geneid | 203197 |
---|---|
ensemblid | ENSG00000157693.15 |
hgncid | 24513 |
symbol | TMEM268 |
name | transmembrane protein 268 |
refseq_nuc | NM_153045.4 |
refseq_prot | NP_694590.2 |
ensembl_nuc | ENST00000288502.9 |
ensembl_prot | ENSP00000288502.4 |
mane_status | MANE Select |
chr | chr9 |
start | 114611291 |
end | 114646422 |
strand | + |
ver | v1.2 |
region | chr9:114611291-114646422 |
region5000 | chr9:114606291-114651422 |
regionname0 | TMEM268_chr9_114611291_114646422 |
regionname5000 | TMEM268_chr9_114606291_114651422 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 342 | 396 | 85 | 75 | 178 | 14 | 42 | 143 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0002 | 0/0 | 342 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0003 | 0/0 | 342 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0004 | 0/0 | 342 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0005 | 0/0 | 342 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0006 | 0/0 | 342 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0007 | 0/0 | 342 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0008 | 0/0 | 342 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1029 | 363 | 83 | 74 | 150 | 14 | 40 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0002 | 0/0 | 1029 | 23 | 0 | 0 | 21 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0003 | 0/0 | 1029 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0004 | 0/0 | 1029 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0005 | 0/0 | 1029 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0006 | 0/0 | 1029 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0007 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0008 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0009 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0010 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0011 | 0/0 | 1029 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0012 | 0/0 | 1029 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0013 | 0/0 | 1029 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0014 | 0/0 | 1029 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
c0015 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3465 | 122 | 32 | 29 | 46 | 5 | 10 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0002 | 1/1 | 3462 | 79 | 7 | 14 | 41 | 4 | 11 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0003 | 0/0 | 3465 | 34 | 1 | 2 | 24 | 0 | 7 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0004 | 0/0 | 3475 | 27 | 2 | 1 | 23 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0005 | 0/0 | 3469 | 17 | 0 | 0 | 17 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0006 | 0/0 | 3462 | 11 | 10 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0007 | 0/0 | 3464 | 11 | 2 | 4 | 1 | 2 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0008 | 0/0 | 3469 | 10 | 0 | 8 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0009 | 0/0 | 3463 | 9 | 5 | 3 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0010 | 0/0 | 3468 | 9 | 1 | 2 | 6 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0011 | 0/0 | 3453 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0012 | 0/0 | 3469 | 5 | 0 | 0 | 0 | 0 | 5 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0013 | 0/0 | 3462 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0014 | 0/0 | 3468 | 4 | 0 | 0 | 3 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0015 | 0/0 | 3462 | 4 | 0 | 3 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0016 | 0/0 | 3465 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0017 | 0/0 | 3462 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0018 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0019 | 0/0 | 3471 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0020 | 0/0 | 3468 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0021 | 0/0 | 3453 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0022 | 0/0 | 3463 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0023 | 0/0 | 3474 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0024 | 0/0 | 3465 | 2 | 1 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0025 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0026 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0027 | 0/0 | 3469 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0028 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0029 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0030 | 0/0 | 3468 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0031 | 0/0 | 3468 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0032 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0033 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0034 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0035 | 0/0 | 3463 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0036 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0037 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0038 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0039 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0040 | 0/0 | 3474 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0041 | 0/0 | 3467 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0042 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0043 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0044 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0045 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0046 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0047 | 0/0 | 3468 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0048 | 0/0 | 3469 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0049 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0050 | 0/0 | 3464 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
t0051 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 39 | 11 | 6 | 20 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0002 | 0/0 | 13 | 0 | 1 | 10 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0007 | 0/0 | 6 | 0 | 3 | 1 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0009 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0010 | 0/0 | 5 | 2 | 1 | 1 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0012 | 1/0 | 4 | 0 | 1 | 0 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0037 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1029 | 363 | 83 | 74 | 150 | 14 | 40 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0002 | 0/0 | 1029 | 23 | 0 | 0 | 21 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0003 | 0/0 | 1029 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0005 | 0/0 | 1029 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0007 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0009 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0012 | 0/0 | 1029 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0015 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0002c0004 | 0/0 | 1029 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0003c0006 | 0/0 | 1029 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0004c0014 | 0/0 | 1029 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0005c0013 | 0/0 | 1029 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0006c0011 | 0/0 | 1029 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0007c0008 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0008c0010 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4493 | 118 | 30 | 28 | 45 | 5 | 10 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0002 | 1/1 | 4490 | 70 | 7 | 14 | 34 | 4 | 9 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0003 | 0/0 | 4493 | 33 | 1 | 1 | 24 | 0 | 7 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0004 | 0/0 | 4503 | 27 | 2 | 1 | 23 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0006 | 0/0 | 4490 | 11 | 10 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0007 | 0/0 | 4492 | 11 | 2 | 4 | 1 | 2 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0008 | 0/0 | 4497 | 10 | 0 | 8 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0009 | 0/0 | 4491 | 9 | 5 | 3 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0010 | 0/0 | 4496 | 9 | 1 | 2 | 6 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0011 | 0/0 | 4481 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0012 | 0/0 | 4497 | 5 | 0 | 0 | 0 | 0 | 5 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0013 | 0/0 | 4490 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0015 | 0/0 | 4490 | 4 | 0 | 3 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0016 | 0/0 | 4493 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0017 | 0/0 | 4490 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0018 | 0/0 | 4493 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0019 | 0/0 | 4499 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0020 | 0/0 | 4496 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0022 | 0/0 | 4491 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0023 | 0/0 | 4502 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0024 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0025 | 0/0 | 4493 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0026 | 0/0 | 4493 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0027 | 0/0 | 4497 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0028 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0030 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0031 | 0/0 | 4496 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0032 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0034 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0035 | 0/0 | 4491 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0036 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0037 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0038 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0039 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0040 | 0/0 | 4502 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0041 | 0/0 | 4495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0042 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0043 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0044 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0045 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0046 | 0/0 | 4493 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0047 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0048 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0049 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0050 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0001t0051 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0002t0005 | 0/0 | 4497 | 17 | 0 | 0 | 17 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0002t0014 | 0/0 | 4496 | 4 | 0 | 0 | 3 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0002t0024 | 0/0 | 4493 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0002t0033 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0003t0002 | 0/0 | 4490 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0005t0002 | 0/0 | 4490 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0007t0023 | 0/0 | 4502 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0009t0001 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0012t0001 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0001c0015t0001 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0002c0004t0013 | 0/0 | 4490 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0002c0004t0029 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0003c0006t0021 | 0/0 | 4481 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0004c0014t0002 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0005c0013t0003 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0006c0011t0002 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0007c0008t0002 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
a0008c0010t0001 | 0/0 | 4493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | copy fasta | chr9 | 114606291 | 114651422 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 32 | 9 | 5 | 16 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0010 | 0/0 | 5 | 2 | 1 | 1 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0002 | 0/0 | 11 | 0 | 1 | 8 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0007 | 0/0 | 6 | 0 | 3 | 1 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0012 | 1/0 | 4 | 0 | 1 | 0 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0037 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0009 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0001 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0011g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0011g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0012g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0012g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0012g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0013g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0015g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0015g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0015g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0015g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0017g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0017g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0017g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0018g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0018g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0018g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0019g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0020g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0022g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0022g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0023g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0024g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0025g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0025g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0026g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0026g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0027g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0027g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0028g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0030g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0031g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0032g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0034g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0035g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0036g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0037g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0038g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0039g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0040g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0041g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0042g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0043g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0044g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0045g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0046g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0047g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0048g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0049g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0050g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0051g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0014g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0014g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0014g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0014g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0024g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0033g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0003t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0005t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0005t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0007t0023g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0009t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0012t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0015t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0002c0004t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0002c0004t0013g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0002c0004t0029g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0003c0006t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0003c0006t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0004c0014t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0005c0013t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0006c0011t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0007c0008t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0008c0010t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00140 | hp1 | a0001 | c0001 | t0019 | g0041 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00408 | hp2 | a0001 | c0001 | t0011 | g0013 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00423 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0009 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00544 | hp1 | a0007 | c0008 | t0002 | g0008 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0216 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00733 | hp1 | a0001 | c0001 | t0009 | g0098 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00738 | hp2 | a0001 | c0001 | t0043 | g0195 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01074 | hp1 | a0001 | c0001 | t0015 | g0202 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0217 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0100 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0051 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01168 | hp2 | a0001 | c0001 | t0007 | g0218 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0052 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01243 | hp1 | a0001 | c0001 | t0035 | g0026 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01243 | hp2 | a0001 | c0001 | t0028 | g0179 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0149 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0207 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01257 | hp2 | a0001 | c0001 | t0040 | g0057 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01258 | hp1 | a0001 | c0001 | t0015 | g0208 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0097 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0221 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01515 | hp2 | a0001 | c0001 | t0046 | g0132 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01517 | hp2 | a0001 | c0001 | t0007 | g0039 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01884 | hp1 | a0001 | c0001 | t0027 | g0049 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01891 | hp1 | a0001 | c0001 | t0017 | g0040 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01891 | hp2 | a0001 | c0001 | t0016 | g0201 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0048 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01928 | hp2 | a0001 | c0001 | t0044 | g0035 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01975 | hp2 | a0001 | c0001 | t0023 | g0056 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01978 | hp1 | a0001 | c0001 | t0019 | g0041 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01978 | hp2 | a0001 | c0001 | t0042 | g0122 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01981 | hp1 | a0001 | c0001 | t0041 | g0176 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01981 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02004 | hp1 | a0005 | c0013 | t0003 | g0167 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02004 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02027 | hp2 | a0001 | c0002 | t0014 | g0242 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02056 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02080 | hp1 | a0001 | c0001 | t0007 | g0219 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02132 | hp1 | a0001 | c0001 | t0030 | g0238 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02148 | hp1 | a0001 | c0012 | t0001 | g0123 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02155 | hp1 | a0001 | c0001 | t0010 | g0146 | EAS | CDX | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02155 | hp2 | a0001 | c0002 | t0014 | g0240 | EAS | CDX | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02257 | hp1 | a0001 | c0001 | t0026 | g0140 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0046 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0183 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02273 | hp2 | a0001 | c0001 | t0008 | g0050 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02280 | hp1 | a0001 | c0001 | t0025 | g0159 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0047 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0223 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02523 | hp2 | a0001 | c0001 | t0022 | g0092 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02602 | hp1 | a0001 | c0001 | t0031 | g0246 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02602 | hp2 | a0001 | c0001 | t0007 | g0220 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0233 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02622 | hp2 | a0001 | c0001 | t0018 | g0227 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0137 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0096 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02647 | hp2 | a0002 | c0004 | t0013 | g0232 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02698 | hp2 | a0001 | c0001 | t0012 | g0239 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02717 | hp1 | a0001 | c0001 | t0013 | g0211 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02735 | hp1 | a0001 | c0001 | t0009 | g0086 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02738 | hp1 | a0001 | c0001 | t0036 | g0106 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02809 | hp2 | a0001 | c0001 | t0017 | g0040 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0224 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02886 | hp2 | a0001 | c0001 | t0025 | g0114 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0225 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0257 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02896 | hp1 | a0001 | c0001 | t0027 | g0053 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0226 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03017 | hp1 | a0001 | c0002 | t0024 | g0121 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03098 | hp1 | a0002 | c0004 | t0013 | g0230 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03098 | hp2 | a0001 | c0009 | t0001 | g0001 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03130 | hp1 | a0003 | c0006 | t0021 | g0172 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03139 | hp2 | a0001 | c0001 | t0049 | g0212 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0026 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0101 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0213 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03453 | hp2 | a0001 | c0001 | t0048 | g0259 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03491 | hp2 | a0001 | c0001 | t0012 | g0043 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0043 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0248 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03654 | hp1 | a0001 | c0001 | t0008 | g0009 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03654 | hp2 | a0004 | c0014 | t0002 | g0255 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03669 | hp1 | a0001 | c0001 | t0012 | g0042 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03688 | hp2 | a0001 | c0001 | t0007 | g0222 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03704 | hp1 | a0001 | c0001 | t0051 | g0215 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03942 | hp1 | a0001 | c0001 | t0050 | g0214 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0042 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04199 | hp2 | a0006 | c0011 | t0002 | g0095 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0063 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0228 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18612 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18906 | hp1 | a0001 | c0001 | t0038 | g0102 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18951 | hp2 | a0001 | c0002 | t0005 | g0044 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18956 | hp2 | a0001 | c0001 | t0022 | g0077 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18964 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18965 | hp1 | a0001 | c0005 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18966 | hp1 | a0001 | c0005 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18979 | hp2 | a0001 | c0001 | t0010 | g0196 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18982 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18987 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18988 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18989 | hp1 | a0001 | c0001 | t0032 | g0245 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18994 | hp2 | a0001 | c0002 | t0033 | g0243 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18995 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18995 | hp2 | a0001 | c0001 | t0010 | g0168 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18997 | hp1 | a0001 | c0001 | t0034 | g0200 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18997 | hp2 | a0001 | c0001 | t0037 | g0254 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18999 | hp2 | a0001 | c0001 | t0010 | g0163 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19001 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19002 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19003 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19005 | hp1 | a0001 | c0001 | t0011 | g0133 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19009 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19010 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19011 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0103 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19055 | hp2 | a0001 | c0007 | t0023 | g0071 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19056 | hp2 | a0001 | c0002 | t0005 | g0044 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19057 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19057 | hp2 | a0008 | c0010 | t0001 | g0139 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19058 | hp1 | a0001 | c0001 | t0011 | g0155 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19058 | hp2 | a0001 | c0002 | t0005 | g0236 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19060 | hp2 | a0001 | c0002 | t0005 | g0244 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19063 | hp2 | a0001 | c0002 | t0005 | g0247 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19064 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19068 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19079 | hp1 | a0001 | c0005 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19081 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19084 | hp1 | a0001 | c0001 | t0039 | g0085 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19085 | hp1 | a0001 | c0001 | t0047 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19085 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19086 | hp1 | a0001 | c0002 | t0005 | g0235 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19091 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | ASW | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20129 | hp2 | a0002 | c0004 | t0029 | g0231 | AFR | ASW | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20805 | hp1 | a0001 | c0001 | t0015 | g0209 | EUR | TSI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | TSI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20905 | hp1 | a0001 | c0002 | t0014 | g0237 | SAS | GIH | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | GIH | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02109 | hp1 | a0001 | c0001 | t0045 | g0113 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0045 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03471 | hp2 | a0001 | c0001 | t0024 | g0234 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG06807 | hp1 | a0001 | c0015 | t0001 | g0144 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG06807 | hp2 | a0003 | c0006 | t0021 | g0229 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18955 | hp2 | a0001 | c0002 | t0014 | g0241 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA21309 | hp2 | a0001 | c0001 | t0026 | g0141 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0104 | REF | REF | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0012 | REF | REF | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114628140
|
A | G | 1 | a0004 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.364A>G | p.Ser122Gly | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/9 | 716/4490 | 364/1029 | 122/342 | chr9 | 114628140 | ||
chr9:114633781
|
C | T | 1 | a0005 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.488C>T | p.Thr163Met | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/9 | 840/4490 | 488/1029 | 163/342 | chr9 | 114633781 | ||
chr9:114633840
|
G | C | 1 | a0003 | 2 | HG03130.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.547G>C | p.Val183Leu | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/9 | 899/4490 | 547/1029 | 183/342 | chr9 | 114633840 | ||
chr9:114638549
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.672G>T | p.Leu224Phe | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1024/4490 | 672/1029 | 224/342 | chr9 | 114638549 | ||
chr9:114638581
|
T | C | 1 | a0007 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.704T>C | p.Val235Ala | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1056/4490 | 704/1029 | 235/342 | chr9 | 114638581 | ||
chr9:114638587
|
A | T | 1 | a0008 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.710A>T | p.Glu237Val | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1062/4490 | 710/1029 | 237/342 | chr9 | 114638587 | ||
chr9:114638667
|
A | G | 1 | a0002 | 3 | HG02647.hp2 HG03098.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.790A>G | p.Asn264Asp | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1142/4490 | 790/1029 | 264/342 | chr9 | 114638667 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114624426
|
C | T | 1 | a0001c0015 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.183C>T | p.Ala61Ala | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/9 | 535/4490 | 183/1029 | 61/342 | chr9 | 114624426 | ||
chr9:114624439
|
C | T | 1 | a0001c0002 | 23 | HG00423.hp2 HG02027.hp2 HG02155.hp2 others(20): Show |
synonymous_variant | LOW | c.196C>T | p.Leu66Leu | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/9 | 548/4490 | 196/1029 | 66/342 | chr9 | 114624439 | ||
chr9:114626901
|
C | A | 1 | a0001c0007 | 1 | NA19055.hp2 | splice_region_variant&synonymous_variant | LOW | c.219C>A | p.Val73Val | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/9 | 571/4490 | 219/1029 | 73/342 | chr9 | 114626901 | ||
chr9:114626985
|
T | C | 2 | a0001c0003a0007c0008 | 4 | HG00544.hp1 NA18964.hp2 NA19001.hp1 others(1): Show |
synonymous_variant | LOW | c.303T>C | p.Pro101Pro | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/9 | 655/4490 | 303/1029 | 101/342 | chr9 | 114626985 | ||
chr9:114638546
|
C | T | 1 | a0001c0012 | 1 | HG02148.hp1 | splice_region_variant&synonymous_variant | LOW | c.669C>T | p.Ser223Ser | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1021/4490 | 669/1029 | 223/342 | chr9 | 114638546 | ||
chr9:114638651
|
C | T | 1 | a0001c0005 | 3 | NA18965.hp1 NA18966.hp1 NA19079.hp1 |
synonymous_variant | LOW | c.774C>T | p.Pro258Pro | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1126/4490 | 774/1029 | 258/342 | chr9 | 114638651 | ||
chr9:114638723
|
G | A | 1 | a0001c0009 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.846G>A | p.Pro282Pro | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1198/4490 | 846/1029 | 282/342 | chr9 | 114638723 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114611304
|
C | T | 5 | a0001c0001t0007a0001c0001t0017a0001c0001t0049others(2): Show | 18 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-339C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5892 | chr9 | 114611304 | |||||
chr9:114611395
|
G | A | 1 | a0001c0001t0049 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-248G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5801 | chr9 | 114611395 | |||||
chr9:114611426
|
G | A | 1 | a0001c0001t0028 | 1 | HG01243.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-217G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | chr9 | 114611426 | ||||||
chr9:114611431
|
G | A | 1 | a0002c0004t0029 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5765 | chr9 | 114611431 | |||||
chr9:114611444
|
G | C | 8 | a0001c0001t0012a0001c0001t0019a0001c0001t0030others(5): Show | 32 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-199G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5752 | chr9 | 114611444 | |||||
chr9:114611486
|
G | C | 1 | a0001c0001t0020 | 2 | NA19010.hp2 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-157G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5710 | chr9 | 114611486 | |||||
chr9:114611533
|
T | C | 1 | a0001c0001t0034 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5663 | chr9 | 114611533 | |||||
chr9:114611533
|
T | TGGC | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0016others(17): Show | 176 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(173): Show |
5_prime_UTR_variant | MODIFIER | c.-87_-85dupGCG | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | ||||
chr9:114611533
|
T | TGGCGGC | 11 | a0001c0001t0008a0001c0001t0010a0001c0001t0012others(8): Show | 53 | HG00423.hp2 HG00438.hp1 HG01071.hp1 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-90_-85dupGCGGCG | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | ||||
chr9:114611533
|
T | TGGCGGCG others(2): Show |
3 | a0001c0001t0019a0001c0001t0032a0001c0002t0033 | 4 | HG00140.hp1 HG01978.hp1 NA18989.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-85dupGCGGCGGC others(1): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | ||||
chr9:114611533
|
TGGCGGCG others(2): Show |
T | 2 | a0001c0001t0011a0003c0006t0021 | 8 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-85delGCGGCGGC others(1): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5638 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | ||||
chr9:114611550
|
G | GCGGCGGC others(5): Show |
4 | a0001c0001t0004a0001c0001t0023a0001c0001t0040others(1): Show | 30 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-85_-84insGCGCCGGC others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611550 | ||||
chr9:114643365
|
T | G | 5 | a0001c0001t0007a0001c0001t0009a0001c0001t0035others(2): Show | 23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*52T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 52 | chr9 | 114643365 | |||||
chr9:114643888
|
C | T | 1 | a0001c0001t0026 | 2 | HG02257.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 575 | chr9 | 114643888 | |||||
chr9:114644018
|
T | C | 1 | a0001c0001t0036 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 705 | chr9 | 114644018 | |||||
chr9:114644101
|
A | G | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(9): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*788A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 788 | chr9 | 114644101 | |||||
chr9:114644236
|
C | G | 1 | a0001c0001t0046 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*923C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 923 | chr9 | 114644236 | |||||
chr9:114644321
|
A | G | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(9): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1008A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1008 | chr9 | 114644321 | |||||
chr9:114644557
|
A | G | 1 | a0001c0001t0045 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1244A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1244 | chr9 | 114644557 | |||||
chr9:114644594
|
G | GA | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(9): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1290dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1291 | INFO_REALIGN_3_PRIME | chr9 | 114644594 | ||||
chr9:114644683
|
C | T | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(9): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1370C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1370 | chr9 | 114644683 | |||||
chr9:114644685
|
G | A | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(9): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1372G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1372 | chr9 | 114644685 | |||||
chr9:114644797
|
A | AT | 4 | a0001c0001t0007a0001c0001t0041a0001c0001t0044others(1): Show | 14 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1497dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1498 | INFO_REALIGN_3_PRIME | chr9 | 114644797 | ||||
chr9:114644879
|
C | A | 1 | a0001c0001t0037 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1566C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1566 | chr9 | 114644879 | |||||
chr9:114644885
|
C | T | 2 | a0001c0001t0025a0001c0001t0045 | 3 | HG02109.hp1 HG02280.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1572C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1572 | chr9 | 114644885 | |||||
chr9:114644886
|
A | G | 37 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(34): Show | 170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1573A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1573 | chr9 | 114644886 | |||||
chr9:114644973
|
T | G | 12 | a0001c0001t0003a0001c0001t0018a0001c0001t0023others(9): Show | 46 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1660T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1660 | chr9 | 114644973 | |||||
chr9:114645044
|
C | T | 2 | a0001c0001t0015a0001c0001t0043 | 5 | HG00738.hp2 HG01074.hp1 HG01257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1731C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1731 | chr9 | 114645044 | |||||
chr9:114645061
|
G | C | 13 | a0001c0001t0003a0001c0001t0018a0001c0001t0023others(10): Show | 47 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1748G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1748 | chr9 | 114645061 | |||||
chr9:114645420
|
A | G | 1 | a0001c0001t0038 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2107 | chr9 | 114645420 | |||||
chr9:114645509
|
G | T | 1 | a0001c0001t0031 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2196G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2196 | chr9 | 114645509 | |||||
chr9:114645556
|
G | A | 6 | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(3): Show | 24 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2243G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2243 | chr9 | 114645556 | |||||
chr9:114645579
|
A | C | 2 | a0001c0001t0008a0001c0001t0012 | 15 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2266A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2266 | chr9 | 114645579 | |||||
chr9:114645643
|
C | T | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(9): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2330C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2330 | chr9 | 114645643 | |||||
chr9:114645644
|
G | T | 10 | a0001c0001t0003a0001c0001t0023a0001c0001t0031others(7): Show | 42 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2331G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2331 | chr9 | 114645644 | |||||
chr9:114645645
|
G | T | 10 | a0001c0001t0003a0001c0001t0023a0001c0001t0031others(7): Show | 42 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2332G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2332 | chr9 | 114645645 | |||||
chr9:114645781
|
T | C | 1 | a0001c0001t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2468T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2468 | chr9 | 114645781 | |||||
chr9:114645821
|
A | G | 5 | a0001c0001t0007a0001c0001t0009a0001c0001t0035others(2): Show | 23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2508A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2508 | chr9 | 114645821 | |||||
chr9:114645899
|
G | T | 1 | a0001c0001t0048 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2586G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2586 | chr9 | 114645899 | |||||
chr9:114645962
|
A | T | 1 | a0001c0001t0050 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2649A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2649 | chr9 | 114645962 | |||||
chr9:114645975
|
T | A | 12 | a0001c0001t0003a0001c0001t0018a0001c0001t0023others(9): Show | 46 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2662T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2662 | chr9 | 114645975 | |||||
chr9:114646180
|
G | A | 1 | a0001c0001t0041 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2867G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2867 | chr9 | 114646180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114611580
|
C | G | 1 | a0001c0001t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-79+16C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611580 | ||||||
chr9:114611626
|
G | T | 1 | a0001c0001t0048g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-79+62G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611626 | ||||||
chr9:114611742
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0016g0257 | 2 | HG02109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-79+178C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611742 | ||||||
chr9:114611800
|
G | A | 2 | a0001c0001t0016g0045a0001c0001t0016g0046 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-79+236G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611800 | ||||||
chr9:114611858
|
A | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0250a0001c0001t0002g0251others(5): Show | 11 | HG02074.hp2 HG02129.hp1 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.-79+294A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611858 | ||||||
chr9:114612032
|
C | G | 1 | a0001c0001t0001g0249 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-79+468C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612032 | ||||||
chr9:114612127
|
T | C | 9 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(6): Show | 13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-79+563T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612127 | ||||||
chr9:114612236
|
C | T | 1 | a0001c0001t0009g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-79+672C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612236 | ||||||
chr9:114612434
|
C | T | 18 | a0001c0001t0012g0042a0001c0001t0012g0043a0001c0001t0012g0239others(15): Show | 32 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(29): Show |
intron_variant | MODIFIER | c.-79+870C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612434 | ||||||
chr9:114612453
|
CCTT | C | 23 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(20): Show | 30 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-79+892_-79+894del others(3): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114612453 | |||||
chr9:114612634
|
C | G | 5 | a0001c0001t0009g0233a0001c0001t0024g0234a0002c0004t0013g0230others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-79+1070C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612634 | ||||||
chr9:114612690
|
C | T | 1 | a0003c0006t0021g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-79+1126C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612690 | ||||||
chr9:114612745
|
C | G | 1 | a0001c0001t0006g0228 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-79+1181C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612745 | ||||||
chr9:114613156
|
C | T | 1 | a0001c0001t0024g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-79+1592C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613156 | ||||||
chr9:114613215
|
A | G | 1 | a0001c0001t0024g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-79+1651A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613215 | ||||||
chr9:114613274
|
G | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(206): Show | 311 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-79+1710G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613274 | ||||||
chr9:114613450
|
A | T | 1 | a0001c0001t0018g0227 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-79+1886A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613450 | ||||||
chr9:114613496
|
A | G | 1 | a0001c0001t0027g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-79+1932A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613496 | ||||||
chr9:114613629
|
C | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(121): Show | 196 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.-79+2065C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613629 | ||||||
chr9:114613745
|
TTTTTGTT others(3): Show |
T | 1 | a0001c0001t0001g0110 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-79+2198_-79+2207d others(12): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114613745 | |||||
chr9:114613750
|
G | T | 1 | a0001c0001t0034g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-79+2186G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613750 | ||||||
chr9:114613933
|
C | T | 21 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(18): Show | 28 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-79+2369C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613933 | ||||||
chr9:114613939
|
T | G | 21 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(18): Show | 28 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-79+2375T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613939 | ||||||
chr9:114614006
|
C | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(261): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.-79+2442C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614006 | ||||||
chr9:114614116
|
G | A | 1 | a0001c0001t0002g0023 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-79+2552G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614116 | ||||||
chr9:114614181
|
T | G | 14 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(11): Show | 17 | HG01074.hp1 HG01192.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-79+2617T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614181 | ||||||
chr9:114614497
|
C | T | 15 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(12): Show | 17 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78-2621C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614497 | ||||||
chr9:114614746
|
A | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(263): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-78-2372A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614746 | ||||||
chr9:114614892
|
C | CT | 54 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(51): Show | 71 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.-78-2204dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | |||||
chr9:114614892
|
C | CTT | 8 | a0001c0001t0003g0014a0001c0001t0003g0198a0001c0001t0003g0199others(5): Show | 11 | HG00544.hp2 HG00609.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78-2205_-78-2204d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | |||||
chr9:114614892
|
CT | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0016g0045others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78-2204delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | |||||
chr9:114614892
|
CTTTT | C | 6 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(3): Show | 10 | HG00438.hp1 HG01884.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-78-2207_-78-2204d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | |||||
chr9:114614892
|
CTTTTTTT others(4): Show |
C | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(41): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-78-2214_-78-2204d others(13): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | |||||
chr9:114614935
|
C | T | 1 | a0001c0001t0027g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-78-2183C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614935 | ||||||
chr9:114614936
|
G | A | 20 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(17): Show | 27 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-78-2182G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614936 | ||||||
chr9:114615058
|
G | A | 1 | a0001c0001t0008g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-78-2060G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615058 | ||||||
chr9:114615095
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18994.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-78-2023C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615095 | ||||||
chr9:114615297
|
T | C | 1 | a0001c0001t0016g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-78-1821T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615297 | ||||||
chr9:114615485
|
G | T | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1633G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615485 | ||||||
chr9:114615493
|
A | G | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1625A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615493 | ||||||
chr9:114615495
|
A | G | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1623A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615495 | ||||||
chr9:114615497
|
T | A | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1621T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615497 | ||||||
chr9:114615525
|
C | G | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1593C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615525 | ||||||
chr9:114615528
|
T | A | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1590T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615528 | ||||||
chr9:114615539
|
T | C | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1579T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615539 | ||||||
chr9:114615545
|
T | C | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1573T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615545 | ||||||
chr9:114615546
|
A | T | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1572A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615546 | ||||||
chr9:114615547
|
A | G | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1571A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615547 | ||||||
chr9:114615550
|
C | T | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1568C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615550 | ||||||
chr9:114615553
|
T | A | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1565T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615553 | ||||||
chr9:114615563
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(206): Show | 311 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-78-1555G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615563 | ||||||
chr9:114615567
|
C | CCTAGAAC others(20): Show |
2 | a0001c0001t0013g0211a0001c0001t0013g0213 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-78-1548_-78-1522d others(29): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114615567 | |||||
chr9:114615592
|
A | C | 1 | a0001c0001t0004g0073 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-78-1526A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615592 | ||||||
chr9:114615729
|
T | A | 1 | a0001c0001t0034g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-78-1389T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615729 | ||||||
chr9:114615810
|
C | T | 1 | a0006c0011t0002g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-78-1308C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615810 | ||||||
chr9:114615818
|
C | A | 2 | a0001c0001t0007g0225a0001c0001t0007g0226 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-78-1300C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615818 | ||||||
chr9:114615827
|
T | A | 1 | a0001c0001t0034g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-78-1291T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615827 | ||||||
chr9:114615862
|
T | C | 22 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(19): Show | 29 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-78-1256T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615862 | ||||||
chr9:114615870
|
T | G | 2 | a0001c0001t0025g0114a0001c0001t0045g0113 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-78-1248T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615870 | ||||||
chr9:114615872
|
A | G | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-78-1246A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615872 | ||||||
chr9:114616000
|
TTTTTCTT others(5): Show |
T | 16 | a0001c0001t0012g0042a0001c0001t0012g0043a0001c0001t0012g0239others(13): Show | 29 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.-78-1106_-78-1095d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616000 | |||||
chr9:114616005
|
CTTTTTTC others(6): Show |
C | 1 | a0001c0002t0005g0247 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1106_-78-1094d others(15): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616005 | |||||
chr9:114616017
|
C | CT | 19 | a0001c0001t0001g0175a0001c0001t0001g0197a0001c0001t0004g0070others(16): Show | 22 | HG00738.hp2 HG01192.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-78-1085dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616017 | |||||
chr9:114616017
|
CT | C | 30 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0177others(27): Show | 42 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-78-1085delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616017 | |||||
chr9:114616200
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-78-918A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616200 | ||||||
chr9:114616205
|
C | T | 1 | a0001c0001t0002g0017 | 3 | NA18972.hp1 NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-78-913C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616205 | ||||||
chr9:114616256
|
G | C | 65 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(62): Show | 81 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.-78-862G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616256 | ||||||
chr9:114616267
|
G | A | 1 | a0001c0002t0024g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-78-851G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616267 | ||||||
chr9:114616293
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0042g0122others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-825G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616293 | ||||||
chr9:114616304
|
C | T | 1 | a0001c0001t0004g0069 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-78-814C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616304 | ||||||
chr9:114616357
|
GTTTGTT | G | 7 | a0001c0001t0006g0020a0001c0001t0006g0203a0001c0001t0006g0204others(4): Show | 9 | HG01192.hp2 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-78-740_-78-735del others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616357 | |||||
chr9:114616357
|
GTTTGTTT others(5): Show |
G | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-78-746_-78-735del others(12): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616357 | |||||
chr9:114616367
|
GTTT | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(41): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-78-748_-78-746del others(3): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616367 | |||||
chr9:114616461
|
G | T | 1 | a0001c0001t0034g0200 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-78-657G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616461 | ||||||
chr9:114616526
|
C | A | 1 | a0001c0001t0051g0215 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-78-592C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616526 | ||||||
chr9:114616526
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-78-592C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616526 | ||||||
chr9:114616528
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-78-590G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616528 | ||||||
chr9:114616610
|
C | T | 1 | a0001c0001t0024g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-78-508C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616610 | ||||||
chr9:114616646
|
G | A | 1 | a0001c0001t0008g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-78-472G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616646 | ||||||
chr9:114616739
|
A | G | 1 | a0001c0001t0049g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-78-379A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616739 | ||||||
chr9:114616765
|
T | G | 1 | a0001c0001t0002g0075 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-78-353T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616765 | ||||||
chr9:114617006
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(206): Show | 311 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-78-112G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617006 | ||||||
chr9:114617009
|
C | T | 2 | a0003c0006t0021g0172a0003c0006t0021g0229 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-78-109C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617009 | ||||||
chr9:114617010
|
G | C | 9 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(6): Show | 13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78-108G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617010 | ||||||
chr9:114617107
|
G | A | 1 | a0001c0001t0049g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-78-11G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617107 | ||||||
chr9:114617309
|
C | G | 15 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(12): Show | 18 | HG00738.hp2 HG01074.hp1 HG01192.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.106+8C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617309 | ||||||
chr9:114617469
|
C | G | 2 | a0001c0001t0025g0114a0001c0001t0045g0113 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.106+168C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617469 | ||||||
chr9:114617677
|
C | T | 2 | a0003c0006t0021g0172a0003c0006t0021g0229 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.106+376C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617677 | ||||||
chr9:114617813
|
C | A | 20 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(17): Show | 27 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.106+512C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617813 | ||||||
chr9:114617878
|
TA | T | 7 | a0001c0001t0001g0131a0001c0001t0003g0188a0001c0001t0007g0225others(4): Show | 7 | HG01167.hp1 HG01515.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+578delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617878 | ||||||
chr9:114617879
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(168): Show | 265 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.106+578A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617879 | ||||||
chr9:114617879
|
AT | A | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.106+586delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114617879 | |||||
chr9:114617881
|
T | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | NA18948.hp2 NA18962.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.106+580T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617881 | ||||||
chr9:114617887
|
T | A | 4 | a0001c0001t0009g0233a0002c0004t0013g0230a0002c0004t0013g0232others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+586T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617887 | ||||||
chr9:114617947
|
G | A | 15 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(12): Show | 18 | HG00738.hp2 HG01074.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+646G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617947 | ||||||
chr9:114618119
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.106+818C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618119 | ||||||
chr9:114618132
|
C | G | 1 | a0001c0001t0003g0186 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.106+831C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618132 | ||||||
chr9:114618161
|
G | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG00673.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.106+860G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618161 | ||||||
chr9:114618202
|
T | G | 17 | a0001c0001t0012g0042a0001c0001t0012g0043a0001c0001t0012g0239others(14): Show | 30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+901T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618202 | ||||||
chr9:114618523
|
T | A | 1 | a0001c0001t0011g0133 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.106+1222T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618523 | ||||||
chr9:114618567
|
G | A | 1 | a0001c0001t0009g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.106+1266G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618567 | ||||||
chr9:114618604
|
G | A | 17 | a0001c0001t0012g0042a0001c0001t0012g0043a0001c0001t0012g0239others(14): Show | 30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+1303G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618604 | ||||||
chr9:114618662
|
CA | C | 18 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(15): Show | 25 | HG00609.hp1 HG00673.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.106+1372delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114618662 | |||||
chr9:114618673
|
A | G | 1 | a0001c0001t0002g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.106+1372A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618673 | ||||||
chr9:114618742
|
G | T | 4 | a0001c0001t0009g0233a0002c0004t0013g0230a0002c0004t0013g0232others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1441G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618742 | ||||||
chr9:114618743
|
GT | G | 4 | a0001c0001t0009g0233a0002c0004t0013g0230a0002c0004t0013g0232others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1443delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618743 | ||||||
chr9:114618784
|
T | C | 1 | a0001c0001t0009g0098 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.106+1483T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618784 | ||||||
chr9:114618858
|
G | A | 9 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(6): Show | 13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.106+1557G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618858 | ||||||
chr9:114618882
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(251): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.106+1581T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618882 | ||||||
chr9:114618946
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.106+1645A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618946 | ||||||
chr9:114619073
|
A | T | 2 | a0003c0006t0021g0172a0003c0006t0021g0229 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.106+1772A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619073 | ||||||
chr9:114619276
|
C | T | 1 | a0001c0001t0007g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.106+1975C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619276 | ||||||
chr9:114619282
|
C | T | 3 | a0001c0001t0006g0204a0001c0001t0006g0205a0001c0001t0006g0210 | 3 | HG01884.hp2 HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.106+1981C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619282 | ||||||
chr9:114619288
|
C | T | 15 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(12): Show | 18 | HG00738.hp2 HG01074.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+1987C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619288 | ||||||
chr9:114619291
|
G | T | 5 | a0001c0001t0015g0202a0001c0001t0015g0207a0001c0001t0015g0208others(2): Show | 5 | HG00738.hp2 HG01074.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+1990G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619291 | ||||||
chr9:114619293
|
G | GCA | 49 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(46): Show | 80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.106+2019_106+2020d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | |||||
chr9:114619293
|
G | GCACA | 3 | a0001c0001t0002g0074a0001c0001t0002g0076a0001c0001t0028g0179 | 3 | HG01243.hp2 HG02027.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.106+2017_106+2020d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | |||||
chr9:114619293
|
GCA | G | 31 | a0001c0001t0002g0023a0001c0001t0002g0093a0001c0001t0002g0104others(28): Show | 39 | HG00609.hp1 HG00673.hp1 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.106+2019_106+2020d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | |||||
chr9:114619293
|
GCACA | G | 3 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0185 | 3 | HG00423.hp1 NA18948.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.106+2017_106+2020d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | |||||
chr9:114619293
|
GCACACAC others(1): Show |
G | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.106+2013_106+2020d others(10): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | |||||
chr9:114619293
|
GCACACAC others(5): Show |
G | 3 | a0001c0001t0001g0120a0001c0001t0001g0175a0001c0001t0001g0197 | 3 | NA18941.hp1 NA18955.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.106+2009_106+2020d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | |||||
chr9:114619483
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(250): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.106+2182G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619483 | ||||||
chr9:114619578
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0044g0035 | 2 | HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.106+2277C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619578 | ||||||
chr9:114619604
|
C | T | 17 | a0001c0001t0012g0042a0001c0001t0012g0043a0001c0001t0012g0239others(14): Show | 30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+2303C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619604 | ||||||
chr9:114619770
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.106+2469G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619770 | ||||||
chr9:114619864
|
C | T | 28 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(25): Show | 40 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.106+2563C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619864 | ||||||
chr9:114619868
|
CT | C | 9 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(6): Show | 13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.106+2576delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619868 | |||||
chr9:114619972
|
G | A | 3 | a0001c0001t0017g0040a0001c0001t0017g0223a0001c0001t0017g0224 | 4 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2671G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619972 | ||||||
chr9:114620071
|
C | T | 4 | a0001c0001t0017g0040a0001c0001t0017g0223a0001c0001t0017g0224others(1): Show | 5 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+2770C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620071 | ||||||
chr9:114620084
|
G | A | 59 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(56): Show | 93 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.106+2783G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620084 | ||||||
chr9:114620108
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(91): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.106+2807G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620108 | ||||||
chr9:114620120
|
CAGGAGAA others(21): Show |
C | 1 | a0001c0001t0004g0073 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.106+2823_106+2850d others(30): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114620120 | |||||
chr9:114620170
|
G | A | 37 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(34): Show | 49 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.106+2869G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620170 | ||||||
chr9:114620243
|
GTTAC | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(92): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.106+2950_106+2953d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114620243 | |||||
chr9:114620253
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.106+2952T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620253 | ||||||
chr9:114620283
|
T | G | 3 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089 | 3 | HG02818.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.106+2982T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620283 | ||||||
chr9:114620305
|
C | T | 2 | a0001c0001t0007g0225a0001c0001t0007g0226 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.106+3004C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620305 | ||||||
chr9:114620306
|
G | A | 1 | a0001c0001t0004g0058 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.106+3005G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620306 | ||||||
chr9:114620322
|
G | A | 1 | a0001c0001t0006g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106+3021G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620322 | ||||||
chr9:114620370
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.106+3069G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620370 | ||||||
chr9:114620402
|
G | A | 1 | a0001c0001t0004g0073 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.106+3101G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620402 | ||||||
chr9:114620448
|
C | T | 1 | a0001c0001t0010g0168 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.106+3147C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620448 | ||||||
chr9:114620457
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0166a0001c0001t0001g0194others(1): Show | 4 | HG00733.hp2 HG02004.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+3156C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620457 | ||||||
chr9:114620493
|
C | T | 1 | a0001c0001t0009g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+3192C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620493 | ||||||
chr9:114620774
|
C | T | 1 | a0001c0001t0049g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.106+3473C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620774 | ||||||
chr9:114620775
|
G | A | 2 | a0001c0001t0007g0225a0001c0001t0007g0226 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.106+3474G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620775 | ||||||
chr9:114620926
|
C | CA | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(89): Show | 153 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.107-3415dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114620926 | |||||
chr9:114621035
|
A | C | 17 | a0001c0001t0012g0042a0001c0001t0012g0043a0001c0001t0012g0239others(14): Show | 30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.107-3315A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621035 | ||||||
chr9:114621124
|
G | C | 1 | a0001c0001t0003g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.107-3226G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621124 | ||||||
chr9:114621245
|
T | C | 35 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(32): Show | 48 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.107-3105T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621245 | ||||||
chr9:114621248
|
C | T | 11 | a0001c0001t0003g0184a0001c0001t0009g0233a0001c0001t0009g0248others(8): Show | 12 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.107-3102C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621248 | ||||||
chr9:114621310
|
C | T | 1 | a0001c0001t0010g0163 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.107-3040C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621310 | ||||||
chr9:114621345
|
C | CA | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(143): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.107-2991dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114621345 | |||||
chr9:114621345
|
C | CAA | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-2992_107-2991d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114621345 | |||||
chr9:114621366
|
G | T | 44 | a0001c0001t0001g0127a0001c0001t0001g0164a0001c0001t0002g0002others(41): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.107-2984G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621366 | ||||||
chr9:114621383
|
A | G | 1 | a0001c0001t0013g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-2967A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621383 | ||||||
chr9:114621542
|
T | C | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.107-2808T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621542 | ||||||
chr9:114621639
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(132): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.107-2711G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621639 | ||||||
chr9:114621675
|
A | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.107-2675A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621675 | ||||||
chr9:114621681
|
A | G | 3 | a0001c0001t0013g0213a0001c0001t0025g0114a0001c0001t0045g0113 | 3 | HG02109.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.107-2669A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621681 | ||||||
chr9:114621795
|
C | T | 7 | a0001c0001t0009g0233a0001c0001t0009g0248a0001c0001t0013g0103others(4): Show | 7 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-2555C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621795 | ||||||
chr9:114621943
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(253): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.107-2407G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621943 | ||||||
chr9:114621959
|
C | T | 14 | a0001c0001t0006g0228a0001c0001t0008g0009a0001c0001t0008g0047others(11): Show | 20 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.107-2391C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621959 | ||||||
chr9:114622404
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-1946C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622404 | ||||||
chr9:114622492
|
T | C | 2 | a0001c0001t0016g0045a0001c0001t0016g0046 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107-1858T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622492 | ||||||
chr9:114622718
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(204): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.107-1632G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622718 | ||||||
chr9:114622802
|
G | A | 1 | a0001c0001t0022g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107-1548G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622802 | ||||||
chr9:114622846
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.107-1504T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622846 | ||||||
chr9:114622850
|
G | A | 1 | a0001c0001t0004g0059 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.107-1500G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622850 | ||||||
chr9:114622941
|
T | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(231): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.107-1409T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622941 | ||||||
chr9:114623076
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.107-1274A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623076 | ||||||
chr9:114623094
|
A | AAAC | 4 | a0001c0001t0002g0091a0001c0001t0026g0140a0001c0001t0026g0141others(1): Show | 4 | HG01074.hp2 HG02257.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1229_107-1227d others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114623094 | |||||
chr9:114623094
|
A | C | 12 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(9): Show | 13 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-1256A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623094 | ||||||
chr9:114623094
|
AAAC | A | 39 | a0001c0001t0002g0260a0001c0001t0003g0004a0001c0001t0003g0014others(36): Show | 51 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.107-1229_107-1227d others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114623094 | |||||
chr9:114623097
|
C | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0166a0001c0001t0001g0194others(1): Show | 4 | HG00733.hp2 HG02004.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-1253C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623097 | ||||||
chr9:114623111
|
A | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(28): Show | 43 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.107-1239A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623111 | ||||||
chr9:114623211
|
C | T | 2 | a0003c0006t0021g0172a0003c0006t0021g0229 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.107-1139C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623211 | ||||||
chr9:114623295
|
G | A | 1 | a0001c0001t0002g0024 | 2 | NA18962.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.107-1055G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623295 | ||||||
chr9:114623383
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(229): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.107-967C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623383 | ||||||
chr9:114623637
|
C | T | 1 | a0001c0001t0017g0040 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.107-713C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623637 | ||||||
chr9:114623712
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.107-638G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623712 | ||||||
chr9:114623812
|
C | G | 3 | a0002c0004t0013g0230a0002c0004t0013g0232a0002c0004t0029g0231 | 3 | HG02647.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.107-538C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623812 | ||||||
chr9:114624068
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(144): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.107-282A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624068 | ||||||
chr9:114624114
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(252): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.107-236T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624114 | ||||||
chr9:114624136
|
G | C | 1 | a0001c0001t0004g0021 | 2 | NA18961.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.107-214G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624136 | ||||||
chr9:114624285
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.107-65G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624285 | ||||||
chr9:114624547
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.216+88T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624547 | ||||||
chr9:114624679
|
A | T | 32 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(29): Show | 44 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.216+220A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624679 | ||||||
chr9:114624724
|
A | G | 1 | a0001c0001t0049g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.216+265A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624724 | ||||||
chr9:114624754
|
C | T | 1 | a0001c0001t0028g0179 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.216+295C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624754 | ||||||
chr9:114624755
|
G | A | 2 | a0001c0001t0013g0211a0001c0001t0013g0213 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.216+296G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624755 | ||||||
chr9:114624885
|
A | G | 4 | a0001c0001t0025g0114a0001c0001t0045g0113a0003c0006t0021g0172others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+426A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624885 | ||||||
chr9:114624977
|
A | G | 14 | a0001c0001t0006g0228a0001c0001t0007g0039a0001c0001t0007g0216others(11): Show | 15 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+518A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624977 | ||||||
chr9:114625393
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(228): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.216+934T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625393 | ||||||
chr9:114625427
|
G | T | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.216+968G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625427 | ||||||
chr9:114625443
|
CT | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(169): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.216+1002delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 114625443 | |||||
chr9:114625443
|
CTT | C | 48 | a0001c0001t0001g0111a0001c0001t0001g0143a0001c0001t0001g0166others(45): Show | 62 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.216+1001_216+1002d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 114625443 | |||||
chr9:114625655
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.216+1196C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625655 | ||||||
chr9:114625657
|
G | C | 5 | a0001c0001t0015g0202a0001c0001t0015g0207a0001c0001t0015g0208others(2): Show | 5 | HG00738.hp2 HG01074.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+1198G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625657 | ||||||
chr9:114625993
|
A | G | 3 | a0001c0001t0011g0013a0001c0001t0011g0133a0001c0001t0011g0155 | 6 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-906A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625993 | ||||||
chr9:114626071
|
C | T | 1 | a0001c0001t0010g0168 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.217-828C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626071 | ||||||
chr9:114626201
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.217-698A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626201 | ||||||
chr9:114626238
|
C | G | 3 | a0002c0004t0013g0230a0002c0004t0013g0232a0002c0004t0029g0231 | 3 | HG02647.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-661C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626238 | ||||||
chr9:114626280
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.217-619G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626280 | ||||||
chr9:114626333
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.217-566C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626333 | ||||||
chr9:114626650
|
C | T | 8 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(5): Show | 11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.217-249C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626650 | ||||||
chr9:114626764
|
C | G | 1 | a0001c0001t0009g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217-135C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626764 | ||||||
chr9:114626770
|
C | T | 3 | a0001c0001t0025g0114a0001c0001t0025g0159a0001c0001t0045g0113 | 3 | HG02109.hp1 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.217-129C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626770 | ||||||
chr9:114627198
|
C | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(231): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.324+192C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627198 | ||||||
chr9:114627311
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(135): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.324+305T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627311 | ||||||
chr9:114627428
|
A | G | 5 | a0001c0002t0005g0003a0001c0002t0005g0235a0001c0002t0005g0236others(2): Show | 15 | HG00423.hp2 NA18612.hp2 NA18982.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+422A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627428 | ||||||
chr9:114627701
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.325-400G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627701 | ||||||
chr9:114627838
|
C | T | 6 | a0001c0002t0014g0237a0001c0002t0014g0240a0001c0002t0014g0241others(3): Show | 6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-263C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627838 | ||||||
chr9:114627904
|
G | C | 1 | a0001c0001t0036g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.325-197G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627904 | ||||||
chr9:114627918
|
A | T | 18 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(15): Show | 24 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.325-183A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627918 | ||||||
chr9:114627923
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.325-178C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627923 | ||||||
chr9:114627936
|
C | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0249 | 2 | HG01099.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.325-165C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627936 | ||||||
chr9:114627944
|
C | T | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.325-157C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627944 | ||||||
chr9:114628020
|
C | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(133): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.325-81C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114628020 | ||||||
chr9:114628055
|
C | T | 18 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(15): Show | 24 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.325-46C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114628055 | ||||||
chr9:114628081
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.325-20C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114628081 | ||||||
chr9:114628256
|
A | C | 1 | a0002c0004t0013g0232 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.474+6A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628256 | ||||||
chr9:114628274
|
C | A | 1 | a0001c0001t0049g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.474+24C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628274 | ||||||
chr9:114628280
|
C | CT | 23 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(20): Show | 26 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+31dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114628280 | |||||
chr9:114628293
|
C | G | 13 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(10): Show | 19 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.474+43C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628293 | ||||||
chr9:114628293
|
C | T | 1 | a0001c0001t0007g0219 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.474+43C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628293 | ||||||
chr9:114628397
|
C | A | 27 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(24): Show | 35 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.474+147C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628397 | ||||||
chr9:114628459
|
G | A | 3 | a0001c0001t0017g0040a0001c0001t0017g0223a0001c0001t0017g0224 | 4 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+209G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628459 | ||||||
chr9:114628518
|
G | A | 2 | a0001c0001t0016g0045a0001c0001t0016g0046 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.474+268G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628518 | ||||||
chr9:114628861
|
C | T | 28 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(25): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+611C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628861 | ||||||
chr9:114629045
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(208): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.474+795A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629045 | ||||||
chr9:114629077
|
A | T | 2 | a0001c0001t0025g0114a0001c0001t0045g0113 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.474+827A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629077 | ||||||
chr9:114629309
|
C | T | 28 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(25): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1059C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629309 | ||||||
chr9:114629417
|
T | C | 1 | a0001c0001t0048g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474+1167T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629417 | ||||||
chr9:114629456
|
C | T | 2 | a0001c0001t0018g0227a0001c0001t0028g0179 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.474+1206C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629456 | ||||||
chr9:114629755
|
C | T | 2 | a0001c0001t0018g0227a0001c0001t0028g0179 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.474+1505C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629755 | ||||||
chr9:114629762
|
T | C | 2 | a0001c0001t0016g0045a0001c0001t0016g0046 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.474+1512T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629762 | ||||||
chr9:114629808
|
G | A | 28 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(25): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1558G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629808 | ||||||
chr9:114629826
|
C | T | 6 | a0001c0002t0014g0237a0001c0002t0014g0240a0001c0002t0014g0241others(3): Show | 6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+1576C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629826 | ||||||
chr9:114629942
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.474+1692C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629942 | ||||||
chr9:114630057
|
C | T | 33 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(30): Show | 45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.474+1807C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630057 | ||||||
chr9:114630089
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.474+1839T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630089 | ||||||
chr9:114630161
|
T | A | 1 | a0001c0001t0009g0098 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.474+1911T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630161 | ||||||
chr9:114630200
|
C | T | 8 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(5): Show | 11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+1950C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630200 | ||||||
chr9:114630230
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(207): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.474+1980C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630230 | ||||||
chr9:114630275
|
T | TATCCATC others(1): Show |
112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(109): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(10): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | |||||
chr9:114630275
|
T | TATCCATC others(5): Show |
24 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0134others(21): Show | 27 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | |||||
chr9:114630275
|
T | TATCCATC others(9): Show |
10 | a0001c0001t0001g0197a0001c0001t0015g0202a0001c0001t0015g0207others(7): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(18): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | |||||
chr9:114630275
|
T | TATCCATC others(13): Show |
4 | a0001c0001t0001g0152a0001c0001t0043g0195a0001c0001t0049g0212others(1): Show | 4 | HG00642.hp2 HG00738.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(22): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | |||||
chr9:114630275
|
T | TATCCATC others(17): Show |
2 | a0001c0002t0024g0121a0001c0002t0033g0243 | 2 | HG03017.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.474+2028_474+2029i others(26): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | |||||
chr9:114630279
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.474+2029T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630279 | ||||||
chr9:114630279
|
T | TATCCATC others(1): Show |
6 | a0001c0001t0006g0038a0001c0001t0006g0204a0001c0001t0006g0205others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+2059_474+2066d others(10): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | |||||
chr9:114630279
|
T | TATCCATC others(5): Show |
2 | a0001c0001t0006g0020a0001c0001t0006g0203 | 4 | HG01192.hp2 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+2055_474+2066d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | |||||
chr9:114630279
|
TATCC | T | 72 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(69): Show | 108 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.474+2063_474+2066d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | |||||
chr9:114630279
|
TATCCATC others(9): Show |
T | 1 | a0001c0001t0032g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.474+2051_474+2066d others(18): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | |||||
chr9:114630357
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(134): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.474+2107T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630357 | ||||||
chr9:114630359
|
C | T | 1 | a0001c0001t0017g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.474+2109C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630359 | ||||||
chr9:114630486
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.474+2236A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630486 | ||||||
chr9:114630531
|
A | G | 1 | a0001c0001t0006g0228 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.474+2281A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630531 | ||||||
chr9:114630548
|
C | T | 33 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(30): Show | 45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.474+2298C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630548 | ||||||
chr9:114630605
|
A | C | 8 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(5): Show | 11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+2355A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630605 | ||||||
chr9:114630609
|
T | G | 7 | a0001c0001t0001g0027a0001c0001t0002g0015a0001c0001t0002g0250others(4): Show | 11 | HG02015.hp1 HG02074.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+2359T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630609 | ||||||
chr9:114630805
|
C | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.474+2555C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630805 | ||||||
chr9:114630933
|
C | CTG | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.474+2685_474+2686d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630933 | |||||
chr9:114631167
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(134): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.475-2601G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631167 | ||||||
chr9:114631170
|
G | A | 12 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(9): Show | 18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.475-2598G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631170 | ||||||
chr9:114631172
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.475-2596G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631172 | ||||||
chr9:114631177
|
G | C | 1 | a0001c0015t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.475-2591G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631177 | ||||||
chr9:114631187
|
C | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0190 | 2 | HG01167.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.475-2581C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631187 | ||||||
chr9:114631246
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.475-2522T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631246 | ||||||
chr9:114631252
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-2516C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631252 | ||||||
chr9:114631282
|
C | CA | 27 | a0001c0001t0003g0118a0001c0001t0003g0185a0001c0001t0004g0006others(24): Show | 44 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.475-2462dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | |||||
chr9:114631282
|
C | CAA | 38 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(35): Show | 53 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.475-2463_475-2462d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | |||||
chr9:114631282
|
C | CAAA | 15 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0188others(12): Show | 20 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.475-2464_475-2462d others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | |||||
chr9:114631282
|
CAAAAAAA others(4): Show |
C | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(126): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.475-2472_475-2462d others(13): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | |||||
chr9:114631282
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0112a0001c0001t0001g0150 | 2 | NA18990.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.475-2473_475-2462d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | |||||
chr9:114631290
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0015g0207a0001c0001t0015g0209a0001c0001t0043g0195 | 3 | HG00738.hp2 HG01257.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.475-2465_475-2464i others(16): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631290 | |||||
chr9:114631290
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0015g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.475-2466_475-2465i others(15): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631290 | |||||
chr9:114631291
|
A | AAAAAAAA others(9): Show |
5 | a0001c0001t0013g0103a0001c0001t0024g0234a0002c0004t0013g0230others(2): Show | 5 | HG02647.hp2 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-2475_475-2460d others(18): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | |||||
chr9:114631291
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0013g0211a0001c0001t0013g0213 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.475-2463_475-2462i others(17): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | |||||
chr9:114631291
|
A | AAAAAAAA others(6): Show |
9 | a0001c0001t0015g0202a0001c0001t0016g0045a0001c0001t0016g0046others(6): Show | 9 | HG01074.hp1 HG02027.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-2465_475-2464i others(15): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | |||||
chr9:114631291
|
A | AAAAAAAA others(5): Show |
1 | a0001c0002t0014g0241 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.475-2466_475-2465i others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | |||||
chr9:114631292
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0002g0091a0001c0001t0048g0259 | 2 | HG01074.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.475-2465_475-2464i others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631292 | |||||
chr9:114631364
|
G | A | 5 | a0001c0001t0004g0021a0001c0001t0004g0060a0001c0001t0004g0062others(2): Show | 6 | NA18953.hp2 NA18961.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-2404G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631364 | ||||||
chr9:114631378
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-2390C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631378 | ||||||
chr9:114631388
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-2380C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631388 | ||||||
chr9:114631454
|
A | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-2314A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631454 | ||||||
chr9:114631456
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-2312C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631456 | ||||||
chr9:114631605
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0111others(6): Show | 16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.475-2163G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631605 | ||||||
chr9:114631625
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-2143G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631625 | ||||||
chr9:114631628
|
C | T | 1 | a0001c0001t0025g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-2140C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631628 | ||||||
chr9:114631654
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-2114C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631654 | ||||||
chr9:114631658
|
T | A | 2 | a0001c0001t0016g0045a0001c0001t0016g0046 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.475-2110T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631658 | ||||||
chr9:114631748
|
C | T | 33 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(30): Show | 45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.475-2020C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631748 | ||||||
chr9:114631779
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-1989T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631779 | ||||||
chr9:114631812
|
G | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-1956G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631812 | ||||||
chr9:114631826
|
C | T | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.475-1942C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631826 | ||||||
chr9:114631830
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(252): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.475-1938A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631830 | ||||||
chr9:114632006
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.475-1762T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632006 | ||||||
chr9:114632085
|
G | A | 28 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(25): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-1683G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632085 | ||||||
chr9:114632098
|
C | CA | 79 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0151others(76): Show | 112 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.475-1651dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632098 | |||||
chr9:114632098
|
C | CAA | 7 | a0001c0001t0003g0165a0001c0001t0003g0190a0001c0001t0004g0058others(4): Show | 7 | HG02738.hp2 HG03098.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-1652_475-1651d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632098 | |||||
chr9:114632098
|
CA | C | 7 | a0001c0001t0009g0233a0001c0001t0012g0239a0001c0001t0016g0045others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.475-1651delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632098 | |||||
chr9:114632135
|
G | A | 29 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(26): Show | 41 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.475-1633G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632135 | ||||||
chr9:114632142
|
G | A | 4 | a0001c0001t0016g0045a0001c0001t0016g0046a0001c0001t0048g0259others(1): Show | 4 | HG02257.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1626G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632142 | ||||||
chr9:114632177
|
AT | A | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1582delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632177 | |||||
chr9:114632315
|
A | G | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1453A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632315 | ||||||
chr9:114632474
|
T | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1294T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632474 | ||||||
chr9:114632543
|
C | T | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1225C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632543 | ||||||
chr9:114632557
|
C | T | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1211C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632557 | ||||||
chr9:114632605
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.475-1163G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632605 | ||||||
chr9:114632923
|
G | A | 55 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(52): Show | 77 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.475-845G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632923 | ||||||
chr9:114632942
|
C | A | 2 | a0001c0001t0048g0259a0001c0001t0049g0212 | 2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.475-826C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632942 | ||||||
chr9:114632947
|
T | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-821T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632947 | ||||||
chr9:114633143
|
A | T | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-625A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633143 | ||||||
chr9:114633159
|
T | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-609T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633159 | ||||||
chr9:114633162
|
AT | A | 102 | a0001c0001t0001g0128a0001c0001t0002g0078a0001c0001t0003g0004others(99): Show | 143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.475-589delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114633162 | |||||
chr9:114633171
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 11 | HG00639.hp1 HG01081.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-597T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633171 | ||||||
chr9:114633185
|
A | G | 107 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(104): Show | 148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.475-583A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633185 | ||||||
chr9:114633222
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.475-546C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633222 | ||||||
chr9:114633247
|
T | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-521T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633247 | ||||||
chr9:114633256
|
G | A | 12 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(9): Show | 18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.475-512G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633256 | ||||||
chr9:114633305
|
G | C | 1 | a0001c0001t0001g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.475-463G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633305 | ||||||
chr9:114633306
|
T | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-462T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633306 | ||||||
chr9:114633319
|
G | A | 6 | a0001c0002t0014g0237a0001c0002t0014g0240a0001c0002t0014g0241others(3): Show | 6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-449G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633319 | ||||||
chr9:114633381
|
C | T | 67 | a0001c0001t0003g0198a0001c0001t0004g0006a0001c0001t0004g0021others(64): Show | 90 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.475-387C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633381 | ||||||
chr9:114633404
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.475-364C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633404 | ||||||
chr9:114633412
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.475-356G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633412 | ||||||
chr9:114633464
|
G | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-304G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633464 | ||||||
chr9:114633522
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0111others(6): Show | 16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.475-246G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633522 | ||||||
chr9:114633601
|
A | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-167A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633601 | ||||||
chr9:114633610
|
A | AC | 12 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(9): Show | 18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.475-153dupC | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114633610 | |||||
chr9:114633615
|
C | T | 1 | a0001c0001t0041g0176 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.475-153C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633615 | ||||||
chr9:114633710
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.475-58C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633710 | ||||||
chr9:114633755
|
G | A | 1 | a0001c0012t0001g0123 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.475-13G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633755 | ||||||
chr9:114633899
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.585+21C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114633899 | ||||||
chr9:114633957
|
C | T | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+79C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114633957 | ||||||
chr9:114634044
|
C | A | 1 | a0001c0001t0002g0025 | 2 | NA18973.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.585+166C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634044 | ||||||
chr9:114634248
|
C | G | 2 | a0001c0001t0018g0227a0001c0001t0028g0179 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.585+370C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634248 | ||||||
chr9:114634267
|
C | T | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+389C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634267 | ||||||
chr9:114634294
|
C | G | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.585+416C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634294 | ||||||
chr9:114634377
|
T | C | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+499T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634377 | ||||||
chr9:114634394
|
G | A | 2 | a0001c0001t0016g0045a0001c0001t0016g0046 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.585+516G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634394 | ||||||
chr9:114634397
|
G | A | 33 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(30): Show | 45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.585+519G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634397 | ||||||
chr9:114634417
|
C | T | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+539C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634417 | ||||||
chr9:114634467
|
C | T | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+589C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634467 | ||||||
chr9:114634474
|
G | T | 43 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(40): Show | 61 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.585+596G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634474 | ||||||
chr9:114634537
|
C | T | 1 | a0001c0001t0017g0040 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.585+659C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634537 | ||||||
chr9:114634577
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.585+699C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634577 | ||||||
chr9:114634594
|
A | G | 7 | a0001c0001t0013g0103a0001c0001t0013g0211a0001c0001t0013g0213others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+716A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634594 | ||||||
chr9:114634683
|
C | T | 10 | a0001c0001t0013g0103a0001c0001t0013g0211a0001c0001t0013g0213others(7): Show | 10 | HG02257.hp2 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+805C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634683 | ||||||
chr9:114634724
|
T | G | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+846T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634724 | ||||||
chr9:114634732
|
G | A | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+854G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634732 | ||||||
chr9:114634775
|
G | A | 2 | a0001c0001t0018g0137a0001c0001t0018g0183 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.585+897G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634775 | ||||||
chr9:114634798
|
AC | A | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.585+921delC | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634798 | ||||||
chr9:114634800
|
A | G | 1 | a0001c0002t0014g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.585+922A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634800 | ||||||
chr9:114634864
|
C | G | 55 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(52): Show | 77 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.585+986C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634864 | ||||||
chr9:114634903
|
C | T | 2 | a0001c0001t0016g0045a0001c0001t0016g0046 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.585+1025C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634903 | ||||||
chr9:114635016
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0111a0001c0001t0001g0138others(3): Show | 12 | HG01496.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+1138A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635016 | ||||||
chr9:114635026
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.585+1148T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635026 | ||||||
chr9:114635066
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.585+1188C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635066 | ||||||
chr9:114635078
|
C | T | 12 | a0001c0001t0004g0070a0001c0001t0007g0039a0001c0001t0007g0216others(9): Show | 13 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+1200C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635078 | ||||||
chr9:114635079
|
A | G | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.585+1201A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635079 | ||||||
chr9:114635091
|
A | G | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+1213A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635091 | ||||||
chr9:114635195
|
T | A | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+1317T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635195 | ||||||
chr9:114635333
|
G | T | 1 | a0001c0015t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.585+1455G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635333 | ||||||
chr9:114635349
|
CA | C | 18 | a0001c0001t0001g0034a0001c0001t0007g0216a0001c0001t0013g0103others(15): Show | 19 | HG00642.hp1 HG02027.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+1483delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114635349 | |||||
chr9:114635349
|
CAA | C | 109 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(106): Show | 150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.585+1482_585+1483d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114635349 | |||||
chr9:114635488
|
T | C | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.586-1502T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635488 | ||||||
chr9:114635548
|
G | A | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-1442G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635548 | ||||||
chr9:114635603
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.586-1387C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635603 | ||||||
chr9:114635604
|
G | A | 3 | a0001c0001t0025g0114a0001c0001t0025g0159a0001c0001t0045g0113 | 3 | HG02109.hp1 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.586-1386G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635604 | ||||||
chr9:114635663
|
A | C | 10 | a0001c0001t0009g0026a0001c0001t0009g0086a0001c0001t0009g0096others(7): Show | 10 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.586-1327A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635663 | ||||||
chr9:114635920
|
A | T | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.586-1070A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635920 | ||||||
chr9:114635925
|
A | G | 1 | a0001c0001t0042g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.586-1065A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635925 | ||||||
chr9:114636006
|
A | G | 12 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(9): Show | 18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.586-984A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636006 | ||||||
chr9:114636211
|
G | A | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-779G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636211 | ||||||
chr9:114636281
|
A | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.586-709A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636281 | ||||||
chr9:114636363
|
G | A | 66 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(63): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.586-627G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636363 | ||||||
chr9:114636426
|
C | T | 29 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(26): Show | 41 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.586-564C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636426 | ||||||
chr9:114636484
|
C | CTTTT | 28 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0037others(25): Show | 39 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.586-504_586-501dup others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636484 | |||||
chr9:114636485
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0008g0050 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.586-501_586-500ins others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | |||||
chr9:114636485
|
T | TTTTTTTT others(17): Show |
8 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0051others(5): Show | 14 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-501_586-500ins others(24): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | |||||
chr9:114636485
|
T | TTTTTTTT others(22): Show |
2 | a0001c0001t0008g0048a0001c0001t0027g0053 | 2 | HG01928.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.586-501_586-500ins others(29): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | |||||
chr9:114636485
|
T | TTTTTTTT others(32): Show |
1 | a0001c0001t0027g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.586-501_586-500ins others(39): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | |||||
chr9:114636489
|
TC | T | 4 | a0001c0001t0003g0036a0001c0001t0003g0180a0001c0001t0003g0181others(1): Show | 5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-500delC | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636489 | ||||||
chr9:114636491
|
TTTTCTTT others(7): Show |
T | 7 | a0001c0001t0013g0103a0001c0001t0013g0211a0001c0001t0013g0213others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-484_586-471del others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636491 | |||||
chr9:114636501
|
TTTTC | T | 4 | a0001c0001t0003g0036a0001c0001t0003g0180a0001c0001t0003g0181others(1): Show | 5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-481_586-478del others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636501 | |||||
chr9:114636505
|
C | CT | 41 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0037others(38): Show | 58 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.586-482dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636505 | |||||
chr9:114636690
|
T | C | 39 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(36): Show | 51 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.586-300T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636690 | ||||||
chr9:114636823
|
G | T | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-167G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636823 | ||||||
chr9:114636865
|
A | G | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-125A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636865 | ||||||
chr9:114636962
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.586-28C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636962 | ||||||
chr9:114636983
|
C | T | 11 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.586-7C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636983 | ||||||
chr9:114637117
|
G | A | 3 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089 | 3 | HG02818.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.666+47G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637117 | ||||||
chr9:114637288
|
CT | C | 38 | a0001c0001t0001g0033a0001c0001t0001g0110a0001c0001t0002g0007others(35): Show | 63 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.666+237delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 114637288 | |||||
chr9:114637288
|
CTT | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(154): Show | 228 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.666+236_666+237del others(2): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 114637288 | |||||
chr9:114637288
|
CTTTTT | C | 44 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(41): Show | 62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.666+233_666+237del others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 114637288 | |||||
chr9:114637292
|
T | C | 1 | a0001c0001t0004g0065 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.666+222T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637292 | ||||||
chr9:114637293
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.666+223T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637293 | ||||||
chr9:114637338
|
A | G | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.666+268A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637338 | ||||||
chr9:114637378
|
C | T | 4 | a0001c0001t0003g0036a0001c0001t0003g0180a0001c0001t0003g0181others(1): Show | 5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+308C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637378 | ||||||
chr9:114637417
|
G | T | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.666+347G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637417 | ||||||
chr9:114637424
|
C | T | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.666+354C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637424 | ||||||
chr9:114637463
|
G | C | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.666+393G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637463 | ||||||
chr9:114637493
|
C | T | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.666+423C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637493 | ||||||
chr9:114637508
|
A | G | 111 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(108): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.666+438A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637508 | ||||||
chr9:114637533
|
A | G | 28 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(25): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.666+463A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637533 | ||||||
chr9:114637542
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0032 | 4 | HG00735.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+472C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637542 | ||||||
chr9:114637590
|
G | A | 6 | a0001c0002t0014g0237a0001c0002t0014g0240a0001c0002t0014g0241others(3): Show | 6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+520G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637590 | ||||||
chr9:114637690
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0111others(6): Show | 16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.666+620C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637690 | ||||||
chr9:114637734
|
G | A | 7 | a0001c0001t0013g0103a0001c0001t0013g0211a0001c0001t0013g0213others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+664G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637734 | ||||||
chr9:114637765
|
C | T | 1 | a0001c0001t0010g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.666+695C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637765 | ||||||
chr9:114638227
|
T | A | 45 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(42): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.667-317T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638227 | ||||||
chr9:114638272
|
T | C | 44 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(41): Show | 62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.667-272T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638272 | ||||||
chr9:114638326
|
G | A | 6 | a0001c0002t0014g0237a0001c0002t0014g0240a0001c0002t0014g0241others(3): Show | 6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-218G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638326 | ||||||
chr9:114638366
|
A | G | 1 | a0001c0001t0048g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.667-178A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638366 | ||||||
chr9:114638736
|
A | C | 20 | a0001c0001t0009g0026a0001c0001t0009g0086a0001c0001t0009g0096others(17): Show | 20 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.849+10A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638736 | ||||||
chr9:114638751
|
G | A | 12 | a0001c0001t0009g0026a0001c0001t0009g0086a0001c0001t0009g0096others(9): Show | 12 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+25G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638751 | ||||||
chr9:114638802
|
C | G | 10 | a0001c0001t0009g0026a0001c0001t0009g0086a0001c0001t0009g0096others(7): Show | 10 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.849+76C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638802 | ||||||
chr9:114638869
|
A | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0111others(6): Show | 16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.849+143A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638869 | ||||||
chr9:114638913
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(79): Show | 141 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.849+187G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638913 | ||||||
chr9:114639039
|
C | T | 129 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(126): Show | 170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.849+313C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639039 | ||||||
chr9:114639079
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.849+353A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639079 | ||||||
chr9:114639516
|
G | A | 50 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(47): Show | 74 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.849+790G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639516 | ||||||
chr9:114639568
|
G | A | 27 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(24): Show | 31 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.849+842G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639568 | ||||||
chr9:114639578
|
G | A | 2 | a0001c0001t0013g0211a0001c0001t0013g0213 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849+852G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639578 | ||||||
chr9:114639860
|
C | T | 2 | a0001c0001t0013g0211a0001c0001t0013g0213 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849+1134C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639860 | ||||||
chr9:114639987
|
C | T | 28 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(25): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.849+1261C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639987 | ||||||
chr9:114640005
|
C | T | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.849+1279C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640005 | ||||||
chr9:114640056
|
TA | T | 9 | a0001c0001t0001g0147a0001c0001t0001g0177a0001c0001t0002g0081others(6): Show | 9 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+1342delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114640056 | |||||
chr9:114640067
|
A | G | 14 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(11): Show | 20 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.849+1341A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640067 | ||||||
chr9:114640083
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.849+1357C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640083 | ||||||
chr9:114640114
|
CT | C | 31 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0002g0079others(28): Show | 50 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.849+1401delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114640114 | |||||
chr9:114640233
|
T | G | 1 | a0001c0001t0002g0088 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849+1507T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640233 | ||||||
chr9:114640392
|
C | T | 6 | a0001c0002t0014g0237a0001c0002t0014g0240a0001c0002t0014g0241others(3): Show | 6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+1666C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640392 | ||||||
chr9:114640632
|
T | A | 4 | a0001c0001t0003g0036a0001c0001t0003g0180a0001c0001t0003g0181others(1): Show | 5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+1906T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640632 | ||||||
chr9:114640634
|
C | A | 4 | a0001c0001t0003g0036a0001c0001t0003g0180a0001c0001t0003g0181others(1): Show | 5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+1908C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640634 | ||||||
chr9:114640639
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.849+1913C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640639 | ||||||
chr9:114640881
|
C | CT | 8 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(5): Show | 11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+2166dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114640881 | |||||
chr9:114640894
|
G | A | 4 | a0001c0001t0006g0228a0001c0001t0017g0040a0001c0001t0017g0223others(1): Show | 5 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+2168G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640894 | ||||||
chr9:114640902
|
G | A | 1 | a0001c0001t0011g0155 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.849+2176G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640902 | ||||||
chr9:114640908
|
C | T | 34 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(31): Show | 46 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.849+2182C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640908 | ||||||
chr9:114640922
|
C | G | 3 | a0001c0001t0017g0040a0001c0001t0017g0223a0001c0001t0017g0224 | 4 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+2196C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640922 | ||||||
chr9:114641170
|
C | T | 11 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(8): Show | 17 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.850-1964C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641170 | ||||||
chr9:114641171
|
C | T | 1 | a0001c0001t0009g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-1963C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641171 | ||||||
chr9:114641209
|
G | A | 1 | a0001c0001t0010g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.850-1925G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641209 | ||||||
chr9:114641229
|
T | G | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1905T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641229 | ||||||
chr9:114641240
|
A | G | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1894A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641240 | ||||||
chr9:114641362
|
C | T | 10 | a0001c0001t0009g0026a0001c0001t0009g0086a0001c0001t0009g0096others(7): Show | 10 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-1772C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641362 | ||||||
chr9:114641399
|
C | A | 1 | a0001c0001t0037g0254 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-1735C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641399 | ||||||
chr9:114641596
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-1538G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641596 | ||||||
chr9:114641637
|
A | C | 129 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(126): Show | 170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.850-1497A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641637 | ||||||
chr9:114641658
|
C | T | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1476C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641658 | ||||||
chr9:114641728
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.850-1406C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641728 | ||||||
chr9:114641793
|
A | G | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1341A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641793 | ||||||
chr9:114642012
|
G | T | 134 | a0001c0001t0003g0004a0001c0001t0003g0014a0001c0001t0003g0036others(131): Show | 175 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.850-1122G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642012 | ||||||
chr9:114642017
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.850-1117A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642017 | ||||||
chr9:114642019
|
T | C | 22 | a0001c0001t0007g0039a0001c0001t0007g0216a0001c0001t0007g0217others(19): Show | 23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.850-1115T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642019 | ||||||
chr9:114642101
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-1033G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642101 | ||||||
chr9:114642111
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.850-1023C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642111 | ||||||
chr9:114642112
|
A | G | 28 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(25): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.850-1022A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642112 | ||||||
chr9:114642240
|
C | T | 12 | a0001c0001t0008g0009a0001c0001t0008g0047a0001c0001t0008g0048others(9): Show | 18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.850-894C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642240 | ||||||
chr9:114642256
|
T | A | 8 | a0001c0001t0006g0020a0001c0001t0006g0038a0001c0001t0006g0203others(5): Show | 11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-878T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642256 | ||||||
chr9:114642271
|
C | G | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-863C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642271 | ||||||
chr9:114642340
|
C | T | 1 | a0001c0001t0037g0254 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-794C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642340 | ||||||
chr9:114642343
|
T | C | 1 | a0001c0001t0037g0254 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-791T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642343 | ||||||
chr9:114642361
|
CT | C | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-764delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114642361 | |||||
chr9:114642462
|
T | A | 1 | a0001c0001t0037g0254 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-672T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642462 | ||||||
chr9:114642499
|
A | G | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-635A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642499 | ||||||
chr9:114642545
|
C | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0147 | 2 | NA18977.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.850-589C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642545 | ||||||
chr9:114642624
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0107 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.850-510T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642624 | ||||||
chr9:114642909
|
T | C | 62 | a0001c0001t0004g0006a0001c0001t0004g0021a0001c0001t0004g0022others(59): Show | 87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-225T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642909 | ||||||
chr9:114643061
|
CCCCTGGT others(7): Show |
C | 1 | a0001c0001t0001g0148 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.850-68_850-55delGG others(12): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114643061 | |||||
chr9:114643119
|
C | T | 1 | a0001c0001t0001g0019 | 3 | NA18972.hp2 NA18986.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.850-15C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114643119 |