||
chr13:41237899
|
A | G | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2362T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237899 | ||||||
chr13:41237917
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.870+2344T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237917 | ||||||
chr13:41238081
|
T | C | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+2180A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238081 | ||||||
chr13:41238229
|
G | T | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.870+2032C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238229 | ||||||
chr13:41238280
|
T | A | 1 | a0001c0002t0001g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.870+1981A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238280 | ||||||
chr13:41238301
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.870+1960C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238301 | ||||||
chr13:41238493
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+1768T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238493 | ||||||
chr13:41238635
|
G | A | 25 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(22): Show | 28 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.870+1626C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238635 | ||||||
chr13:41238696
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.870+1565C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238696 | ||||||
chr13:41238890
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.870+1371T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238890 | ||||||
chr13:41238909
|
G | A | 1 | a0001c0002t0001g0026 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.870+1352C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238909 | ||||||
chr13:41238964
|
G | A | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.870+1297C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238964 | ||||||
chr13:41239017
|
T | TA | 11 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0003g0030others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.870+1243dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239017 | ||||||
chr13:41239091
|
G | A | 2 | a0001c0002t0001g0233a0001c0002t0001g0235 | 2 | NA18979.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.870+1170C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239091 | ||||||
chr13:41239353
|
T | A | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.870+908A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239353 | ||||||
chr13:41239359
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.870+902G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239359 | ||||||
chr13:41239363
|
G | A | 16 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(13): Show | 16 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.870+898C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239363 | ||||||
chr13:41239622
|
G | C | 16 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(13): Show | 16 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.870+639C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239622 | ||||||
chr13:41239708
|
T | G | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.870+553A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239708 | ||||||
chr13:41239859
|
C | G | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.870+402G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239859 | ||||||
chr13:41239900
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+361G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239900 | ||||||
chr13:41239958
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.870+303G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239958 | ||||||
chr13:41239978
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.870+283A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239978 | ||||||
chr13:41240032
|
G | A | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.870+229C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240032 | ||||||
chr13:41240117
|
C | T | 1 | a0001c0002t0001g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.870+144G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240117 | ||||||
chr13:41240141
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(148): Show | 176 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.870+120G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240141 | ||||||
chr13:41240162
|
C | CA | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.870+98dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240162 | ||||||
chr13:41240219
|
G | A | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+42C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240219 | ||||||
chr13:41240525
|
G | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG02572.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.698-92C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240525 | ||||||
chr13:41240573
|
TGAA | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-143_698-141del others(3): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240573 | ||||||
chr13:41240668
|
T | A | 10 | a0001c0001t0001g0028a0001c0001t0003g0030a0001c0001t0003g0031others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.698-235A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240668 | ||||||
chr13:41240697
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.698-264T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240697 | ||||||
chr13:41240934
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-501T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240934 | ||||||
chr13:41241157
|
G | T | 1 | a0001c0001t0001g0161 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.698-724C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241157 | ||||||
chr13:41241206
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-773C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241206 | ||||||
chr13:41241248
|
G | A | 6 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(3): Show | 6 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.698-815C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241248 | ||||||
chr13:41241580
|
T | C | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.698-1147A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241580 | ||||||
chr13:41241700
|
G | C | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-1267C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241700 | ||||||
chr13:41241772
|
G | C | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.698-1339C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241772 | ||||||
chr13:41241909
|
A | G | 5 | a0001c0001t0003g0030a0001c0001t0003g0032a0001c0006t0003g0036others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-1476T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241909 | ||||||
chr13:41242105
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(270): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.698-1672A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242105 | ||||||
chr13:41242123
|
C | T | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.698-1690G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242123 | ||||||
chr13:41242126
|
CG | C | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.698-1694delC | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242126 | ||||||
chr13:41242127
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(172): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.698-1694C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242127 | ||||||
chr13:41242127
|
G | GT | 7 | a0001c0002t0001g0190a0001c0002t0001g0193a0001c0002t0001g0203others(4): Show | 7 | HG01123.hp2 HG01496.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.698-1695dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242127 | ||||||
chr13:41242127
|
G | T | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.698-1694C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242127 | ||||||
chr13:41242128
|
T | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.698-1695A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242128 | ||||||
chr13:41242151
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.698-1718G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242151 | ||||||
chr13:41242234
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.698-1801G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242234 | ||||||
chr13:41242245
|
A | G | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1812T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242245 | ||||||
chr13:41242554
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.698-2121G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242554 | ||||||
chr13:41242667
|
G | A | 18 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(15): Show | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-2234C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242667 | ||||||
chr13:41242751
|
T | C | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-2318A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242751 | ||||||
chr13:41242763
|
G | A | 1 | a0002c0003t0004g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.698-2330C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242763 | ||||||
chr13:41242784
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.698-2351G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242784 | ||||||
chr13:41242787
|
C | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-2354G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242787 | ||||||
chr13:41242849
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(164): Show | 192 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.698-2416A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242849 | ||||||
chr13:41242852
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0125 | 2 | HG01934.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.698-2419C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242852 | ||||||
chr13:41242941
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.698-2508A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242941 | ||||||
chr13:41243017
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(176): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.698-2584C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243017 | ||||||
chr13:41243103
|
C | T | 18 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(15): Show | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-2670G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243103 | ||||||
chr13:41243108
|
A | C | 1 | a0001c0002t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.698-2675T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243108 | ||||||
chr13:41243129
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.698-2696C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243129 | ||||||
chr13:41243168
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(158): Show | 186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.698-2735T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243168 | ||||||
chr13:41243238
|
A | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(161): Show | 189 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.698-2805T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243238 | ||||||
chr13:41243404
|
C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 134 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.698-2972dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243404 | ||||||
chr13:41243404
|
C | CAA | 8 | a0001c0001t0001g0081a0001c0001t0001g0127a0001c0001t0001g0130others(5): Show | 8 | HG00438.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-2973_698-2972d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243404 | ||||||
chr13:41243404
|
CA | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(34): Show | 42 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.698-2972delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243404 | ||||||
chr13:41243484
|
G | A | 10 | a0001c0001t0001g0028a0001c0001t0003g0030a0001c0001t0003g0031others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.698-3051C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243484 | ||||||
chr13:41243513
|
C | G | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-3080G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243513 | ||||||
chr13:41243515
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.698-3082C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243515 | ||||||
chr13:41243523
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.698-3090G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243523 | ||||||
chr13:41243973
|
C | T | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.698-3540G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243973 | ||||||
chr13:41243977
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.698-3544A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243977 | ||||||
chr13:41244123
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.698-3690G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244123 | ||||||
chr13:41244140
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(179): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.698-3707A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244140 | ||||||
chr13:41244166
|
T | C | 1 | a0001c0002t0001g0206 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.698-3733A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244166 | ||||||
chr13:41244220
|
ACTTT | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.698-3791_698-3788d others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244220 | ||||||
chr13:41244238
|
A | T | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-3805T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244238 | ||||||
chr13:41244292
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-3859G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244292 | ||||||
chr13:41244326
|
C | T | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-3893G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244326 | ||||||
chr13:41244407
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.698-3974C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244407 | ||||||
chr13:41244460
|
T | G | 3 | a0001c0001t0005g0168a0002c0003t0001g0181a0002c0003t0001g0182 | 3 | HG01981.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.698-4027A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244460 | ||||||
chr13:41244464
|
C | T | 18 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(15): Show | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-4031G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244464 | ||||||
chr13:41244608
|
A | C | 4 | a0001c0002t0001g0189a0001c0002t0001g0199a0001c0002t0001g0200others(1): Show | 4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-4175T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244608 | ||||||
chr13:41244665
|
C | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-4232G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244665 | ||||||
chr13:41244738
|
T | G | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-4305A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244738 | ||||||
chr13:41244748
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.698-4315T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244748 | ||||||
chr13:41244756
|
G | C | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-4323C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244756 | ||||||
chr13:41244807
|
C | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 4 | HG00544.hp2 NA18953.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.698-4374G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244807 | ||||||
chr13:41244833
|
A | G | 18 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(15): Show | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-4400T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244833 | ||||||
chr13:41244841
|
C | T | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.698-4408G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244841 | ||||||
chr13:41245004
|
C | G | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-4571G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245004 | ||||||
chr13:41245228
|
A | G | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.698-4795T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245228 | ||||||
chr13:41245249
|
C | CT | 119 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(116): Show | 139 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.698-4817dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245249 | ||||||
chr13:41245259
|
T | C | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-4826A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245259 | ||||||
chr13:41245405
|
T | C | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.698-4972A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245405 | ||||||
chr13:41245618
|
T | C | 1 | a0001c0002t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.698-5185A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245618 | ||||||
chr13:41245751
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.698-5318A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245751 | ||||||
chr13:41246044
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0166 | 3 | NA18945.hp1 NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.698-5611C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246044 | ||||||
chr13:41246049
|
CT | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.698-5617delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246049 | ||||||
chr13:41246069
|
C | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-5636G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246069 | ||||||
chr13:41246102
|
T | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0128a0001c0001t0001g0129 | 4 | HG01934.hp1 HG02083.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-5669A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246102 | ||||||
chr13:41246241
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.698-5808A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246241 | ||||||
chr13:41246255
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.698-5822C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246255 | ||||||
chr13:41246578
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.697+6067A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246578 | ||||||
chr13:41246590
|
T | G | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.697+6055A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246590 | ||||||
chr13:41246675
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0130 | 2 | HG00558.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.697+5970A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246675 | ||||||
chr13:41246766
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.697+5879G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246766 | ||||||
chr13:41246824
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.697+5821T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246824 | ||||||
chr13:41246834
|
G | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.697+5811C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246834 | ||||||
chr13:41246867
|
C | T | 4 | a0001c0001t0005g0168a0002c0003t0001g0181a0002c0003t0001g0182others(1): Show | 4 | HG01981.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+5778G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246867 | ||||||
chr13:41246939
|
C | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.697+5706G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246939 | ||||||
chr13:41247032
|
T | C | 1 | a0001c0002t0001g0241 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.697+5613A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247032 | ||||||
chr13:41247041
|
T | A | 1 | a0001c0002t0001g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.697+5604A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247041 | ||||||
chr13:41247143
|
C | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.697+5502G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247143 | ||||||
chr13:41247144
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.697+5501C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247144 | ||||||
chr13:41247168
|
G | A | 24 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(21): Show | 27 | HG00544.hp1 HG00738.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.697+5477C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247168 | ||||||
chr13:41247215
|
C | T | 9 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.697+5430G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247215 | ||||||
chr13:41247228
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0102a0001c0001t0001g0131others(3): Show | 7 | HG00423.hp2 NA18939.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.697+5417A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247228 | ||||||
chr13:41247384
|
A | G | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697+5261T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247384 | ||||||
chr13:41247605
|
A | T | 3 | a0001c0006t0003g0036a0001c0006t0003g0038a0001c0006t0003g0039 | 3 | HG02559.hp2 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.697+5040T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247605 | ||||||
chr13:41247812
|
G | GA | 8 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 10 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.697+4832dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247812 | ||||||
chr13:41247889
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.697+4756T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247889 | ||||||
chr13:41248060
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.697+4585G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248060 | ||||||
chr13:41248133
|
T | C | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697+4512A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248133 | ||||||
chr13:41248166
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.697+4479G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248166 | ||||||
chr13:41248225
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+4420C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248225 | ||||||
chr13:41248268
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.697+4377G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248268 | ||||||
chr13:41248315
|
T | C | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+4330A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248315 | ||||||
chr13:41248634
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.697+4011G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248634 | ||||||
chr13:41248652
|
G | C | 4 | a0001c0002t0001g0194a0001c0002t0001g0207a0001c0002t0001g0208others(1): Show | 4 | NA18939.hp2 NA18972.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3993C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248652 | ||||||
chr13:41248668
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.697+3977C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248668 | ||||||
chr13:41248734
|
C | T | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3911G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248734 | ||||||
chr13:41248779
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.697+3866C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248779 | ||||||
chr13:41248840
|
A | G | 3 | a0001c0001t0001g0037a0002c0008t0001g0277a0002c0008t0001g0278 | 3 | HG01069.hp1 HG01071.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.697+3805T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248840 | ||||||
chr13:41248842
|
T | C | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3803A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248842 | ||||||
chr13:41249094
|
C | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.697+3551G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249094 | ||||||
chr13:41249099
|
CTA | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.697+3544_697+3545d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249099 | ||||||
chr13:41249243
|
A | G | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697+3402T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249243 | ||||||
chr13:41249264
|
G | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0104 | 2 | HG01433.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.697+3381C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249264 | ||||||
chr13:41249269
|
C | T | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+3376G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249269 | ||||||
chr13:41249289
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.697+3356G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249289 | ||||||
chr13:41249294
|
T | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0003g0030others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.697+3351A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249294 | ||||||
chr13:41249304
|
G | A | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3341C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249304 | ||||||
chr13:41249619
|
C | CT | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(89): Show | 111 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.697+3025dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | ||||||
chr13:41249619
|
C | CTT | 49 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0029others(46): Show | 53 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.697+3024_697+3025d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | ||||||
chr13:41249619
|
C | CTTT | 8 | a0001c0001t0001g0091a0001c0001t0002g0048a0001c0001t0002g0057others(5): Show | 8 | HG01192.hp1 HG02135.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+3023_697+3025d others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | ||||||
chr13:41249619
|
C | T | 3 | a0001c0001t0001g0037a0005c0007t0001g0045a0005c0007t0001g0046 | 3 | HG02622.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.697+3026G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | ||||||
chr13:41249619
|
CT | C | 90 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(87): Show | 116 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.697+3025delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | ||||||
chr13:41249619
|
CTTTTTT | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+3020_697+3025d others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | ||||||
chr13:41249626
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.697+3019A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249626 | ||||||
chr13:41249628
|
T | C | 6 | a0001c0002t0001g0024a0001c0002t0001g0218a0001c0002t0001g0227others(3): Show | 7 | HG01261.hp2 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.697+3017A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249628 | ||||||
chr13:41249664
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.697+2981A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249664 | ||||||
chr13:41249778
|
T | C | 56 | a0001c0001t0001g0021a0001c0001t0001g0151a0001c0001t0001g0152others(53): Show | 68 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.697+2867A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249778 | ||||||
chr13:41250165
|
G | A | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+2480C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250165 | ||||||
chr13:41250258
|
T | C | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | NA18967.hp2 NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.697+2387A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250258 | ||||||
chr13:41250497
|
A | T | 4 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0173others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.697+2148T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250497 | ||||||
chr13:41250497
|
AT | A | 11 | a0001c0001t0001g0051a0001c0001t0001g0080a0001c0001t0001g0139others(8): Show | 11 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.697+2147delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250497 | ||||||
chr13:41250527
|
C | T | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.697+2118G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250527 | ||||||
chr13:41250597
|
G | T | 4 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0173others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.697+2048C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250597 | ||||||
chr13:41250618
|
C | T | 8 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(5): Show | 8 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.697+2027G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250618 | ||||||
chr13:41250645
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.697+2000G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250645 | ||||||
chr13:41250648
|
C | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0056 | 3 | HG01070.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.697+1997G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250648 | ||||||
chr13:41250699
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.697+1946C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250699 | ||||||
chr13:41250700
|
G | A | 1 | a0001c0002t0001g0210 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.697+1945C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250700 | ||||||
chr13:41250731
|
G | T | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.697+1914C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250731 | ||||||
chr13:41250972
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.697+1673T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250972 | ||||||
chr13:41251356
|
T | C | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.697+1289A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251356 | ||||||
chr13:41251359
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(179): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.697+1286G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251359 | ||||||
chr13:41251404
|
A | G | 1 | a0005c0007t0001g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.697+1241T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251404 | ||||||
chr13:41251534
|
A | G | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.697+1111T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251534 | ||||||
chr13:41251609
|
G | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0003g0030others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.697+1036C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251609 | ||||||
chr13:41251728
|
T | A | 12 | a0001c0002t0001g0012a0001c0002t0001g0211a0001c0002t0001g0212others(9): Show | 14 | HG00558.hp2 HG02015.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.697+917A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251728 | ||||||
chr13:41251929
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.697+716C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251929 | ||||||
chr13:41252114
|
A | T | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+531T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252114 | ||||||
chr13:41252308
|
T | TATAA | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.697+333_697+336dup others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252308 | ||||||
chr13:41252390
|
C | A | 1 | a0001c0002t0002g0223 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.697+255G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252390 | ||||||
chr13:41252543
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.697+102T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252543 | ||||||
chr13:41252858
|
C | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.589+91G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 4/9 | chr13 | 41252858 | ||||||
chr13:41252905
|
A | C | 2 | a0001c0002t0001g0240a0001c0002t0001g0241 | 2 | HG02080.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.589+44T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 4/9 | chr13 | 41252905 | ||||||
chr13:41253142
|
T | C | 1 | a0001c0002t0001g0271 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.508-112A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253142 | ||||||
chr13:41253340
|
G | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.508-310C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253340 | ||||||
chr13:41253342
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.508-312A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253342 | ||||||
chr13:41253344
|
A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0029others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.508-314T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253344 | ||||||
chr13:41253434
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(179): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.508-404A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253434 | ||||||
chr13:41253653
|
A | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.508-623T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253653 | ||||||
chr13:41253679
|
G | C | 1 | a0001c0002t0001g0218 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.508-649C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253679 | ||||||
chr13:41254091
|
T | C | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.507+438A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254091 | ||||||
chr13:41254209
|
CCTCTT | C | 18 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(15): Show | 21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+315_507+319del others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254209 | ||||||
chr13:41254250
|
G | A | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.507+279C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254250 | ||||||
chr13:41254293
|
T | C | 1 | a0002c0003t0001g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.507+236A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254293 | ||||||
chr13:41254303
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.507+226G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254303 | ||||||
chr13:41254378
|
A | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+151T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254378 | ||||||
chr13:41254507
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507+22A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254507 | ||||||
chr13:41255034
|
A | G | 2 | a0001c0002t0001g0238a0001c0002t0001g0239 | 2 | NA19009.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.416-414T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255034 | ||||||
chr13:41255354
|
T | C | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-734A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255354 | ||||||
chr13:41255388
|
G | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(12): Show | 20 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-768C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255388 | ||||||
chr13:41255447
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.416-827A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255447 | ||||||
chr13:41255466
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.416-846G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255466 | ||||||
chr13:41255565
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(118): Show | 143 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.416-945C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255565 | ||||||
chr13:41255671
|
G | A | 15 | a0002c0003t0001g0181a0002c0003t0001g0182a0002c0003t0004g0170others(12): Show | 15 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.416-1051C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255671 | ||||||
chr13:41255721
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.416-1101G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255721 | ||||||
chr13:41255766
|
G | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0030others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-1146C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255766 | ||||||
chr13:41255817
|
C | A | 1 | a0001c0002t0001g0228 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.416-1197G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255817 | ||||||
chr13:41255947
|
C | T | 20 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(17): Show | 23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-1327G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255947 | ||||||
chr13:41255960
|
T | A | 20 | a0002c0003t0001g0181a0002c0003t0001g0182a0002c0003t0004g0170others(17): Show | 20 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.416-1340A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255960 | ||||||
chr13:41256124
|
C | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(123): Show | 147 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.416-1504G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256124 | ||||||
chr13:41256328
|
AT | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(156): Show | 183 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.416-1709delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256328 | ||||||
chr13:41256350
|
G | A | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1730C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256350 | ||||||
chr13:41256387
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(173): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.416-1767A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256387 | ||||||
chr13:41256388
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.416-1768C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256388 | ||||||
chr13:41256614
|
G | A | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1994C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256614 | ||||||
chr13:41256622
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.416-2002G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256622 | ||||||
chr13:41256654
|
CCA | C | 10 | a0001c0001t0001g0029a0001c0001t0003g0030a0001c0001t0003g0031others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-2036_416-2035d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256654 | ||||||
chr13:41256741
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.416-2121G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256741 | ||||||
chr13:41256770
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-2150C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256770 | ||||||
chr13:41256808
|
T | C | 2 | a0002c0003t0001g0181a0002c0003t0001g0182 | 2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.416-2188A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256808 | ||||||
chr13:41256826
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.416-2206A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256826 | ||||||
chr13:41256906
|
G | A | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.416-2286C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256906 | ||||||
chr13:41256976
|
A | G | 20 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(17): Show | 23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-2356T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256976 | ||||||
chr13:41257125
|
A | G | 1 | a0001c0002t0001g0188 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.416-2505T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257125 | ||||||
chr13:41257134
|
G | A | 3 | a0001c0001t0005g0168a0001c0002t0001g0227a0001c0002t0001g0228 | 3 | HG01261.hp2 HG01516.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.416-2514C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257134 | ||||||
chr13:41257335
|
A | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.416-2715T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257335 | ||||||
chr13:41257508
|
A | C | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.416-2888T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257508 | ||||||
chr13:41257720
|
T | G | 1 | a0002c0003t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.415+2773A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257720 | ||||||
chr13:41257909
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.415+2584G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257909 | ||||||
chr13:41258147
|
T | C | 4 | a0004c0005t0001g0183a0004c0005t0001g0184a0004c0005t0001g0185others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+2346A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258147 | ||||||
chr13:41258224
|
G | A | 20 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(17): Show | 23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+2269C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258224 | ||||||
chr13:41258404
|
C | T | 1 | a0001c0002t0001g0188 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.415+2089G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258404 | ||||||
chr13:41258498
|
G | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.415+1995C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258498 | ||||||
chr13:41258569
|
A | C | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.415+1924T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258569 | ||||||
chr13:41258574
|
A | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(8): Show | 14 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.415+1919T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258574 | ||||||
chr13:41258575
|
C | A | 21 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(18): Show | 24 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.415+1918G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258575 | ||||||
chr13:41258575
|
CA | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 159 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.415+1917delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258575 | ||||||
chr13:41258576
|
A | C | 21 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(18): Show | 24 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.415+1917T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258576 | ||||||
chr13:41258577
|
A | AAC | 19 | a0002c0003t0001g0181a0002c0003t0001g0182a0002c0003t0004g0170others(16): Show | 19 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.415+1915_415+1916i others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258577 | ||||||
chr13:41258577
|
A | T | 2 | a0001c0002t0001g0236a0001c0002t0001g0237 | 2 | HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.415+1916T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258577 | ||||||
chr13:41258870
|
A | T | 10 | a0001c0001t0001g0029a0001c0001t0003g0030a0001c0001t0003g0031others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+1623T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258870 | ||||||
chr13:41258928
|
A | T | 1 | a0001c0001t0002g0066 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.415+1565T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258928 | ||||||
chr13:41259121
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.415+1372A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259121 | ||||||
chr13:41259131
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18955.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.415+1362G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259131 | ||||||
chr13:41259203
|
C | G | 20 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(17): Show | 23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+1290G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259203 | ||||||
chr13:41259205
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(172): Show | 201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.415+1288T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259205 | ||||||
chr13:41259209
|
C | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.415+1284G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259209 | ||||||
chr13:41259273
|
T | A | 1 | a0001c0002t0001g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.415+1220A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259273 | ||||||
chr13:41259432
|
G | A | 5 | a0003c0004t0001g0175a0003c0004t0001g0177a0003c0004t0001g0178others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+1061C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259432 | ||||||
chr13:41259463
|
G | A | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(5): Show | 8 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1030C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259463 | ||||||
chr13:41259487
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(173): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.415+1006T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259487 | ||||||
chr13:41259541
|
A | C | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.415+952T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259541 | ||||||
chr13:41259619
|
G | A | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.415+874C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259619 | ||||||
chr13:41259701
|
C | CA | 10 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0266others(7): Show | 10 | HG00280.hp2 HG01952.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+791dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | ||||||
chr13:41259701
|
C | CAA | 9 | a0002c0003t0004g0173a0002c0003t0004g0174a0002c0008t0001g0277others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+790_415+791dup others(2): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | ||||||
chr13:41259701
|
C | CAAAAAAA others(14): Show |
11 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(8): Show | 14 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.415+791_415+792ins others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | ||||||
chr13:41259701
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0002g0066 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.415+791_415+792ins others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | ||||||
chr13:41259702
|
A | AAAAAAAA others(15): Show |
10 | a0001c0001t0001g0029a0001c0001t0003g0030a0001c0001t0003g0031others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+790_415+791ins others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259702 | ||||||
chr13:41259702
|
A | AAAAAAAC others(16): Show |
114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(111): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.415+790_415+791ins others(23): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259702 | ||||||
chr13:41259712
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.415+780_415+781ins others(24): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | ||||||
chr13:41259712
|
A | AAAAAAAA others(18): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.415+780_415+781ins others(25): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | ||||||
chr13:41259712
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0056 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.415+780_415+781ins others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | ||||||
chr13:41259712
|
A | AAAAAAAA others(17): Show |
2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.415+780_415+781ins others(24): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | ||||||
chr13:41259712
|
A | AAAAAAAC others(14): Show |
7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 7 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.415+780_415+781ins others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | ||||||
chr13:41259712
|
A | AAAAAACA others(15): Show |
1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.415+780_415+781ins others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | ||||||
chr13:41259712
|
A | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(133): Show | 160 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.415+781T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | ||||||
chr13:41259785
|
A | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.415+708T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259785 | ||||||
chr13:41259865
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.415+628C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259865 | ||||||
chr13:41260057
|
G | A | 4 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0235others(1): Show | 4 | HG00558.hp2 NA18953.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+436C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260057 | ||||||
chr13:41260123
|
A | G | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.415+370T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260123 | ||||||
chr13:41260220
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.415+273G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260220 | ||||||
chr13:41260221
|
G | T | 5 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+272C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260221 | ||||||
chr13:41260271
|
G | A | 1 | a0001c0002t0001g0269 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415+222C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260271 | ||||||
chr13:41260442
|
G | GT | 13 | a0001c0001t0002g0004a0001c0001t0002g0048a0001c0001t0002g0057others(10): Show | 16 | HG02165.hp2 NA18952.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+50dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260442 | ||||||
chr13:41260442
|
GT | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(109): Show | 133 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.415+50delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260442 | ||||||
chr13:41260940
|
T | TA | 176 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(173): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.-8-26dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41260940 | ||||||
chr13:41260953
|
T | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(173): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.-8-38A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41260953 | ||||||
chr13:41260970
|
A | G | 62 | a0001c0002t0001g0003a0001c0002t0001g0011a0001c0002t0001g0012others(59): Show | 73 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-8-55T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41260970 | ||||||
chr13:41261210
|
T | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02080.hp2 HG02165.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-8-295A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261210 | ||||||
chr13:41261269
|
G | A | 22 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(19): Show | 25 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-354C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261269 | ||||||
chr13:41261370
|
CATAATTC others(2): Show |
C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.-8-464_-8-456delAA others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261370 | ||||||
chr13:41261593
|
C | T | 13 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(10): Show | 13 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-678G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261593 | ||||||
chr13:41261676
|
A | G | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-761T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261676 | ||||||
chr13:41261988
|
T | C | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-8-1073A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261988 | ||||||
chr13:41261990
|
T | TA | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(123): Show | 147 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.-8-1076dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261990 | ||||||
chr13:41261990
|
T | TAA | 51 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(48): Show | 56 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.-8-1077_-8-1076dup others(2): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261990 | ||||||
chr13:41262036
|
T | A | 1 | a0001c0002t0001g0271 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-1121A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262036 | ||||||
chr13:41262061
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(111): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-8-1146C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262061 | ||||||
chr13:41262075
|
G | A | 2 | a0005c0007t0001g0045a0005c0007t0001g0046 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-8-1160C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262075 | ||||||
chr13:41262093
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(110): Show | 134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-8-1178A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262093 | ||||||
chr13:41262103
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(120): Show | 146 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8-1188C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262103 | ||||||
chr13:41262107
|
C | T | 20 | a0002c0003t0001g0181a0002c0003t0001g0182a0002c0003t0004g0170others(17): Show | 20 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-1192G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262107 | ||||||
chr13:41262193
|
A | T | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(5): Show | 8 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1278T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262193 | ||||||
chr13:41262328
|
C | T | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-9+1157G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262328 | ||||||
chr13:41262338
|
C | CA | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(104): Show | 126 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-9+1146dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | ||||||
chr13:41262338
|
C | CAA | 13 | a0001c0001t0001g0010a0001c0001t0001g0157a0001c0001t0001g0158others(10): Show | 15 | HG01346.hp2 HG02071.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+1145_-9+1146dup others(2): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | ||||||
chr13:41262338
|
CA | C | 6 | a0002c0003t0004g0170a0002c0003t0004g0171a0002c0003t0004g0172others(3): Show | 6 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1146delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | ||||||
chr13:41262338
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9+1135_-9+1146del others(12): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | ||||||
chr13:41262351
|
A | G | 1 | a0007c0011t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-9+1134T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262351 | ||||||
chr13:41262358
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-9+1127C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262358 | ||||||
chr13:41262358
|
GA | G | 18 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 21 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+1126delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262358 | ||||||
chr13:41262359
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+1126T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262359 | ||||||
chr13:41262467
|
G | T | 1 | a0001c0001t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-9+1018C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262467 | ||||||
chr13:41262644
|
G | GA | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.-9+840dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262644 | ||||||
chr13:41262689
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-9+796T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262689 | ||||||
chr13:41262968
|
G | A | 2 | a0002c0008t0001g0277a0002c0008t0001g0278 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-9+517C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262968 | ||||||
chr13:41262990
|
G | A | 20 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(17): Show | 23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-9+495C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262990 | ||||||
chr13:41263019
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(111): Show | 135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-9+466A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263019 | ||||||
chr13:41263068
|
C | A | 1 | a0001c0002t0001g0279 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-9+417G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263068 | ||||||
chr13:41263084
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 181 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.-9+401G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263084 | ||||||
chr13:41263476
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-9+9A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263476 |