geneid | 283578 |
---|---|
ensemblid | ENSG00000100580.8 |
hgncid | 18633 |
symbol | TMED8 |
name | transmembrane p24 trafficking protein family member 8 |
refseq_nuc | NM_213601.3 |
refseq_prot | NP_998766.1 |
ensembl_nuc | ENST00000216468.8 |
ensembl_prot | ENSP00000216468.7 |
mane_status | MANE Select |
chr | chr14 |
start | 77335029 |
end | 77377094 |
strand | - |
ver | v1.2 |
region | chr14:77335029-77377094 |
region5000 | chr14:77330029-77382094 |
regionname0 | TMED8_chr14_77335029_77377094 |
regionname5000 | TMED8_chr14_77330029_77382094 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 325 | 211 | 39 | 35 | 119 | 4 | 12 | 90 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002 | 0/0 | 325 | 64 | 35 | 9 | 5 | 5 | 10 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003 | 0/0 | 325 | 49 | 11 | 18 | 1 | 7 | 12 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0004 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0005 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0006 | 0/0 | 325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0007 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 978 | 207 | 36 | 34 | 119 | 4 | 12 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0002 | 0/0 | 978 | 61 | 33 | 8 | 5 | 5 | 10 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0003 | 0/0 | 978 | 49 | 11 | 18 | 1 | 7 | 12 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0004 | 0/0 | 978 | 3 | 2 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0005 | 0/0 | 978 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0006 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0007 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0008 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0009 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0010 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
c0011 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 6792 | 80 | 1 | 14 | 52 | 4 | 8 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0002 | 0/0 | 6793 | 40 | 6 | 4 | 27 | 0 | 3 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0003 | 0/0 | 6783 | 32 | 2 | 15 | 5 | 5 | 5 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0004 | 0/0 | 6794 | 25 | 2 | 9 | 12 | 1 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0005 | 0/0 | 6792 | 18 | 14 | 0 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0006 | 0/0 | 6794 | 15 | 7 | 3 | 1 | 2 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0007 | 0/0 | 6786 | 13 | 1 | 3 | 6 | 2 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0008 | 0/0 | 6791 | 12 | 10 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0009 | 0/0 | 6792 | 10 | 9 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0010 | 0/0 | 6792 | 7 | 7 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0011 | 0/0 | 6790 | 5 | 0 | 2 | 0 | 0 | 3 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0012 | 0/0 | 6792 | 4 | 4 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0013 | 0/0 | 6793 | 4 | 3 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0014 | 0/0 | 6793 | 4 | 0 | 0 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0015 | 0/0 | 6783 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0016 | 0/0 | 6783 | 3 | 0 | 0 | 0 | 0 | 3 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0017 | 0/0 | 6792 | 3 | 0 | 2 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0018 | 0/0 | 6792 | 3 | 0 | 0 | 3 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0019 | 0/0 | 6792 | 3 | 0 | 0 | 3 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0020 | 0/0 | 6789 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0021 | 0/0 | 6792 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0022 | 0/0 | 6792 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0023 | 0/0 | 6792 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0024 | 0/0 | 6792 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0025 | 0/0 | 6794 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0026 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0027 | 0/0 | 6793 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0028 | 0/0 | 6791 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0029 | 0/0 | 6791 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0030 | 0/0 | 6785 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0031 | 0/0 | 6791 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0032 | 0/0 | 6791 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0033 | 0/0 | 6791 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0034 | 0/0 | 6783 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0035 | 0/0 | 6783 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0036 | 0/0 | 6791 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0037 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0038 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0039 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0040 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0041 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0042 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0043 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0044 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0045 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0046 | 0/0 | 6820 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0047 | 1/0 | 6784 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0048 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0049 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0050 | 0/0 | 6784 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0051 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0052 | 0/0 | 6793 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0053 | 0/0 | 6785 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0054 | 0/0 | 6794 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0055 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
t0056 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0266 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 978 | 207 | 36 | 34 | 119 | 4 | 12 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0005 | 0/0 | 978 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0008 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0009 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002 | 0/0 | 978 | 61 | 33 | 8 | 5 | 5 | 10 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0004 | 0/0 | 978 | 3 | 2 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003 | 0/0 | 978 | 49 | 11 | 18 | 1 | 7 | 12 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0004c0007 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0005c0010 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0006c0011 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0007c0006 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7769 | 60 | 0 | 11 | 46 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0002 | 0/0 | 7770 | 36 | 4 | 4 | 27 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0003 | 0/0 | 7760 | 5 | 0 | 1 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0004 | 0/0 | 7771 | 23 | 0 | 9 | 12 | 1 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0005 | 0/0 | 7769 | 9 | 5 | 0 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0006 | 0/0 | 7771 | 12 | 4 | 3 | 1 | 2 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0007 | 0/0 | 7763 | 7 | 0 | 0 | 6 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0008 | 0/0 | 7768 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0010 | 0/0 | 7769 | 7 | 7 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0011 | 0/0 | 7767 | 5 | 0 | 2 | 0 | 0 | 3 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0012 | 0/0 | 7769 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0014 | 0/0 | 7770 | 4 | 0 | 0 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0015 | 0/0 | 7760 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0018 | 0/0 | 7769 | 3 | 0 | 0 | 3 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0019 | 0/0 | 7769 | 3 | 0 | 0 | 3 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0020 | 0/0 | 7766 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0023 | 0/0 | 7769 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0025 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0026 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0027 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0028 | 0/0 | 7768 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0031 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0033 | 0/0 | 7768 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0036 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0038 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0040 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0043 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0044 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0045 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0046 | 0/0 | 7797 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0047 | 1/0 | 7761 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0050 | 0/0 | 7761 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0051 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0052 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0054 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0055 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0001t0056 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0005t0024 | 0/0 | 7769 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0008t0032 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0001c0009t0013 | 0/0 | 7770 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0001 | 0/0 | 7769 | 19 | 1 | 3 | 5 | 4 | 6 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0002 | 0/0 | 7770 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0003 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0005 | 0/0 | 7769 | 5 | 5 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0006 | 0/0 | 7771 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0008 | 0/0 | 7768 | 10 | 8 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0009 | 0/0 | 7769 | 10 | 9 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0012 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0017 | 0/0 | 7769 | 3 | 0 | 2 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0022 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0029 | 0/0 | 7768 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0037 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0039 | 0/0 | 7769 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0041 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0042 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0049 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0002t0053 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0002c0004t0013 | 0/0 | 7770 | 3 | 2 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0002 | 0/0 | 7770 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0003 | 0/0 | 7760 | 26 | 2 | 13 | 1 | 5 | 5 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0004 | 0/0 | 7771 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0005 | 0/0 | 7769 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0006 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0007 | 0/0 | 7763 | 6 | 1 | 3 | 0 | 1 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0016 | 0/0 | 7760 | 3 | 0 | 0 | 0 | 0 | 3 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0021 | 0/0 | 7769 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0022 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0030 | 0/0 | 7762 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0034 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0003c0003t0035 | 0/0 | 7760 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0004c0007t0048 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0005c0010t0025 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0006c0011t0001 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
a0007c0006t0005 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | copy fasta | chr14 | 77330029 | 77382094 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0011g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0011g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0011g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0012g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0014g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0014g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0014g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0014g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0015g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0015g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0015g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0018g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0018g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0018g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0019g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0019g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0020g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0020g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0020g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0023g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0023g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0025g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0026g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0027g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0028g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0031g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0033g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0036g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0038g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0040g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0043g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0044g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0045g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0046g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0047g0266 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0050g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0051g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0052g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0054g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0055g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0001t0056g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0005t0024g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0005t0024g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0008t0032g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0001c0009t0013g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0017g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0017g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0017g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0022g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0029g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0037g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0039g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0041g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0042g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0049g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0002t0053g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0004t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0004t0013g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0002c0004t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0007g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0016g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0016g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0016g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0021g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0021g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0022g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0030g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0034g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0003c0003t0035g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0004c0007t0048g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0005c0010t0025g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0006c0011t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
a0007c0006t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0023 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00099 | hp2 | a0003 | c0003 | t0003 | g0090 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00140 | hp1 | a0003 | c0003 | t0007 | g0077 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00140 | hp2 | a0003 | c0003 | t0003 | g0003 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0200 | EUR | FIN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0026 | EUR | FIN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00597 | hp1 | a0001 | c0001 | t0014 | g0316 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00639 | hp1 | a0003 | c0003 | t0003 | g0083 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00642 | hp1 | a0003 | c0003 | t0003 | g0085 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00642 | hp2 | a0002 | c0002 | t0017 | g0040 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00733 | hp1 | a0003 | c0003 | t0007 | g0002 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00735 | hp1 | a0002 | c0002 | t0017 | g0043 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00738 | hp1 | a0003 | c0003 | t0003 | g0003 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00741 | hp1 | a0003 | c0003 | t0003 | g0098 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01069 | hp2 | a0003 | c0003 | t0007 | g0073 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01071 | hp2 | a0001 | c0001 | t0011 | g0191 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01081 | hp1 | a0001 | c0001 | t0056 | g0192 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01081 | hp2 | a0002 | c0004 | t0013 | g0014 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01106 | hp1 | a0003 | c0003 | t0003 | g0114 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01106 | hp2 | a0001 | c0001 | t0051 | g0171 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01109 | hp2 | a0001 | c0005 | t0024 | g0315 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01167 | hp1 | a0003 | c0003 | t0021 | g0081 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01167 | hp2 | a0003 | c0003 | t0003 | g0084 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01169 | hp1 | a0003 | c0003 | t0003 | g0086 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0197 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01175 | hp1 | a0002 | c0002 | t0041 | g0028 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01243 | hp1 | a0003 | c0003 | t0007 | g0076 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01243 | hp2 | a0002 | c0002 | t0009 | g0045 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01255 | hp1 | a0003 | c0003 | t0003 | g0097 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01255 | hp2 | a0001 | c0001 | t0011 | g0189 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01258 | hp2 | a0003 | c0003 | t0003 | g0106 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0194 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0018 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01515 | hp2 | a0003 | c0003 | t0003 | g0096 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01516 | hp1 | a0003 | c0003 | t0030 | g0075 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01516 | hp2 | a0003 | c0003 | t0003 | g0004 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01517 | hp2 | a0003 | c0003 | t0003 | g0004 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01884 | hp1 | a0001 | c0001 | t0054 | g0264 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01884 | hp2 | a0004 | c0007 | t0048 | g0115 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01891 | hp1 | a0001 | c0001 | t0010 | g0290 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0006 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01934 | hp1 | a0003 | c0003 | t0003 | g0091 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01981 | hp1 | a0003 | c0003 | t0034 | g0100 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01993 | hp1 | a0003 | c0003 | t0003 | g0104 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01993 | hp2 | a0001 | c0001 | t0045 | g0188 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0224 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02055 | hp2 | a0003 | c0003 | t0003 | g0095 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02145 | hp1 | a0003 | c0003 | t0022 | g0078 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02145 | hp2 | a0002 | c0002 | t0005 | g0012 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02155 | hp1 | a0001 | c0001 | t0014 | g0317 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02165 | hp1 | a0001 | c0001 | t0028 | g0299 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0287 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02273 | hp1 | a0001 | c0001 | t0050 | g0156 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02273 | hp2 | a0003 | c0003 | t0003 | g0105 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02280 | hp1 | a0002 | c0002 | t0009 | g0049 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02280 | hp2 | a0003 | c0003 | t0007 | g0074 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02293 | hp2 | a0002 | c0002 | t0003 | g0041 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02451 | hp1 | a0003 | c0003 | t0004 | g0087 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02602 | hp1 | a0002 | c0002 | t0008 | g0059 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0277 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02615 | hp2 | a0002 | c0002 | t0037 | g0036 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02622 | hp1 | a0002 | c0002 | t0008 | g0060 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02622 | hp2 | a0002 | c0002 | t0049 | g0011 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0313 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02630 | hp2 | a0003 | c0003 | t0021 | g0079 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02647 | hp1 | a0002 | c0004 | t0013 | g0013 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0223 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02698 | hp1 | a0002 | c0002 | t0008 | g0058 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02698 | hp2 | a0003 | c0003 | t0003 | g0093 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02723 | hp1 | a0002 | c0002 | t0006 | g0016 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0292 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02735 | hp1 | a0003 | c0003 | t0002 | g0110 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02735 | hp2 | a0003 | c0003 | t0003 | g0088 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02738 | hp1 | a0001 | c0001 | t0023 | g0265 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02809 | hp1 | a0007 | c0006 | t0005 | g0072 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02809 | hp2 | a0002 | c0002 | t0005 | g0035 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02818 | hp1 | a0002 | c0002 | t0009 | g0001 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02818 | hp2 | a0002 | c0002 | t0008 | g0057 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02886 | hp1 | a0001 | c0009 | t0013 | g0123 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02886 | hp2 | a0002 | c0002 | t0008 | g0070 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02895 | hp1 | a0002 | c0002 | t0009 | g0046 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02897 | hp1 | a0001 | c0001 | t0020 | g0304 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02922 | hp1 | a0001 | c0001 | t0025 | g0124 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02922 | hp2 | a0002 | c0002 | t0009 | g0001 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02965 | hp1 | a0001 | c0008 | t0032 | g0307 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02965 | hp2 | a0005 | c0010 | t0025 | g0119 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02970 | hp1 | a0002 | c0002 | t0009 | g0051 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02970 | hp2 | a0002 | c0002 | t0008 | g0053 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02976 | hp1 | a0002 | c0002 | t0005 | g0056 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02976 | hp2 | a0002 | c0002 | t0005 | g0038 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03017 | hp1 | a0003 | c0003 | t0003 | g0101 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0289 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03041 | hp2 | a0001 | c0005 | t0024 | g0314 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03098 | hp1 | a0003 | c0003 | t0005 | g0116 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03130 | hp1 | a0002 | c0002 | t0009 | g0044 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0291 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03139 | hp1 | a0002 | c0002 | t0006 | g0052 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0208 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03195 | hp2 | a0002 | c0004 | t0013 | g0015 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0285 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03225 | hp1 | a0001 | c0001 | t0036 | g0269 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03225 | hp2 | a0002 | c0002 | t0009 | g0050 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03239 | hp2 | a0001 | c0001 | t0011 | g0185 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03491 | hp1 | a0002 | c0002 | t0029 | g0010 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03492 | hp2 | a0001 | c0001 | t0011 | g0158 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03516 | hp1 | a0002 | c0002 | t0008 | g0054 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03516 | hp2 | a0001 | c0001 | t0020 | g0302 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03540 | hp1 | a0001 | c0001 | t0038 | g0182 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03540 | hp2 | a0001 | c0001 | t0015 | g0205 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03579 | hp1 | a0002 | c0002 | t0009 | g0047 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03579 | hp2 | a0002 | c0002 | t0008 | g0062 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03669 | hp1 | a0003 | c0003 | t0007 | g0002 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03704 | hp2 | a0003 | c0003 | t0003 | g0102 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03710 | hp1 | a0002 | c0002 | t0039 | g0068 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03710 | hp2 | a0003 | c0003 | t0016 | g0108 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03831 | hp1 | a0003 | c0003 | t0016 | g0099 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0029 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04184 | hp1 | a0003 | c0003 | t0035 | g0092 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0113 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04199 | hp2 | a0003 | c0003 | t0016 | g0107 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04204 | hp1 | a0001 | c0001 | t0033 | g0207 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG04204 | hp2 | a0003 | c0003 | t0003 | g0094 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18522 | hp1 | a0002 | c0002 | t0008 | g0061 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18906 | hp1 | a0002 | c0002 | t0042 | g0039 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18944 | hp1 | a0001 | c0001 | t0014 | g0318 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18947 | hp1 | a0001 | c0001 | t0018 | g0139 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18948 | hp1 | a0001 | c0001 | t0044 | g0238 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18953 | hp2 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18962 | hp2 | a0001 | c0001 | t0018 | g0168 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0129 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18970 | hp2 | a0006 | c0011 | t0001 | g0176 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18974 | hp2 | a0001 | c0001 | t0026 | g0306 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18983 | hp1 | a0001 | c0001 | t0052 | g0280 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18983 | hp2 | a0001 | c0001 | t0019 | g0263 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18990 | hp1 | a0001 | c0001 | t0055 | g0127 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA18990 | hp2 | a0001 | c0001 | t0014 | g0319 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19009 | hp1 | a0001 | c0001 | t0019 | g0228 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19009 | hp2 | a0001 | c0001 | t0007 | g0125 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19011 | hp2 | a0001 | c0001 | t0027 | g0297 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0311 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19030 | hp2 | a0003 | c0003 | t0004 | g0111 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0006 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19043 | hp2 | a0001 | c0001 | t0031 | g0210 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19058 | hp2 | a0003 | c0003 | t0003 | g0089 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19060 | hp1 | a0001 | c0001 | t0018 | g0164 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19077 | hp1 | a0001 | c0001 | t0019 | g0259 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19080 | hp2 | a0001 | c0001 | t0040 | g0180 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19081 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19087 | hp2 | a0001 | c0001 | t0043 | g0251 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19089 | hp1 | a0001 | c0001 | t0046 | g0288 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19240 | hp1 | a0002 | c0002 | t0008 | g0063 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA19240 | hp2 | a0003 | c0003 | t0005 | g0082 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20129 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | ASW | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ASW | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0230 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20752 | hp2 | a0001 | c0001 | t0007 | g0133 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20805 | hp1 | a0002 | c0002 | t0017 | g0042 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0226 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20905 | hp1 | a0001 | c0001 | t0011 | g0178 | SAS | GIH | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20905 | hp2 | a0001 | c0001 | t0023 | g0248 | SAS | GIH | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0236 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG01123 | hp2 | a0003 | c0003 | t0003 | g0109 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02109 | hp1 | a0002 | c0002 | t0009 | g0048 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0213 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02486 | hp2 | a0002 | c0002 | t0022 | g0071 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02559 | hp1 | a0003 | c0003 | t0005 | g0080 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG02559 | hp2 | a0002 | c0002 | t0005 | g0034 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03471 | hp1 | a0001 | c0001 | t0020 | g0303 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG03471 | hp2 | a0001 | c0001 | t0015 | g0209 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0312 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
HG06807 | hp2 | a0003 | c0003 | t0006 | g0112 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20300 | hp1 | a0001 | c0001 | t0010 | g0286 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA20300 | hp2 | a0003 | c0003 | t0003 | g0103 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA21309 | hp1 | a0002 | c0002 | t0053 | g0055 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
NA21309 | hp2 | a0002 | c0002 | t0012 | g0033 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0047 | g0266 | REF | REF | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77343185
|
C | A | 1 | a0004 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.753G>T | p.Glu251Asp | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/6 | 794/7761 | 753/978 | 251/325 | chr14 | 77343185 | ||
chr14:77346386
|
T | A | 1 | a0005 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.290A>T | p.Asp97Val | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/6 | 331/7761 | 290/978 | 97/325 | chr14 | 77346386 | ||
chr14:77346432
|
G | A | 1 | a0006 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.244C>T | p.Arg82Trp | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/6 | 285/7761 | 244/978 | 82/325 | chr14 | 77346432 | ||
chr14:77377010
|
G | T | 1 | a0002 | 64 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(61): Show |
missense_variant | MODERATE | c.44C>A | p.Pro15His | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 85/7761 | 44/978 | 15/325 | chr14 | 77377010 | ||
chr14:77377020
|
A | G | 2 | a0003a0004 | 50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
missense_variant | MODERATE | c.34T>C | p.Ser12Pro | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 75/7761 | 34/978 | 12/325 | chr14 | 77377020 | ||
chr14:77377025
|
G | T | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.29C>A | p.Pro10Gln | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 70/7761 | 29/978 | 10/325 | chr14 | 77377025 | ||
chr14:77377041
|
G | T | 1 | a0002 | 64 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(61): Show |
missense_variant | MODERATE | c.13C>A | p.Gln5Lys | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 54/7761 | 13/978 | 5/325 | chr14 | 77377041 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77341909
|
G | A | 2 | a0001c0009a0002c0004 | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.840C>T | p.Tyr280Tyr | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 881/7761 | 840/978 | 280/325 | chr14 | 77341909 | ||
chr14:77343218
|
G | A | 1 | a0001c0005 | 2 | HG01109.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.720C>T | p.Asp240Asp | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/6 | 761/7761 | 720/978 | 240/325 | chr14 | 77343218 | ||
chr14:77343464
|
A | G | 1 | a0001c0008 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.474T>C | p.Ala158Ala | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/6 | 515/7761 | 474/978 | 158/325 | chr14 | 77343464 | ||
chr14:77343743
|
A | G | 1 | a0002c0004 | 3 | HG01081.hp2 HG02647.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.408T>C | p.Leu136Leu | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 4/6 | 449/7761 | 408/978 | 136/325 | chr14 | 77343743 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77335088
|
T | C | 20 | a0001c0001t0001a0001c0001t0011a0001c0001t0018others(17): Show | 105 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*6683A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6683 | chr14 | 77335088 | |||||
chr14:77335127
|
G | A | 2 | a0001c0009t0013a0002c0004t0013 | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6644C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6644 | chr14 | 77335127 | |||||
chr14:77335145
|
G | A | 2 | a0001c0009t0013a0002c0004t0013 | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6626C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6626 | chr14 | 77335145 | |||||
chr14:77335171
|
T | C | 1 | a0002c0002t0049 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6600A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6600 | chr14 | 77335171 | |||||
chr14:77335311
|
G | C | 19 | a0001c0001t0001a0001c0001t0011a0001c0001t0018others(16): Show | 102 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*6460C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6460 | chr14 | 77335311 | |||||
chr14:77335501
|
G | A | 1 | a0003c0003t0034 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6270C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6270 | chr14 | 77335501 | |||||
chr14:77335713
|
C | T | 1 | a0002c0002t0041 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6058G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6058 | chr14 | 77335713 | |||||
chr14:77335724
|
G | A | 1 | a0002c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6047C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6047 | chr14 | 77335724 | |||||
chr14:77335851
|
A | G | 1 | a0001c0001t0040 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5920T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 5920 | chr14 | 77335851 | |||||
chr14:77336571
|
G | A | 1 | a0001c0005t0024 | 2 | HG01109.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5200C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 5200 | chr14 | 77336571 | |||||
chr14:77336629
|
C | A | 3 | a0001c0001t0038a0002c0002t0022a0003c0003t0022 | 3 | HG02145.hp1 HG02486.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5142G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 5142 | chr14 | 77336629 | |||||
chr14:77336799
|
C | T | 1 | a0001c0001t0054 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4972G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4972 | chr14 | 77336799 | |||||
chr14:77336947
|
C | T | 1 | a0004c0007t0048 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4824G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4824 | chr14 | 77336947 | |||||
chr14:77337004
|
C | G | 1 | a0001c0001t0028 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4767G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4767 | chr14 | 77337004 | |||||
chr14:77337026
|
ATAT | A | 1 | a0001c0001t0020 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4742_*4744delATA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4742 | chr14 | 77337026 | |||||
chr14:77337183
|
C | T | 2 | a0001c0009t0013a0002c0004t0013 | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4588G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4588 | chr14 | 77337183 | |||||
chr14:77337209
|
T | C | 4 | a0001c0001t0004a0001c0001t0023a0001c0001t0033others(1): Show | 28 | HG00323.hp1 HG00621.hp2 HG00735.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4562A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4562 | chr14 | 77337209 | |||||
chr14:77337250
|
G | A | 1 | a0001c0001t0043 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4521C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4521 | chr14 | 77337250 | |||||
chr14:77337272
|
C | G | 12 | a0001c0001t0003a0001c0001t0015a0001c0001t0031others(9): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4499G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4499 | chr14 | 77337272 | |||||
chr14:77337424
|
T | G | 1 | a0001c0001t0044 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4347A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4347 | chr14 | 77337424 | |||||
chr14:77337446
|
T | C | 1 | a0001c0001t0020 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4325A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4325 | chr14 | 77337446 | |||||
chr14:77337576
|
C | T | 1 | a0003c0003t0021 | 2 | HG01167.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4195G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4195 | chr14 | 77337576 | |||||
chr14:77337680
|
G | A | 1 | a0001c0001t0045 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4091C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4091 | chr14 | 77337680 | |||||
chr14:77337771
|
C | A | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4000G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4000 | chr14 | 77337771 | |||||
chr14:77337812
|
A | G | 1 | a0001c0005t0024 | 2 | HG01109.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3959T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3959 | chr14 | 77337812 | |||||
chr14:77337967
|
C | T | 2 | a0001c0009t0013a0002c0004t0013 | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3804G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3804 | chr14 | 77337967 | |||||
chr14:77337982
|
G | A | 1 | a0003c0003t0035 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3789C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3789 | chr14 | 77337982 | |||||
chr14:77338062
|
C | T | 12 | a0001c0001t0003a0001c0001t0015a0001c0001t0031others(9): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3709G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3709 | chr14 | 77338062 | |||||
chr14:77338065
|
A | T | 1 | a0001c0001t0052 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3706T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3706 | chr14 | 77338065 | |||||
chr14:77338077
|
T | TAATGGGG others(21): Show |
1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3693_*3694insGGGA others(24): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3693 | chr14 | 77338077 | |||||
chr14:77338201
|
A | G | 1 | a0003c0003t0016 | 3 | HG03710.hp2 HG03831.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3570T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3570 | chr14 | 77338201 | |||||
chr14:77338237
|
A | G | 12 | a0001c0001t0003a0001c0001t0015a0001c0001t0031others(9): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3534T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3534 | chr14 | 77338237 | |||||
chr14:77338419
|
A | G | 1 | a0001c0001t0018 | 3 | NA18947.hp1 NA18962.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3352T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3352 | chr14 | 77338419 | |||||
chr14:77338499
|
C | T | 65 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(62): Show | 286 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*3272G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3272 | chr14 | 77338499 | |||||
chr14:77338772
|
ATATATT | A | 4 | a0001c0001t0007a0001c0001t0055a0003c0003t0007others(1): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2993_*2998delAATA others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2993 | chr14 | 77338772 | |||||
chr14:77339033
|
G | A | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(56): Show | 276 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*2738C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2738 | chr14 | 77339033 | |||||
chr14:77339482
|
G | C | 1 | a0001c0001t0054 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2289 | chr14 | 77339482 | |||||
chr14:77339641
|
G | C | 1 | a0001c0005t0024 | 2 | HG01109.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2130C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2130 | chr14 | 77339641 | |||||
chr14:77339694
|
A | C | 1 | a0002c0002t0039 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2077T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2077 | chr14 | 77339694 | |||||
chr14:77339711
|
C | T | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2060G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2060 | chr14 | 77339711 | |||||
chr14:77339712
|
T | C | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2059A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2059 | chr14 | 77339712 | |||||
chr14:77339948
|
T | C | 1 | a0002c0002t0049 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1823A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1823 | chr14 | 77339948 | |||||
chr14:77339986
|
A | ATGAAGGA others(1): Show |
64 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(61): Show | 285 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1784_*1785insCTCC others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1784 | chr14 | 77339986 | |||||
chr14:77340143
|
T | C | 16 | a0001c0001t0003a0001c0001t0015a0001c0001t0031others(13): Show | 51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1628A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1628 | chr14 | 77340143 | |||||
chr14:77340149
|
G | A | 1 | a0001c0001t0051 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1622C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1622 | chr14 | 77340149 | |||||
chr14:77340215
|
G | A | 1 | a0002c0002t0009 | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1556C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1556 | chr14 | 77340215 | |||||
chr14:77340457
|
G | A | 2 | a0001c0001t0010a0001c0001t0036 | 8 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1314C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1314 | chr14 | 77340457 | |||||
chr14:77340515
|
C | G | 4 | a0001c0001t0012a0001c0001t0038a0002c0002t0012others(1): Show | 6 | HG01891.hp2 HG02615.hp2 HG03540.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1256G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1256 | chr14 | 77340515 | |||||
chr14:77340809
|
C | T | 1 | a0002c0002t0037 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*962G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 962 | chr14 | 77340809 | |||||
chr14:77340930
|
C | CA | 7 | a0001c0001t0002a0001c0001t0014a0001c0001t0027others(4): Show | 47 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*840dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 840 | chr14 | 77340930 | |||||
chr14:77340930
|
C | CAA | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0025others(6): Show | 44 | HG00323.hp1 HG00621.hp2 HG00733.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*839_*840dupTT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 840 | chr14 | 77340930 | |||||
chr14:77340930
|
CA | C | 16 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(13): Show | 59 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*840delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 840 | chr14 | 77340930 | |||||
chr14:77340954
|
G | T | 1 | a0001c0001t0027 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 817 | chr14 | 77340954 | |||||
chr14:77341041
|
A | G | 1 | a0001c0001t0026 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 730 | chr14 | 77341041 | |||||
chr14:77341154
|
T | A | 1 | a0001c0001t0055 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 617 | chr14 | 77341154 | |||||
chr14:77341219
|
G | A | 2 | a0001c0001t0025a0005c0010t0025 | 2 | HG02922.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*552C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 552 | chr14 | 77341219 | |||||
chr14:77341467
|
T | TA | 2 | a0001c0009t0013a0002c0004t0013 | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*303dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 303 | chr14 | 77341467 | |||||
chr14:77341631
|
AAC | A | 2 | a0001c0001t0011a0001c0001t0056 | 6 | HG01071.hp2 HG01081.hp1 HG01255.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*138_*139delGT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 138 | chr14 | 77341631 | |||||
chr14:77377073
|
C | A | 1 | a0001c0001t0014 | 4 | HG00597.hp1 HG02155.hp1 NA18944.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 20 | chr14 | 77377073 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77342003
|
T | C | 1 | a0002c0002t0009g0046 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.761-15A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342003 | ||||||
chr14:77342199
|
C | G | 27 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(24): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.761-211G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342199 | ||||||
chr14:77342435
|
A | ATCTTTAC others(5): Show |
212 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(209): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.761-448_761-447ins others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342435 | ||||||
chr14:77342448
|
A | G | 1 | a0001c0001t0002g0308 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.761-460T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342448 | ||||||
chr14:77342615
|
G | A | 1 | a0001c0001t0007g0133 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.760+563C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342615 | ||||||
chr14:77342712
|
G | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.760+466C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342712 | ||||||
chr14:77342864
|
T | A | 1 | a0001c0001t0055g0127 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.760+314A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342864 | ||||||
chr14:77342877
|
A | G | 1 | a0001c0001t0027g0297 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.760+301T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342877 | ||||||
chr14:77342963
|
G | A | 1 | a0002c0002t0008g0057 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.760+215C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342963 | ||||||
chr14:77342976
|
A | G | 230 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.760+202T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342976 | ||||||
chr14:77343596
|
C | T | 104 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(101): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.454+101G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 4/5 | chr14 | 77343596 | ||||||
chr14:77343635
|
G | T | 1 | a0001c0001t0002g0237 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.454+62C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 4/5 | chr14 | 77343635 | ||||||
chr14:77343851
|
G | C | 26 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(23): Show | 26 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.328-28C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77343851 | ||||||
chr14:77344046
|
T | C | 1 | a0001c0001t0023g0265 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.328-223A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344046 | ||||||
chr14:77344176
|
C | T | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-353G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344176 | ||||||
chr14:77344200
|
A | G | 65 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(62): Show | 68 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.328-377T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344200 | ||||||
chr14:77344370
|
G | C | 104 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(101): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.328-547C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344370 | ||||||
chr14:77344434
|
T | C | 1 | a0002c0002t0008g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.328-611A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344434 | ||||||
chr14:77344545
|
G | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-722C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344545 | ||||||
chr14:77344652
|
G | A | 2 | a0001c0001t0025g0124a0005c0010t0025g0119 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-829C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344652 | ||||||
chr14:77344672
|
A | T | 69 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(66): Show | 72 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.328-849T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344672 | ||||||
chr14:77344715
|
C | T | 6 | a0003c0003t0007g0002a0003c0003t0007g0073a0003c0003t0007g0074others(3): Show | 7 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-892G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344715 | ||||||
chr14:77344792
|
CATA | C | 4 | a0001c0001t0007g0125a0001c0001t0007g0128a0001c0001t0007g0129others(1): Show | 4 | NA18953.hp2 NA18967.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-972_328-970del others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344792 | ||||||
chr14:77344991
|
C | A | 1 | a0001c0001t0005g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328-1168G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344991 | ||||||
chr14:77345137
|
G | A | 1 | a0001c0001t0010g0291 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.327+1212C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345137 | ||||||
chr14:77345276
|
C | T | 5 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+1073G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345276 | ||||||
chr14:77345374
|
G | C | 5 | a0001c0001t0001g0225a0001c0001t0001g0240a0001c0001t0001g0268others(2): Show | 5 | HG00597.hp2 HG01981.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+975C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345374 | ||||||
chr14:77345636
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.327+713C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345636 | ||||||
chr14:77345638
|
G | C | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+711C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345638 | ||||||
chr14:77345659
|
C | CA | 20 | a0001c0001t0001g0146a0001c0001t0001g0165a0001c0001t0001g0220others(17): Show | 20 | HG01175.hp2 HG01496.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+689dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | ||||||
chr14:77345659
|
C | CAA | 50 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0137others(47): Show | 50 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.327+688_327+689dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | ||||||
chr14:77345659
|
C | CAAA | 7 | a0001c0001t0001g0118a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG01433.hp2 HG02602.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+687_327+689dup others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | ||||||
chr14:77345659
|
CA | C | 81 | a0001c0001t0001g0141a0001c0001t0001g0211a0001c0001t0001g0225others(78): Show | 83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.327+689delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | ||||||
chr14:77345659
|
CAA | C | 10 | a0001c0001t0020g0303a0001c0001t0020g0304a0001c0001t0038g0182others(7): Show | 10 | HG01081.hp2 HG01109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.327+688_327+689del others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | ||||||
chr14:77345659
|
CAAAAAAA others(4): Show |
C | 63 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(60): Show | 66 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.327+679_327+689del others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | ||||||
chr14:77345708
|
A | G | 1 | a0001c0001t0028g0299 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.327+641T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345708 | ||||||
chr14:77345772
|
T | C | 203 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(200): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.327+577A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345772 | ||||||
chr14:77345870
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.327+479C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345870 | ||||||
chr14:77345923
|
C | T | 67 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(64): Show | 70 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.327+426G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345923 | ||||||
chr14:77345924
|
G | A | 1 | a0001c0001t0004g0009 | 2 | NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.327+425C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345924 | ||||||
chr14:77345947
|
C | T | 1 | a0002c0002t0001g0026 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.327+402G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345947 | ||||||
chr14:77345968
|
C | CA | 100 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0134others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.327+380dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345968 | ||||||
chr14:77345968
|
C | CAA | 28 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0149others(25): Show | 28 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.327+379_327+380dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345968 | ||||||
chr14:77345968
|
CA | C | 7 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(4): Show | 8 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+380delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345968 | ||||||
chr14:77346073
|
C | T | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+276G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77346073 | ||||||
chr14:77346199
|
A | T | 212 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(209): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.327+150T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77346199 | ||||||
chr14:77346303
|
T | G | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0226 | 3 | HG00733.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.327+46A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77346303 | ||||||
chr14:77346624
|
G | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0142others(1): Show | 4 | HG00408.hp2 NA18948.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-146C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346624 | ||||||
chr14:77346627
|
CA | C | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-150delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346627 | ||||||
chr14:77346760
|
G | GT | 166 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(163): Show | 171 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.198-283dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77346760
|
G | GTT | 54 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0149others(51): Show | 54 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.198-284_198-283dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77346760
|
G | GTTT | 8 | a0001c0001t0008g0223a0002c0002t0008g0054a0002c0002t0008g0057others(5): Show | 8 | HG02602.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-285_198-283dup others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77346760
|
GT | G | 15 | a0001c0001t0003g0203a0001c0001t0012g0006a0001c0001t0012g0201others(12): Show | 16 | HG01167.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.198-283delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77346760
|
GTT | G | 42 | a0001c0001t0003g0184a0001c0001t0003g0204a0001c0001t0003g0206others(39): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.198-284_198-283del others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77346760
|
GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0009g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198-292_198-283del others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77346760
|
GTTTTTTT others(4): Show |
G | 8 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0046others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-293_198-283del others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77346760
|
GTTTTTTT others(5): Show |
G | 2 | a0002c0002t0001g0018a0002c0002t0001g0019 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.198-294_198-283del others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | ||||||
chr14:77347081
|
C | G | 1 | a0002c0002t0022g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.198-603G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347081 | ||||||
chr14:77347346
|
G | A | 10 | a0002c0002t0008g0070a0002c0002t0009g0001a0002c0002t0009g0044others(7): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.198-868C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347346 | ||||||
chr14:77347413
|
C | T | 1 | a0002c0002t0005g0012 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.198-935G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347413 | ||||||
chr14:77347420
|
C | A | 2 | a0001c0005t0024g0314a0001c0005t0024g0315 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.198-942G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347420 | ||||||
chr14:77347556
|
C | T | 1 | a0001c0001t0054g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198-1078G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347556 | ||||||
chr14:77347557
|
G | A | 7 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0313others(4): Show | 7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-1079C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347557 | ||||||
chr14:77347658
|
G | C | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.198-1180C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347658 | ||||||
chr14:77347813
|
A | C | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-1335T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347813 | ||||||
chr14:77347868
|
A | G | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1390T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347868 | ||||||
chr14:77348230
|
C | CT | 308 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(305): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.198-1753dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348230 | ||||||
chr14:77348258
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.198-1780G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348258 | ||||||
chr14:77348445
|
G | A | 2 | a0003c0003t0003g0004a0003c0003t0003g0096 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.198-1967C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348445 | ||||||
chr14:77348468
|
C | G | 1 | a0001c0001t0006g0218 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.198-1990G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348468 | ||||||
chr14:77348518
|
C | A | 1 | a0001c0001t0008g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.198-2040G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348518 | ||||||
chr14:77348640
|
A | G | 7 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(4): Show | 7 | HG01109.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-2162T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348640 | ||||||
chr14:77348668
|
T | C | 9 | a0001c0001t0005g0285a0001c0001t0005g0312a0001c0001t0010g0277others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-2190A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348668 | ||||||
chr14:77348731
|
GTTTCT | G | 45 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(42): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.198-2258_198-2254d others(7): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348731 | ||||||
chr14:77348941
|
T | C | 1 | a0001c0001t0006g0230 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.198-2463A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348941 | ||||||
chr14:77349032
|
G | A | 1 | a0003c0003t0004g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.198-2554C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349032 | ||||||
chr14:77349106
|
C | CT | 35 | a0001c0001t0001g0136a0001c0001t0001g0153a0001c0001t0001g0155others(32): Show | 35 | HG00323.hp2 HG00423.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+2566dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | ||||||
chr14:77349106
|
C | CTT | 96 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(93): Show | 101 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.197+2565_197+2566d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | ||||||
chr14:77349106
|
C | CTTT | 58 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0003g0184others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.197+2564_197+2566d others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | ||||||
chr14:77349106
|
C | CTTTT | 24 | a0001c0001t0003g0206a0001c0001t0004g0197a0001c0001t0005g0202others(21): Show | 25 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.197+2563_197+2566d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | ||||||
chr14:77349106
|
CT | C | 9 | a0001c0001t0001g0225a0001c0001t0001g0240a0001c0001t0001g0261others(6): Show | 9 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+2566delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | ||||||
chr14:77349241
|
T | C | 67 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(64): Show | 70 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.197+2432A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349241 | ||||||
chr14:77349370
|
TGCCTCCC others(2136): Show |
T | 1 | a0001c0001t0001g0309 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.197+160_197+2302de others(1): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349370 | ||||||
chr14:77349398
|
G | A | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+2275C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349398 | ||||||
chr14:77349750
|
A | G | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+1923T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349750 | ||||||
chr14:77349857
|
G | A | 3 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.197+1816C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349857 | ||||||
chr14:77350098
|
C | T | 15 | a0001c0001t0005g0202a0001c0001t0012g0006a0001c0001t0012g0201others(12): Show | 16 | HG01167.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+1575G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350098 | ||||||
chr14:77350185
|
G | C | 4 | a0001c0001t0004g0008a0001c0001t0004g0244a0001c0001t0004g0278others(1): Show | 5 | HG00621.hp2 NA18947.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+1488C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350185 | ||||||
chr14:77350422
|
G | A | 1 | a0001c0001t0036g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197+1251C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350422 | ||||||
chr14:77350617
|
T | C | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.197+1056A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350617 | ||||||
chr14:77350977
|
C | G | 1 | a0001c0001t0002g0254 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.197+696G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350977 | ||||||
chr14:77350982
|
G | A | 1 | a0001c0001t0040g0180 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.197+691C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350982 | ||||||
chr14:77351076
|
T | C | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.197+597A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351076 | ||||||
chr14:77351214
|
C | T | 1 | a0001c0001t0005g0161 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.197+459G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351214 | ||||||
chr14:77351224
|
C | G | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+449G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351224 | ||||||
chr14:77351262
|
G | A | 2 | a0001c0001t0002g0239a0001c0001t0006g0224 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.197+411C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351262 | ||||||
chr14:77351392
|
TG | T | 317 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(314): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.197+280delC | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351392 | ||||||
chr14:77351396
|
C | T | 43 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(40): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.197+277G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351396 | ||||||
chr14:77351402
|
G | A | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+271C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351402 | ||||||
chr14:77351403
|
C | A | 2 | a0001c0005t0024g0314a0001c0005t0024g0315 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.197+270G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351403 | ||||||
chr14:77351411
|
A | AT | 75 | a0001c0001t0001g0132a0001c0001t0001g0153a0001c0001t0001g0170others(72): Show | 78 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.197+261dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | ||||||
chr14:77351411
|
A | ATT | 10 | a0001c0001t0004g0196a0001c0001t0004g0293a0001c0001t0006g0313others(7): Show | 10 | HG00735.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+260_197+261dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | ||||||
chr14:77351411
|
AT | A | 36 | a0001c0001t0005g0202a0001c0001t0007g0126a0001c0001t0007g0128others(33): Show | 38 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+261delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | ||||||
chr14:77351411
|
ATT | A | 39 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(36): Show | 41 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.197+260_197+261del others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | ||||||
chr14:77351411
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0005g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.197+252_197+261del others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | ||||||
chr14:77351411
|
ATTTTTTT others(6): Show |
A | 8 | a0001c0001t0002g0231a0001c0001t0002g0242a0001c0001t0002g0249others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+249_197+261del others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | ||||||
chr14:77351436
|
G | T | 317 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(314): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.197+237C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351436 | ||||||
chr14:77351463
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.197+210C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351463 | ||||||
chr14:77351534
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.197+139A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351534 | ||||||
chr14:77351809
|
T | C | 4 | a0001c0001t0001g0190a0001c0001t0011g0189a0001c0001t0011g0191others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-58A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77351809 | ||||||
chr14:77351898
|
C | A | 1 | a0002c0002t0053g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-147G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77351898 | ||||||
chr14:77352092
|
G | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-341C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352092 | ||||||
chr14:77352126
|
C | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG00609.hp1 NA18747.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.119-375G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352126 | ||||||
chr14:77352517
|
T | G | 1 | a0002c0002t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.119-766A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352517 | ||||||
chr14:77352537
|
G | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-786C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352537 | ||||||
chr14:77352725
|
C | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-974G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352725 | ||||||
chr14:77352904
|
G | A | 13 | a0001c0001t0008g0213a0001c0001t0008g0223a0002c0002t0008g0053others(10): Show | 13 | HG02486.hp1 HG02602.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.119-1153C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352904 | ||||||
chr14:77352922
|
TG | T | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-1172delC | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352922 | ||||||
chr14:77352926
|
T | C | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-1175A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352926 | ||||||
chr14:77353439
|
G | GT | 61 | a0001c0001t0001g0142a0001c0001t0002g0221a0001c0001t0003g0184others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-1689dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353439 | ||||||
chr14:77353439
|
GT | G | 6 | a0001c0001t0001g0163a0001c0001t0020g0302a0001c0001t0020g0303others(3): Show | 6 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-1689delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353439 | ||||||
chr14:77353644
|
T | C | 60 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(57): Show | 63 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.119-1893A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353644 | ||||||
chr14:77353669
|
A | C | 60 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(57): Show | 63 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.119-1918T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353669 | ||||||
chr14:77353692
|
C | T | 2 | a0001c0001t0004g0009a0001c0001t0004g0284 | 3 | NA18969.hp2 NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.119-1941G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353692 | ||||||
chr14:77353699
|
G | A | 2 | a0001c0005t0024g0314a0001c0005t0024g0315 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.119-1948C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353699 | ||||||
chr14:77353977
|
A | G | 1 | a0002c0002t0008g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.119-2226T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353977 | ||||||
chr14:77353997
|
C | T | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-2246G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353997 | ||||||
chr14:77354043
|
A | G | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-2292T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354043 | ||||||
chr14:77354178
|
A | G | 1 | a0001c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.119-2427T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354178 | ||||||
chr14:77354325
|
C | T | 1 | a0001c0001t0015g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.119-2574G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354325 | ||||||
chr14:77354339
|
C | T | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-2588G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354339 | ||||||
chr14:77354373
|
G | C | 1 | a0002c0002t0005g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.119-2622C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354373 | ||||||
chr14:77354763
|
G | A | 2 | a0002c0002t0029g0010a0003c0003t0003g0085 | 2 | HG00642.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.119-3012C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354763 | ||||||
chr14:77354773
|
G | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-3022C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354773 | ||||||
chr14:77354823
|
G | A | 1 | a0002c0002t0008g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.119-3072C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354823 | ||||||
chr14:77354943
|
G | T | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-3192C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354943 | ||||||
chr14:77354954
|
C | CA | 8 | a0001c0001t0001g0136a0001c0001t0001g0172a0001c0009t0013g0123others(5): Show | 8 | HG01081.hp2 HG01243.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-3204dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354954 | ||||||
chr14:77355154
|
T | TTG | 155 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.119-3405_119-3404d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355154 | ||||||
chr14:77355198
|
C | CT | 109 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(106): Show | 109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.119-3448dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355198 | ||||||
chr14:77355198
|
CT | C | 10 | a0001c0001t0010g0287a0002c0002t0009g0001a0002c0002t0009g0044others(7): Show | 11 | HG01243.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.119-3448delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355198 | ||||||
chr14:77355265
|
A | G | 228 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.119-3514T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355265 | ||||||
chr14:77355425
|
A | T | 2 | a0001c0001t0031g0210a0004c0007t0048g0115 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.119-3674T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355425 | ||||||
chr14:77355442
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-3691G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355442 | ||||||
chr14:77355448
|
G | A | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-3697C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355448 | ||||||
chr14:77355536
|
G | A | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-3785C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355536 | ||||||
chr14:77356068
|
G | A | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-4317C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356068 | ||||||
chr14:77356077
|
T | G | 1 | a0001c0001t0002g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.119-4326A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356077 | ||||||
chr14:77356269
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.119-4518A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356269 | ||||||
chr14:77356346
|
T | C | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-4595A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356346 | ||||||
chr14:77356378
|
G | A | 1 | a0002c0002t0005g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.119-4627C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356378 | ||||||
chr14:77356612
|
A | C | 48 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(45): Show | 49 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.119-4861T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356612 | ||||||
chr14:77356910
|
A | G | 27 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(24): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.119-5159T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356910 | ||||||
chr14:77357004
|
C | T | 1 | a0001c0008t0032g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.119-5253G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357004 | ||||||
chr14:77357026
|
A | C | 1 | a0001c0001t0002g0243 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.119-5275T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357026 | ||||||
chr14:77357202
|
G | C | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-5451C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357202 | ||||||
chr14:77357570
|
T | G | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-5819A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357570 | ||||||
chr14:77357722
|
C | G | 212 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(209): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.119-5971G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357722 | ||||||
chr14:77357953
|
A | G | 250 | a0001c0001t0001g0122a0001c0001t0001g0211a0001c0001t0001g0220others(247): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.119-6202T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357953 | ||||||
chr14:77358066
|
G | A | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-6315C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358066 | ||||||
chr14:77358124
|
C | CA | 68 | a0001c0001t0001g0136a0001c0001t0001g0163a0001c0001t0001g0174others(65): Show | 71 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.119-6374dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358124 | ||||||
chr14:77358124
|
C | CAA | 6 | a0001c0001t0033g0207a0002c0002t0002g0069a0002c0002t0029g0010others(3): Show | 6 | HG00741.hp1 HG02055.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-6375_119-6374d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358124 | ||||||
chr14:77358124
|
CA | C | 88 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(85): Show | 92 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.119-6374delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358124 | ||||||
chr14:77358163
|
C | T | 1 | a0001c0001t0004g0193 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.119-6412G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358163 | ||||||
chr14:77358181
|
T | TCA | 4 | a0001c0001t0005g0283a0001c0005t0024g0314a0002c0002t0005g0056others(1): Show | 4 | HG01175.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-6432_119-6431d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | ||||||
chr14:77358181
|
T | TCACACAC others(1): Show |
14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-6438_119-6431d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | ||||||
chr14:77358181
|
TCA | T | 71 | a0001c0001t0001g0179a0001c0001t0001g0305a0001c0001t0003g0184others(68): Show | 74 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.119-6432_119-6431d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | ||||||
chr14:77358181
|
TCACACAC others(1): Show |
T | 90 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(87): Show | 94 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.119-6438_119-6431d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | ||||||
chr14:77358282
|
C | G | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-6531G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358282 | ||||||
chr14:77358308
|
C | CT | 7 | a0001c0001t0001g0118a0001c0001t0001g0173a0001c0001t0001g0177others(4): Show | 7 | HG01256.hp2 HG01361.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-6558dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358308 | ||||||
chr14:77358325
|
G | A | 1 | a0001c0001t0006g0007 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.119-6574C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358325 | ||||||
chr14:77358362
|
C | T | 1 | a0002c0002t0053g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-6611G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358362 | ||||||
chr14:77358564
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.119-6813A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358564 | ||||||
chr14:77358577
|
G | A | 1 | a0003c0003t0005g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.119-6826C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358577 | ||||||
chr14:77358588
|
C | T | 61 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-6837G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358588 | ||||||
chr14:77358900
|
G | T | 5 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-7149C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358900 | ||||||
chr14:77359046
|
C | G | 1 | a0002c0002t0001g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.119-7295G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359046 | ||||||
chr14:77359232
|
C | G | 4 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0226others(1): Show | 4 | HG00733.hp2 HG01433.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7481G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359232 | ||||||
chr14:77359399
|
TAA | T | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7650_119-7649d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359399 | ||||||
chr14:77359403
|
A | C | 224 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.119-7652T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359403 | ||||||
chr14:77359508
|
T | A | 2 | a0001c0001t0004g0232a0001c0001t0004g0258 | 2 | NA18964.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.119-7757A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359508 | ||||||
chr14:77359547
|
T | G | 1 | a0001c0001t0028g0299 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.119-7796A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359547 | ||||||
chr14:77359563
|
A | G | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7812T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359563 | ||||||
chr14:77359592
|
C | T | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0226 | 3 | HG00733.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.119-7841G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359592 | ||||||
chr14:77359826
|
G | C | 1 | a0002c0002t0001g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.119-8075C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359826 | ||||||
chr14:77359899
|
G | GA | 44 | a0001c0001t0003g0184a0001c0001t0003g0203a0001c0001t0003g0204others(41): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.119-8149dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359899 | ||||||
chr14:77360025
|
A | C | 1 | a0001c0001t0002g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.119-8274T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360025 | ||||||
chr14:77360168
|
T | C | 1 | a0001c0008t0032g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.119-8417A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360168 | ||||||
chr14:77360201
|
G | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-8450C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360201 | ||||||
chr14:77360538
|
A | C | 27 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(24): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.119-8787T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360538 | ||||||
chr14:77360559
|
CT | C | 34 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(31): Show | 34 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.119-8809delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360559 | ||||||
chr14:77360973
|
C | CT | 14 | a0001c0001t0001g0136a0001c0001t0001g0281a0001c0001t0043g0251others(11): Show | 15 | HG00099.hp1 HG00673.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-9223dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360973 | ||||||
chr14:77360973
|
CT | C | 171 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(168): Show | 178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.119-9223delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360973 | ||||||
chr14:77360973
|
CTT | C | 7 | a0001c0001t0002g0275a0001c0001t0006g0276a0001c0001t0014g0317others(4): Show | 7 | HG01081.hp2 HG02155.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-9224_119-9223d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360973 | ||||||
chr14:77360994
|
T | C | 1 | a0002c0002t0017g0042 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.119-9243A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360994 | ||||||
chr14:77361054
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.119-9303C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361054 | ||||||
chr14:77361277
|
C | T | 1 | a0001c0001t0010g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-9526G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361277 | ||||||
chr14:77361410
|
T | C | 7 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0313others(4): Show | 7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-9659A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361410 | ||||||
chr14:77361681
|
T | C | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-9930A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361681 | ||||||
chr14:77361682
|
T | C | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-9931A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361682 | ||||||
chr14:77361704
|
TAG | T | 228 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.119-9955_119-9954d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361704 | ||||||
chr14:77361758
|
T | G | 1 | a0001c0001t0004g0195 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.119-10007A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361758 | ||||||
chr14:77361860
|
G | A | 8 | a0001c0001t0005g0285a0001c0001t0010g0277a0001c0001t0010g0286others(5): Show | 8 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-10109C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361860 | ||||||
chr14:77361914
|
C | T | 90 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(87): Show | 94 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.119-10163G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361914 | ||||||
chr14:77361918
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.119-10167A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361918 | ||||||
chr14:77362087
|
C | T | 4 | a0003c0003t0007g0073a0003c0003t0007g0074a0003c0003t0007g0076others(1): Show | 4 | HG01069.hp2 HG01243.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-10336G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362087 | ||||||
chr14:77362126
|
G | T | 34 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(31): Show | 34 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.119-10375C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362126 | ||||||
chr14:77362236
|
T | C | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-10485A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362236 | ||||||
chr14:77362449
|
T | C | 1 | a0001c0001t0033g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.119-10698A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362449 | ||||||
chr14:77362518
|
T | C | 4 | a0001c0001t0002g0260a0001c0001t0019g0228a0001c0001t0019g0259others(1): Show | 4 | NA18952.hp2 NA18983.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-10767A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362518 | ||||||
chr14:77362782
|
T | C | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-11031A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362782 | ||||||
chr14:77362824
|
G | T | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-11073C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362824 | ||||||
chr14:77362867
|
A | G | 83 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(80): Show | 87 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.119-11116T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362867 | ||||||
chr14:77362869
|
G | A | 3 | a0001c0001t0044g0238a0002c0002t0001g0018a0002c0002t0001g0019 | 3 | HG01515.hp1 HG01517.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.119-11118C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362869 | ||||||
chr14:77363023
|
T | C | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-11272A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363023 | ||||||
chr14:77363062
|
C | G | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-11311G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363062 | ||||||
chr14:77363130
|
A | G | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-11379T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363130 | ||||||
chr14:77363140
|
C | G | 1 | a0001c0001t0005g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.119-11389G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363140 | ||||||
chr14:77363210
|
C | T | 2 | a0002c0004t0013g0013a0002c0004t0013g0014 | 2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.119-11459G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363210 | ||||||
chr14:77363395
|
G | A | 1 | a0002c0002t0029g0010 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.119-11644C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363395 | ||||||
chr14:77363563
|
G | A | 2 | a0001c0001t0007g0128a0002c0002t0009g0051 | 2 | HG02970.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.119-11812C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363563 | ||||||
chr14:77363694
|
C | G | 5 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-11943G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363694 | ||||||
chr14:77364204
|
C | T | 27 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(24): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.119-12453G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364204 | ||||||
chr14:77364383
|
A | G | 1 | a0001c0001t0018g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.118+12553T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364383 | ||||||
chr14:77364456
|
G | C | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+12480C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364456 | ||||||
chr14:77364484
|
A | G | 2 | a0001c0005t0024g0314a0001c0005t0024g0315 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118+12452T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364484 | ||||||
chr14:77364495
|
C | T | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+12441G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364495 | ||||||
chr14:77364496
|
G | A | 27 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(24): Show | 27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.118+12440C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364496 | ||||||
chr14:77364624
|
C | T | 3 | a0001c0001t0005g0283a0001c0001t0036g0269a0002c0002t0005g0056 | 3 | HG02109.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.118+12312G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364624 | ||||||
chr14:77364638
|
C | T | 18 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(15): Show | 19 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.118+12298G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364638 | ||||||
chr14:77364686
|
C | T | 25 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(22): Show | 25 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.118+12250G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364686 | ||||||
chr14:77364922
|
C | T | 1 | a0003c0003t0005g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118+12014G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364922 | ||||||
chr14:77365006
|
C | T | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+11930G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365006 | ||||||
chr14:77365137
|
T | C | 2 | a0001c0005t0024g0314a0001c0005t0024g0315 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118+11799A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365137 | ||||||
chr14:77365189
|
T | C | 1 | a0001c0001t0010g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.118+11747A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365189 | ||||||
chr14:77365212
|
A | T | 5 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+11724T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365212 | ||||||
chr14:77365300
|
C | T | 1 | a0003c0003t0003g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118+11636G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365300 | ||||||
chr14:77365317
|
C | G | 5 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+11619G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365317 | ||||||
chr14:77365356
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118+11580T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365356 | ||||||
chr14:77365470
|
C | T | 1 | a0001c0001t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+11466G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365470 | ||||||
chr14:77365641
|
C | T | 3 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+11295G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365641 | ||||||
chr14:77365701
|
A | G | 1 | a0003c0003t0003g0101 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.118+11235T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365701 | ||||||
chr14:77365727
|
C | T | 3 | a0001c0001t0015g0205a0001c0001t0015g0208a0001c0001t0015g0209 | 3 | HG03139.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.118+11209G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365727 | ||||||
chr14:77366013
|
C | A | 1 | a0001c0001t0006g0236 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.118+10923G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366013 | ||||||
chr14:77366152
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118+10784C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366152 | ||||||
chr14:77366209
|
G | A | 1 | a0003c0003t0022g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.118+10727C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366209 | ||||||
chr14:77366306
|
A | C | 3 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+10630T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366306 | ||||||
chr14:77366325
|
C | T | 24 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(21): Show | 24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+10611G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366325 | ||||||
chr14:77366326
|
G | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+10610C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366326 | ||||||
chr14:77366352
|
C | A | 3 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+10584G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366352 | ||||||
chr14:77366540
|
A | G | 104 | a0001c0001t0001g0122a0001c0001t0001g0211a0001c0001t0001g0220others(101): Show | 108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.118+10396T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366540 | ||||||
chr14:77366739
|
C | T | 311 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(308): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.118+10197G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366739 | ||||||
chr14:77366768
|
A | T | 1 | a0001c0001t0006g0236 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.118+10168T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366768 | ||||||
chr14:77366834
|
G | A | 2 | a0001c0001t0010g0291a0001c0001t0010g0292 | 2 | HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.118+10102C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366834 | ||||||
chr14:77366846
|
A | G | 6 | a0001c0001t0001g0305a0001c0001t0026g0306a0002c0002t0001g0064others(3): Show | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+10090T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366846 | ||||||
chr14:77367032
|
G | A | 1 | a0002c0002t0001g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.118+9904C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367032 | ||||||
chr14:77367199
|
A | G | 1 | a0001c0008t0032g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+9737T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367199 | ||||||
chr14:77367233
|
C | T | 3 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0222 | 3 | HG01175.hp2 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.118+9703G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367233 | ||||||
chr14:77367240
|
T | TA | 104 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0148others(101): Show | 105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.118+9695dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367240 | ||||||
chr14:77367240
|
T | TAA | 9 | a0001c0001t0001g0175a0001c0001t0008g0213a0001c0001t0018g0139others(6): Show | 9 | HG02486.hp1 HG02602.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+9694_118+9695d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367240 | ||||||
chr14:77367240
|
TA | T | 12 | a0001c0001t0020g0303a0001c0001t0020g0304a0001c0001t0025g0124others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.118+9695delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367240 | ||||||
chr14:77367250
|
A | AAAAC | 13 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(10): Show | 14 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+9685_118+9686i others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367250 | ||||||
chr14:77367254
|
A | C | 13 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(10): Show | 14 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+9682T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367254 | ||||||
chr14:77367299
|
C | T | 1 | a0003c0003t0003g0102 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.118+9637G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367299 | ||||||
chr14:77367471
|
C | T | 7 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0313others(4): Show | 7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+9465G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367471 | ||||||
chr14:77367488
|
C | T | 1 | a0003c0003t0004g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.118+9448G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367488 | ||||||
chr14:77367593
|
GGGTCTTG others(9): Show |
G | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.118+9327_118+9342d others(18): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367593 | ||||||
chr14:77367698
|
T | TC | 5 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+9237_118+9238i others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367698 | ||||||
chr14:77367762
|
C | G | 24 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(21): Show | 24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+9174G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367762 | ||||||
chr14:77367781
|
C | T | 1 | a0002c0002t0001g0025 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.118+9155G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367781 | ||||||
chr14:77367856
|
A | G | 1 | a0003c0003t0003g0102 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.118+9080T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367856 | ||||||
chr14:77367978
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.118+8958C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367978 | ||||||
chr14:77367984
|
G | A | 24 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(21): Show | 24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+8952C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367984 | ||||||
chr14:77368057
|
T | C | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+8879A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368057 | ||||||
chr14:77368176
|
G | A | 24 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(21): Show | 24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+8760C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368176 | ||||||
chr14:77368176
|
G | T | 42 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(39): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.118+8760C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368176 | ||||||
chr14:77368277
|
A | AT | 207 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0134others(204): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.118+8658dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368277 | ||||||
chr14:77368284
|
T | A | 1 | a0001c0001t0056g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.118+8652A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368284 | ||||||
chr14:77368465
|
T | C | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+8471A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368465 | ||||||
chr14:77368467
|
A | ATTAT | 10 | a0002c0002t0008g0058a0002c0002t0009g0001a0002c0002t0009g0044others(7): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+8465_118+8468d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368467 | ||||||
chr14:77368467
|
ATTAT | A | 14 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0128others(11): Show | 15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+8465_118+8468d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368467 | ||||||
chr14:77368501
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.118+8435C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368501 | ||||||
chr14:77368589
|
G | A | 1 | a0001c0001t0054g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.118+8347C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368589 | ||||||
chr14:77368624
|
C | T | 3 | a0001c0001t0002g0242a0001c0001t0002g0282a0001c0001t0052g0280 | 3 | HG00423.hp2 HG00558.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.118+8312G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368624 | ||||||
chr14:77368678
|
T | C | 1 | a0003c0003t0003g0090 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.118+8258A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368678 | ||||||
chr14:77368718
|
G | A | 2 | a0002c0002t0005g0035a0002c0002t0005g0038 | 2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.118+8218C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368718 | ||||||
chr14:77368866
|
C | G | 1 | a0002c0002t0008g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118+8070G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368866 | ||||||
chr14:77368900
|
C | G | 1 | a0003c0003t0005g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118+8036G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368900 | ||||||
chr14:77368974
|
T | C | 1 | a0001c0001t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+7962A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368974 | ||||||
chr14:77369071
|
G | A | 1 | a0001c0001t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+7865C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369071 | ||||||
chr14:77369096
|
G | A | 171 | a0001c0001t0001g0122a0001c0001t0001g0211a0001c0001t0001g0220others(168): Show | 178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.118+7840C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369096 | ||||||
chr14:77369117
|
TTAGAA | T | 59 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(56): Show | 62 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.118+7814_118+7818d others(7): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369117 | ||||||
chr14:77369182
|
T | C | 1 | a0001c0001t0019g0263 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.118+7754A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369182 | ||||||
chr14:77369423
|
T | TG | 7 | a0001c0001t0001g0305a0001c0001t0026g0306a0001c0001t0028g0299others(4): Show | 7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+7512dupC | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369423 | ||||||
chr14:77369551
|
G | T | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+7385C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369551 | ||||||
chr14:77369770
|
G | A | 87 | a0001c0001t0001g0118a0001c0001t0001g0134a0001c0001t0001g0135others(84): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.118+7166C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369770 | ||||||
chr14:77369818
|
A | G | 1 | a0002c0002t0001g0025 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.118+7118T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369818 | ||||||
chr14:77369830
|
C | T | 9 | a0001c0001t0004g0005a0001c0001t0004g0193a0001c0001t0004g0194others(6): Show | 10 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+7106G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369830 | ||||||
chr14:77369900
|
G | A | 7 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0313others(4): Show | 7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+7036C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369900 | ||||||
chr14:77370159
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.118+6777C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370159 | ||||||
chr14:77370167
|
G | A | 4 | a0001c0009t0013g0123a0002c0004t0013g0013a0002c0004t0013g0014others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+6769C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370167 | ||||||
chr14:77370171
|
CA | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0173others(4): Show | 7 | HG01070.hp2 HG01256.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+6764delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370171 | ||||||
chr14:77370171
|
CAAAAAAA others(3): Show |
C | 207 | a0001c0001t0001g0122a0001c0001t0001g0211a0001c0001t0001g0220others(204): Show | 215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.118+6755_118+6764d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370171 | ||||||
chr14:77370171
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0241 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.118+6754_118+6764d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370171 | ||||||
chr14:77370223
|
A | G | 1 | a0001c0001t0007g0131 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.118+6713T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370223 | ||||||
chr14:77370525
|
TTG | T | 15 | a0001c0001t0001g0132a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+6409_118+6410d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370525 | ||||||
chr14:77370742
|
A | AGT | 7 | a0001c0001t0001g0143a0001c0001t0002g0301a0001c0001t0027g0297others(4): Show | 7 | HG02970.hp1 HG03130.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+6192_118+6193d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | ||||||
chr14:77370742
|
A | AGTGT | 3 | a0001c0001t0001g0170a0001c0001t0001g0177a0002c0002t0001g0017 | 3 | HG00741.hp2 HG01361.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.118+6190_118+6193d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | ||||||
chr14:77370742
|
A | AGTGTGT | 77 | a0001c0001t0001g0118a0001c0001t0001g0134a0001c0001t0001g0135others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.118+6188_118+6193d others(8): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | ||||||
chr14:77370742
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0166a0001c0001t0001g0167a0002c0002t0001g0030 | 3 | HG02132.hp1 HG02132.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.118+6186_118+6193d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | ||||||
chr14:77370742
|
AGT | A | 66 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(63): Show | 67 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.118+6192_118+6193d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | ||||||
chr14:77370742
|
AGTGT | A | 8 | a0001c0001t0002g0117a0001c0001t0006g0311a0001c0001t0025g0124others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+6190_118+6193d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | ||||||
chr14:77370742
|
AGTGTGTG others(1): Show |
A | 2 | a0003c0003t0003g0004a0003c0003t0003g0096 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.118+6186_118+6193d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | ||||||
chr14:77370767
|
A | G | 5 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+6169T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370767 | ||||||
chr14:77370817
|
T | C | 5 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0313others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+6119A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370817 | ||||||
chr14:77370864
|
G | A | 2 | a0001c0005t0024g0314a0001c0005t0024g0315 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118+6072C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370864 | ||||||
chr14:77370904
|
A | G | 1 | a0001c0001t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+6032T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370904 | ||||||
chr14:77370933
|
T | A | 110 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0134others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.118+6003A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370933 | ||||||
chr14:77371028
|
T | C | 1 | a0001c0001t0023g0265 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.118+5908A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77371028 | ||||||
chr14:77371289
|
A | G | 15 | a0001c0001t0001g0132a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+5647T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77371289 | ||||||
chr14:77371311
|
G | A | 1 | a0002c0002t0008g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118+5625C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77371311 | ||||||
chr14:77372101
|
G | A | 9 | a0001c0001t0005g0285a0001c0001t0005g0312a0001c0001t0010g0277others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+4835C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372101 | ||||||
chr14:77372121
|
C | T | 171 | a0001c0001t0001g0122a0001c0001t0001g0211a0001c0001t0001g0220others(168): Show | 178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.118+4815G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372121 | ||||||
chr14:77372163
|
A | G | 59 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(56): Show | 62 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.118+4773T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372163 | ||||||
chr14:77372338
|
C | G | 1 | a0002c0002t0001g0021 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.118+4598G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372338 | ||||||
chr14:77372413
|
C | T | 12 | a0001c0001t0005g0283a0001c0001t0005g0285a0001c0001t0005g0312others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+4523G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372413 | ||||||
chr14:77372416
|
A | G | 1 | a0003c0003t0003g0105 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.118+4520T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372416 | ||||||
chr14:77372420
|
T | C | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4516A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372420 | ||||||
chr14:77372640
|
A | C | 7 | a0001c0001t0008g0213a0002c0002t0008g0058a0002c0002t0008g0059others(4): Show | 7 | HG02486.hp1 HG02602.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+4296T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372640 | ||||||
chr14:77372714
|
T | G | 15 | a0001c0001t0001g0132a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+4222A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372714 | ||||||
chr14:77372752
|
C | T | 1 | a0001c0001t0052g0280 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.118+4184G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372752 | ||||||
chr14:77372830
|
T | G | 1 | a0007c0006t0005g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.118+4106A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372830 | ||||||
chr14:77372905
|
A | AT | 3 | a0001c0001t0011g0158a0001c0001t0011g0178a0001c0001t0028g0299 | 3 | HG02165.hp1 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.118+4030dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372905 | ||||||
chr14:77372905
|
A | ATTT | 3 | a0001c0001t0001g0187a0002c0002t0001g0032a0002c0002t0001g0067 | 3 | HG01978.hp2 HG02056.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.118+4030_118+4031i others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372905 | ||||||
chr14:77372906
|
T | TTA | 5 | a0001c0001t0001g0122a0001c0001t0001g0281a0001c0001t0052g0280others(2): Show | 5 | HG00673.hp1 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+4028_118+4029d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0268 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.118+4020_118+4029d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0002g0117a0001c0001t0004g0195 | 2 | HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.118+4014_118+4029d others(18): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
T | TTTTTTAT others(5): Show |
1 | a0001c0001t0002g0267 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.118+4029_118+4030i others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
TTA | T | 5 | a0001c0001t0001g0240a0001c0001t0002g0239a0001c0001t0006g0224others(2): Show | 5 | HG02055.hp1 HG03516.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+4028_118+4029d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
TTATATAT others(1): Show |
T | 3 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0130 | 3 | NA18946.hp1 NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.118+4022_118+4029d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
TTATATAT others(3): Show |
T | 5 | a0001c0001t0006g0236a0001c0001t0006g0310a0001c0001t0012g0201others(2): Show | 5 | HG00735.hp1 HG01123.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+4020_118+4029d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
TTATATAT others(5): Show |
T | 2 | a0001c0001t0006g0311a0002c0002t0012g0033 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.118+4018_118+4029d others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
TTATATAT others(7): Show |
T | 17 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(14): Show | 17 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.118+4016_118+4029d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
TTATATAT others(9): Show |
T | 2 | a0001c0001t0002g0215a0001c0001t0002g0216 | 2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.118+4014_118+4029d others(18): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372906
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0014g0316 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.118+4012_118+4029d others(20): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | ||||||
chr14:77372907
|
TA | T | 9 | a0001c0001t0001g0136a0001c0001t0001g0141a0001c0001t0001g0146others(6): Show | 9 | HG00609.hp2 HG01109.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+4028delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATA | T | 15 | a0001c0001t0001g0135a0001c0001t0001g0157a0001c0001t0001g0165others(12): Show | 15 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+4026_118+4028d others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATATA | T | 15 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0166others(12): Show | 15 | HG00621.hp1 HG01256.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.118+4024_118+4028d others(7): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATATATA | T | 18 | a0001c0001t0001g0118a0001c0001t0001g0134a0001c0001t0001g0138others(15): Show | 18 | HG00408.hp2 HG00558.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.118+4022_118+4028d others(9): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATATATA others(2): Show |
T | 11 | a0001c0001t0001g0137a0001c0001t0001g0149a0001c0001t0001g0150others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+4020_118+4028d others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATATATA others(4): Show |
T | 10 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0153others(7): Show | 10 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4018_118+4028d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATATATA others(16): Show |
T | 1 | a0002c0002t0001g0019 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.118+4006_118+4028d others(25): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATATATA others(18): Show |
T | 1 | a0002c0002t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118+4004_118+4028d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372907
|
TATATATA others(20): Show |
T | 1 | a0002c0002t0022g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118+4002_118+4028d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | ||||||
chr14:77372908
|
A | T | 21 | a0001c0001t0001g0132a0001c0001t0002g0221a0001c0001t0002g0237others(18): Show | 22 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+4028T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372908 | ||||||
chr14:77372910
|
A | T | 10 | a0001c0001t0001g0136a0001c0001t0001g0141a0001c0001t0001g0146others(7): Show | 10 | HG00609.hp2 HG01109.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4026T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372910 | ||||||
chr14:77372912
|
A | T | 14 | a0001c0001t0001g0135a0001c0001t0001g0157a0001c0001t0001g0165others(11): Show | 14 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+4024T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372912 | ||||||
chr14:77372914
|
A | T | 13 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0173others(10): Show | 13 | HG00621.hp1 HG01256.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.118+4022T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372914 | ||||||
chr14:77372916
|
A | T | 17 | a0001c0001t0001g0118a0001c0001t0001g0134a0001c0001t0001g0138others(14): Show | 17 | HG00408.hp2 HG00558.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.118+4020T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372916 | ||||||
chr14:77372918
|
A | T | 10 | a0001c0001t0001g0137a0001c0001t0001g0149a0001c0001t0001g0150others(7): Show | 10 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4018T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372918 | ||||||
chr14:77372920
|
A | T | 9 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0159others(6): Show | 9 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+4016T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372920 | ||||||
chr14:77372924
|
ATATATAT others(22): Show |
A | 1 | a0003c0003t0021g0081 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.118+3983_118+4011d others(31): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372924 | ||||||
chr14:77372926
|
ATATATAT others(20): Show |
A | 3 | a0002c0002t0053g0055a0003c0003t0005g0116a0003c0003t0021g0079 | 3 | HG02630.hp2 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.118+3983_118+4009d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372926 | ||||||
chr14:77372928
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0036g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+3983_118+4007d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372928 | ||||||
chr14:77372930
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0010g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.118+3982_118+4005d others(26): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372930 | ||||||
chr14:77372930
|
ATATATAT others(18): Show |
A | 2 | a0001c0001t0005g0283a0002c0002t0005g0056 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.118+3981_118+4005d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372930 | ||||||
chr14:77372930
|
ATATATAT others(21): Show |
A | 1 | a0002c0002t0008g0057 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.118+3978_118+4005d others(30): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372930 | ||||||
chr14:77372931
|
TATATATA others(14): Show |
T | 1 | a0001c0001t0004g0229 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.118+3984_118+4004d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372931 | ||||||
chr14:77372932
|
A | T | 1 | a0002c0002t0001g0019 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.118+4004T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0002g0270 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.118+3983_118+4003d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(15): Show |
A | 2 | a0003c0003t0003g0004a0003c0003t0003g0096 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.118+3982_118+4003d others(24): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(17): Show |
A | 4 | a0001c0001t0005g0285a0001c0001t0005g0312a0001c0001t0010g0286others(1): Show | 4 | HG02257.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+3980_118+4003d others(26): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0010g0289 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.118+3979_118+4003d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(23): Show |
A | 1 | a0002c0002t0008g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.118+3974_118+4003d others(32): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(24): Show |
A | 1 | a0002c0002t0008g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118+3973_118+4003d others(33): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(25): Show |
A | 3 | a0001c0001t0008g0213a0002c0002t0008g0060a0002c0002t0008g0061 | 3 | HG02486.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.118+3972_118+4003d others(34): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372932
|
ATATATAT others(26): Show |
A | 1 | a0002c0002t0008g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.118+3971_118+4003d others(35): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | ||||||
chr14:77372934
|
A | T | 1 | a0002c0002t0001g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118+4002T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0014g0318 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.118+3983_118+4001d others(21): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0014g0319 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.118+3982_118+4001d others(22): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(14): Show |
A | 5 | a0002c0002t0009g0044a0002c0002t0009g0045a0002c0002t0009g0046others(2): Show | 5 | HG01243.hp2 HG02109.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+3981_118+4001d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(15): Show |
A | 1 | a0002c0002t0009g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.118+3980_118+4001d others(24): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0010g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.118+3979_118+4001d others(25): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0010g0292 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.118+3978_118+4001d others(26): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(20): Show |
A | 1 | a0007c0006t0005g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.118+3975_118+4001d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372934
|
ATATATAT others(23): Show |
A | 1 | a0002c0002t0008g0062 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.118+3972_118+4001d others(32): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | ||||||
chr14:77372935
|
TATATATA others(8): Show |
T | 3 | a0001c0001t0002g0222a0002c0002t0005g0034a0005c0010t0025g0119 | 3 | HG01175.hp2 HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.118+3986_118+4000d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372935 | ||||||
chr14:77372936
|
A | T | 1 | a0002c0002t0022g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118+4000T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | ||||||
chr14:77372936
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0025g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.118+3983_118+3999d others(19): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | ||||||
chr14:77372936
|
ATATATAT others(12): Show |
A | 1 | a0003c0003t0005g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118+3981_118+3999d others(21): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | ||||||
chr14:77372936
|
ATATATAT others(14): Show |
A | 3 | a0001c0001t0010g0291a0002c0002t0009g0050a0002c0002t0009g0051 | 3 | HG02970.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.118+3979_118+3999d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | ||||||
chr14:77372937
|
TATATATA others(8): Show |
T | 1 | a0003c0003t0004g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118+3984_118+3998d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372937 | ||||||
chr14:77372938
|
ATATATAT others(8): Show |
A | 4 | a0001c0001t0015g0208a0002c0002t0005g0038a0002c0002t0029g0010others(1): Show | 4 | HG02698.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3983_118+3997d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372938 | ||||||
chr14:77372938
|
ATATATAT others(12): Show |
A | 1 | a0002c0002t0009g0001 | 2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.118+3979_118+3997d others(21): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372938 | ||||||
chr14:77372938
|
ATATATAT others(20): Show |
A | 1 | a0002c0002t0008g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.118+3971_118+3997d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372938 | ||||||
chr14:77372939
|
TATATATA others(6): Show |
T | 1 | a0002c0002t0037g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.118+3984_118+3996d others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372939 | ||||||
chr14:77372940
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0015g0209a0003c0003t0003g0094 | 2 | HG03471.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.118+3983_118+3995d others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372940 | ||||||
chr14:77372940
|
ATATATAT others(7): Show |
A | 2 | a0003c0003t0003g0097a0003c0003t0003g0098 | 2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.118+3982_118+3995d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372940 | ||||||
chr14:77372940
|
ATATATAT others(8): Show |
A | 1 | a0003c0003t0034g0100 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.118+3981_118+3995d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372940 | ||||||
chr14:77372942
|
ATATATAT others(4): Show |
A | 2 | a0003c0003t0003g0003a0003c0003t0003g0095 | 3 | HG00140.hp2 HG00738.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.118+3983_118+3993d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | ||||||
chr14:77372942
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0005g0202a0002c0002t0006g0016 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.118+3982_118+3993d others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | ||||||
chr14:77372942
|
ATATATAT others(6): Show |
A | 1 | a0003c0003t0003g0101 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.118+3981_118+3993d others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | ||||||
chr14:77372942
|
ATATATAT others(7): Show |
A | 4 | a0003c0003t0003g0102a0003c0003t0003g0103a0003c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG01993.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3980_118+3993d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | ||||||
chr14:77372943
|
TATATATA others(2): Show |
T | 2 | a0001c0001t0012g0006a0002c0002t0017g0040 | 3 | HG00642.hp2 HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.118+3984_118+3992d others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372943 | ||||||
chr14:77372944
|
ATATATAT others(2): Show |
A | 6 | a0002c0002t0042g0039a0003c0003t0007g0002a0003c0003t0007g0074others(3): Show | 7 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3983_118+3991d others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | ||||||
chr14:77372944
|
ATATATAT others(3): Show |
A | 1 | a0003c0003t0016g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.118+3982_118+3991d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | ||||||
chr14:77372944
|
ATATATAT others(5): Show |
A | 2 | a0003c0003t0003g0105a0003c0003t0003g0106 | 2 | HG01258.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.118+3980_118+3991d others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | ||||||
chr14:77372944
|
ATATATAT others(7): Show |
A | 1 | a0003c0003t0003g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.118+3978_118+3991d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | ||||||
chr14:77372946
|
ATATATAT others(4): Show |
A | 2 | a0003c0003t0016g0107a0003c0003t0016g0108 | 2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.118+3979_118+3989d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372946 | ||||||
chr14:77372947
|
TA | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+3988delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372947 | ||||||
chr14:77372948
|
A | T | 7 | a0001c0001t0020g0302a0001c0001t0020g0303a0002c0002t0001g0017others(4): Show | 7 | HG00741.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3988T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372948 | ||||||
chr14:77372949
|
TA | T | 10 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 10 | HG00099.hp1 HG01070.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+3986delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372949 | ||||||
chr14:77372950
|
A | ATT | 3 | a0001c0001t0001g0220a0001c0001t0006g0218a0001c0001t0006g0219 | 3 | HG00733.hp2 HG01433.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.118+3985_118+3986i others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372950 | ||||||
chr14:77372950
|
A | T | 28 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(25): Show | 28 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.118+3986T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372950 | ||||||
chr14:77372951
|
TA | T | 13 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(10): Show | 14 | HG01069.hp1 HG02132.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+3984delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372951 | ||||||
chr14:77372952
|
A | ATAT | 7 | a0001c0001t0002g0212a0001c0001t0002g0231a0001c0001t0002g0234others(4): Show | 7 | HG00544.hp1 HG02165.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3983_118+3984i others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | ||||||
chr14:77372952
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0002g0221 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.118+3983_118+3984i others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | ||||||
chr14:77372952
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0019g0228a0001c0001t0027g0297 | 2 | NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.118+3983_118+3984i others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | ||||||
chr14:77372952
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0002g0214a0003c0003t0002g0110 | 2 | HG02056.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.118+3983_118+3984i others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | ||||||
chr14:77372952
|
A | T | 81 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(78): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.118+3984T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | ||||||
chr14:77372952
|
AT | A | 7 | a0001c0001t0001g0118a0001c0001t0001g0179a0001c0001t0001g0181others(4): Show | 7 | HG00735.hp2 HG01433.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+3983delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | ||||||
chr14:77372952
|
ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0001g0190a0001c0001t0011g0189a0001c0001t0011g0191others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+3976_118+3983d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | ||||||
chr14:77372953
|
T | TA | 7 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0002g0272others(4): Show | 8 | HG00673.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.118+3982_118+3983i others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372953 | ||||||
chr14:77372953
|
T | TATA | 3 | a0001c0001t0001g0309a0001c0001t0002g0274a0001c0001t0002g0275 | 3 | NA18963.hp2 NA18970.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.118+3982_118+3983i others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372953 | ||||||
chr14:77372953
|
T | TATATATA others(4): Show |
1 | a0001c0001t0006g0276 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.118+3982_118+3983i others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372953 | ||||||
chr14:77372954
|
T | A | 11 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0187others(8): Show | 11 | HG00673.hp1 HG01978.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+3982A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372954 | ||||||
chr14:77372955
|
T | A | 6 | a0001c0001t0002g0282a0001c0001t0004g0196a0001c0001t0004g0197others(3): Show | 6 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+3981A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372955 | ||||||
chr14:77372956
|
T | A | 1 | a0002c0004t0013g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118+3980A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372956 | ||||||
chr14:77372957
|
T | A | 6 | a0001c0001t0004g0196a0001c0001t0004g0197a0001c0001t0004g0198others(3): Show | 6 | HG00323.hp1 HG00735.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+3979A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372957 | ||||||
chr14:77372958
|
T | A | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3978A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372958 | ||||||
chr14:77372959
|
T | A | 2 | a0001c0001t0004g0199a0001c0001t0004g0200 | 2 | HG00323.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.118+3977A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372959 | ||||||
chr14:77372960
|
T | A | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3976A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372960 | ||||||
chr14:77372962
|
T | A | 3 | a0001c0001t0002g0295a0001c0001t0002g0296a0004c0007t0048g0115 | 3 | HG01884.hp2 NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3974A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372962 | ||||||
chr14:77372963
|
T | A | 2 | a0001c0001t0001g0294a0001c0001t0004g0293 | 2 | NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.118+3973A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372963 | ||||||
chr14:77372964
|
T | A | 3 | a0001c0001t0002g0295a0001c0001t0002g0296a0004c0007t0048g0115 | 3 | HG01884.hp2 NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3972A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372964 | ||||||
chr14:77372966
|
T | A | 3 | a0001c0001t0002g0295a0001c0001t0002g0296a0004c0007t0048g0115 | 3 | HG01884.hp2 NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3970A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372966 | ||||||
chr14:77372968
|
T | A | 1 | a0001c0001t0002g0296 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.118+3968A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372968 | ||||||
chr14:77372991
|
C | T | 59 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(56): Show | 62 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.118+3945G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372991 | ||||||
chr14:77373004
|
C | T | 86 | a0001c0001t0001g0118a0001c0001t0001g0134a0001c0001t0001g0135others(83): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.118+3932G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373004 | ||||||
chr14:77373005
|
G | A | 15 | a0001c0001t0001g0132a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+3931C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373005 | ||||||
chr14:77373047
|
C | G | 1 | a0001c0008t0032g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+3889G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373047 | ||||||
chr14:77373096
|
G | C | 1 | a0001c0008t0032g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+3840C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373096 | ||||||
chr14:77373170
|
A | G | 1 | a0003c0003t0021g0079 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.118+3766T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373170 | ||||||
chr14:77373302
|
T | TA | 15 | a0001c0001t0001g0132a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+3633dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373302 | ||||||
chr14:77373307
|
A | C | 1 | a0001c0001t0008g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118+3629T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373307 | ||||||
chr14:77373313
|
C | A | 3 | a0001c0001t0006g0310a0001c0001t0006g0313a0002c0002t0006g0016 | 3 | HG02630.hp1 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.118+3623G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373313 | ||||||
chr14:77373314
|
A | G | 9 | a0002c0002t0009g0001a0002c0002t0009g0044a0002c0002t0009g0045others(6): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+3622T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373314 | ||||||
chr14:77373393
|
A | C | 2 | a0001c0008t0032g0307a0002c0002t0001g0017 | 2 | HG00741.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.118+3543T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373393 | ||||||
chr14:77373706
|
T | G | 2 | a0001c0001t0002g0301a0001c0001t0027g0297 | 2 | NA18989.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.118+3230A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373706 | ||||||
chr14:77373713
|
T | C | 110 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0134others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.118+3223A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373713 | ||||||
chr14:77373756
|
G | A | 42 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(39): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.118+3180C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373756 | ||||||
chr14:77374024
|
G | A | 1 | a0001c0001t0031g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.118+2912C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374024 | ||||||
chr14:77374615
|
A | G | 1 | a0001c0001t0006g0310 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.118+2321T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374615 | ||||||
chr14:77374751
|
C | T | 2 | a0002c0002t0005g0012a0002c0002t0049g0011 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.118+2185G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374751 | ||||||
chr14:77374824
|
G | A | 90 | a0001c0001t0001g0118a0001c0001t0001g0134a0001c0001t0001g0135others(87): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.118+2112C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374824 | ||||||
chr14:77374936
|
A | T | 1 | a0001c0001t0002g0212 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.118+2000T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374936 | ||||||
chr14:77374956
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.118+1980G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374956 | ||||||
chr14:77375015
|
C | T | 62 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0206others(59): Show | 65 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.118+1921G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375015 | ||||||
chr14:77375194
|
T | C | 1 | a0003c0003t0003g0114 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.118+1742A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375194 | ||||||
chr14:77375245
|
C | T | 9 | a0001c0001t0004g0005a0001c0001t0004g0193a0001c0001t0004g0194others(6): Show | 10 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+1691G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375245 | ||||||
chr14:77375406
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.118+1530C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375406 | ||||||
chr14:77375451
|
G | A | 1 | a0001c0001t0002g0301 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.118+1485C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375451 | ||||||
chr14:77375705
|
A | G | 117 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(114): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.118+1231T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375705 | ||||||
chr14:77375733
|
T | C | 3 | a0001c0001t0020g0302a0001c0001t0020g0303a0001c0001t0020g0304 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+1203A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375733 | ||||||
chr14:77375802
|
T | C | 6 | a0001c0001t0001g0305a0001c0001t0026g0306a0002c0002t0001g0064others(3): Show | 6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+1134A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375802 | ||||||
chr14:77376026
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.118+910G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376026 | ||||||
chr14:77376103
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118+833T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376103 | ||||||
chr14:77376131
|
T | C | 1 | a0002c0002t0039g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.118+805A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376131 | ||||||
chr14:77376314
|
T | C | 2 | a0001c0008t0032g0307a0002c0002t0002g0069 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118+622A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376314 | ||||||
chr14:77376552
|
G | A | 1 | a0001c0001t0002g0308 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.118+384C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376552 | ||||||
chr14:77376557
|
G | A | 2 | a0003c0003t0005g0116a0004c0007t0048g0115 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.118+379C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376557 | ||||||
chr14:77376561
|
G | A | 1 | a0002c0002t0008g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.118+375C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376561 | ||||||
chr14:77376823
|
G | A | 1 | a0002c0002t0022g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118+113C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376823 | ||||||
chr14:77376877
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.118+59C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376877 | ||||||
chr14:77376879
|
G | A | 7 | a0001c0001t0005g0312a0001c0001t0006g0310a0001c0001t0006g0311others(4): Show | 7 | HG01109.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+57C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376879 |