geneid | 54868 |
---|---|
ensemblid | ENSG00000109066.14 |
hgncid | 25984 |
symbol | TMEM104 |
name | transmembrane protein 104 |
refseq_nuc | NM_017728.4 |
refseq_prot | NP_060198.3 |
ensembl_nuc | ENST00000335464.10 |
ensembl_prot | ENSP00000334849.5 |
mane_status | MANE Select |
chr | chr17 |
start | 74776499 |
end | 74839753 |
strand | + |
ver | v1.2 |
region | chr17:74776499-74839753 |
region5000 | chr17:74771499-74844753 |
regionname0 | TMEM104_chr17_74776499_74839753 |
regionname5000 | TMEM104_chr17_74771499_74844753 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 496 | 162 | 56 | 32 | 48 | 7 | 18 | 32 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002 | 1/0 | 496 | 134 | 27 | 29 | 48 | 7 | 22 | 33 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0003 | 0/0 | 496 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0004 | 0/0 | 496 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0005 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0006 | 0/0 | 496 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0007 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0008 | 0/0 | 496 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0009 | 0/0 | 496 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1491 | 144 | 45 | 30 | 43 | 7 | 18 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0002 | 1/0 | 1491 | 113 | 17 | 21 | 45 | 7 | 22 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0003 | 0/0 | 1491 | 9 | 0 | 7 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0004 | 0/0 | 1491 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0005 | 0/0 | 1491 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0006 | 0/0 | 1491 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0007 | 0/0 | 1491 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0008 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0009 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0010 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0011 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0012 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0013 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0014 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0015 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0016 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0017 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0018 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0019 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0020 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
c0021 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3213 | 73 | 12 | 20 | 25 | 2 | 14 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0002 | 0/1 | 3213 | 67 | 11 | 18 | 23 | 3 | 11 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0003 | 0/0 | 3214 | 43 | 0 | 7 | 23 | 5 | 8 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0004 | 0/0 | 3213 | 21 | 12 | 1 | 7 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0005 | 0/0 | 3213 | 18 | 8 | 4 | 0 | 3 | 3 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0006 | 0/0 | 3214 | 17 | 0 | 5 | 8 | 1 | 3 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0007 | 0/0 | 3214 | 8 | 8 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0008 | 0/0 | 3214 | 7 | 4 | 2 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0009 | 0/0 | 3213 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0010 | 0/0 | 3213 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0011 | 0/0 | 3214 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0012 | 0/0 | 3214 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0013 | 0/0 | 3214 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0014 | 0/0 | 3214 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0015 | 0/0 | 3214 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0016 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0017 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0018 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0019 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0020 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0021 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0022 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0023 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0024 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0025 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0026 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0027 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0028 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0029 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0030 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0031 | 0/0 | 3214 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0032 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0033 | 1/0 | 3213 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0034 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0035 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0036 | 0/0 | 3213 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
t0037 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1491 | 144 | 45 | 30 | 43 | 7 | 18 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0004 | 0/0 | 1491 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0006 | 0/0 | 1491 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0008 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0010 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0011 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0012 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0017 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0021 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002 | 1/0 | 1491 | 113 | 17 | 21 | 45 | 7 | 22 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0003 | 0/0 | 1491 | 9 | 0 | 7 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0005 | 0/0 | 1491 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0007 | 0/0 | 1491 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0019 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0003c0009 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0004c0014 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0005c0015 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0006c0013 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0007c0016 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0008c0020 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0009c0018 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4703 | 11 | 2 | 0 | 7 | 0 | 2 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0002 | 0/1 | 4703 | 62 | 11 | 18 | 19 | 3 | 10 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0003 | 0/0 | 4704 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0004 | 0/0 | 4703 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0005 | 0/0 | 4703 | 18 | 8 | 4 | 0 | 3 | 3 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0006 | 0/0 | 4704 | 13 | 0 | 4 | 5 | 1 | 3 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0007 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0008 | 0/0 | 4704 | 6 | 4 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0009 | 0/0 | 4703 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0010 | 0/0 | 4703 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0014 | 0/0 | 4704 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0015 | 0/0 | 4704 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0017 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0019 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0020 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0021 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0022 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0023 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0024 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0025 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0026 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0027 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0001t0028 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0004t0011 | 0/0 | 4704 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0004t0012 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0004t0013 | 0/0 | 4704 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0006t0002 | 0/0 | 4703 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0008t0007 | 0/0 | 4704 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0010t0018 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0011t0006 | 0/0 | 4704 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0012t0006 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0017t0003 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0001c0021t0037 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0001 | 0/0 | 4703 | 49 | 7 | 13 | 16 | 2 | 11 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0003 | 0/0 | 4704 | 38 | 0 | 7 | 18 | 5 | 8 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0004 | 0/0 | 4703 | 15 | 6 | 1 | 7 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0007 | 0/0 | 4704 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0016 | 0/0 | 4703 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0017 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0029 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0030 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0031 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0033 | 1/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0035 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0002t0036 | 0/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0003t0001 | 0/0 | 4703 | 8 | 0 | 6 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0003t0032 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0005t0001 | 0/0 | 4703 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0005t0004 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0005t0007 | 0/0 | 4704 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0005t0034 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0007t0012 | 0/0 | 4704 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0002c0019t0003 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0003c0009t0002 | 0/0 | 4703 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0003c0009t0006 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0004c0014t0009 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0005c0015t0008 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0006c0013t0002 | 0/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0007c0016t0006 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0008c0020t0001 | 0/0 | 4703 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
a0009c0018t0001 | 0/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | copy fasta | chr17 | 74771499 | 74844753 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0008g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0008g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0010g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0010g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0010g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0014g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0014g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0014g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0017g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0019g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0020g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0021g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0022g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0023g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0024g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0025g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0026g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0027g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0001t0028g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0011g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0011g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0011g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0004t0013g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0006t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0006t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0006t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0008t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0008t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0010t0018g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0011t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0012t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0017t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0001c0021t0037g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0016g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0016g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0017g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0029g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0030g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0031g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0033g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0035g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0002t0036g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0003t0032g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0005t0034g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0007t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0007t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0007t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0002c0019t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0003c0009t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0003c0009t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0004c0014t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0005c0015t0008g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0006c0013t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0007c0016t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0008c0020t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
a0009c0018t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0003 | g0107 | EUR | GBR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0100 | EUR | GBR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0274 | EUR | FIN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | FIN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00423 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00438 | hp1 | a0005 | c0015 | t0008 | g0275 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00438 | hp2 | a0002 | c0019 | t0003 | g0149 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00544 | hp2 | a0002 | c0002 | t0003 | g0129 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00558 | hp1 | a0001 | c0012 | t0006 | g0208 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00639 | hp1 | a0001 | c0011 | t0006 | g0012 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0255 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00673 | hp1 | a0001 | c0001 | t0017 | g0082 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00673 | hp2 | a0002 | c0002 | t0003 | g0110 | EAS | CHS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00733 | hp2 | a0001 | c0001 | t0008 | g0229 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0148 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0194 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01069 | hp1 | a0002 | c0005 | t0034 | g0067 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01099 | hp2 | a0001 | c0001 | t0015 | g0043 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01106 | hp1 | a0001 | c0004 | t0013 | g0022 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0225 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01168 | hp2 | a0002 | c0002 | t0003 | g0122 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01175 | hp1 | a0002 | c0002 | t0003 | g0157 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0221 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01257 | hp1 | a0002 | c0002 | t0004 | g0085 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01257 | hp2 | a0001 | c0001 | t0021 | g0247 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01361 | hp1 | a0002 | c0002 | t0003 | g0147 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0253 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0143 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01433 | hp2 | a0002 | c0003 | t0001 | g0134 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01515 | hp1 | a0002 | c0002 | t0003 | g0111 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0218 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0272 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0228 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0146 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0262 | EUR | IBS | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01884 | hp1 | a0002 | c0002 | t0035 | g0075 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0049 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01891 | hp1 | a0001 | c0004 | t0011 | g0292 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01891 | hp2 | a0002 | c0002 | t0004 | g0165 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01952 | hp1 | a0002 | c0003 | t0032 | g0104 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0220 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01975 | hp1 | a0002 | c0003 | t0001 | g0089 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02004 | hp1 | a0002 | c0003 | t0001 | g0101 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02015 | hp2 | a0002 | c0002 | t0003 | g0057 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02027 | hp2 | a0001 | c0001 | t0020 | g0201 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02055 | hp2 | a0001 | c0004 | t0011 | g0287 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02071 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02145 | hp1 | a0002 | c0002 | t0007 | g0059 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0132 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02165 | hp1 | a0002 | c0002 | t0004 | g0158 | EAS | CDX | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02273 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02280 | hp1 | a0001 | c0004 | t0011 | g0291 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02293 | hp1 | a0002 | c0003 | t0001 | g0105 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0099 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02300 | hp2 | a0008 | c0020 | t0001 | g0080 | AMR | PEL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02451 | hp1 | a0002 | c0005 | t0007 | g0077 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0139 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02572 | hp1 | a0002 | c0002 | t0004 | g0060 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0232 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0294 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02615 | hp2 | a0002 | c0005 | t0007 | g0068 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02622 | hp1 | a0001 | c0001 | t0019 | g0283 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02622 | hp2 | a0002 | c0005 | t0004 | g0164 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02630 | hp1 | a0001 | c0010 | t0018 | g0288 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0295 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02698 | hp2 | a0002 | c0002 | t0003 | g0126 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02717 | hp1 | a0001 | c0004 | t0012 | g0047 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02717 | hp2 | a0001 | c0021 | t0037 | g0009 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0144 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0289 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02818 | hp2 | a0001 | c0001 | t0025 | g0222 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02886 | hp1 | a0002 | c0005 | t0001 | g0076 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02886 | hp2 | a0001 | c0001 | t0028 | g0021 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02896 | hp2 | a0001 | c0008 | t0007 | g0166 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0284 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02897 | hp2 | a0001 | c0008 | t0007 | g0162 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02922 | hp2 | a0001 | c0004 | t0013 | g0020 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02965 | hp2 | a0002 | c0007 | t0012 | g0071 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02970 | hp1 | a0001 | c0004 | t0011 | g0286 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03041 | hp2 | a0002 | c0002 | t0004 | g0065 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03098 | hp2 | a0002 | c0002 | t0004 | g0167 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03130 | hp1 | a0002 | c0007 | t0012 | g0069 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03139 | hp2 | a0002 | c0005 | t0001 | g0061 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03195 | hp1 | a0002 | c0002 | t0007 | g0074 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03195 | hp2 | a0002 | c0007 | t0012 | g0070 | AFR | ESN | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03209 | hp1 | a0001 | c0001 | t0015 | g0023 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03209 | hp2 | a0001 | c0001 | t0027 | g0206 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03225 | hp1 | a0002 | c0005 | t0007 | g0062 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03490 | hp1 | a0002 | c0002 | t0003 | g0005 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03490 | hp2 | a0006 | c0013 | t0002 | g0231 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03491 | hp1 | a0001 | c0001 | t0006 | g0244 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0005 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0195 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03688 | hp1 | a0002 | c0002 | t0036 | g0118 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0266 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0239 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0237 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0160 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0131 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04184 | hp2 | a0002 | c0002 | t0004 | g0183 | SAS | BEB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0156 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04204 | hp1 | a0009 | c0018 | t0001 | g0114 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04204 | hp2 | a0002 | c0002 | t0003 | g0079 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04228 | hp1 | a0002 | c0002 | t0031 | g0128 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18522 | hp1 | a0002 | c0002 | t0004 | g0056 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18612 | hp2 | a0001 | c0001 | t0026 | g0211 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18747 | hp1 | a0002 | c0002 | t0016 | g0097 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18906 | hp2 | a0004 | c0014 | t0009 | g0293 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18947 | hp1 | a0003 | c0009 | t0002 | g0019 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18947 | hp2 | a0003 | c0009 | t0006 | g0011 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18948 | hp1 | a0001 | c0001 | t0014 | g0013 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18948 | hp2 | a0001 | c0001 | t0022 | g0252 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18953 | hp1 | a0002 | c0002 | t0003 | g0181 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18960 | hp1 | a0002 | c0002 | t0004 | g0152 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18960 | hp2 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18971 | hp1 | a0001 | c0006 | t0002 | g0212 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18975 | hp1 | a0002 | c0002 | t0004 | g0153 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18981 | hp1 | a0002 | c0002 | t0004 | g0103 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18983 | hp1 | a0001 | c0006 | t0002 | g0205 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18983 | hp2 | a0007 | c0016 | t0006 | g0016 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18984 | hp1 | a0002 | c0002 | t0003 | g0127 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18984 | hp2 | a0001 | c0001 | t0014 | g0210 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18986 | hp1 | a0001 | c0001 | t0006 | g0209 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18986 | hp2 | a0002 | c0002 | t0017 | g0093 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18992 | hp1 | a0002 | c0002 | t0030 | g0123 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18995 | hp2 | a0001 | c0001 | t0014 | g0031 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18999 | hp1 | a0001 | c0001 | t0024 | g0200 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19002 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19003 | hp2 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19005 | hp1 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19005 | hp2 | a0001 | c0001 | t0023 | g0207 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19007 | hp1 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19009 | hp2 | a0002 | c0002 | t0003 | g0159 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19010 | hp1 | a0001 | c0017 | t0003 | g0187 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19010 | hp2 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0193 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19030 | hp2 | a0002 | c0002 | t0029 | g0163 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0290 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19056 | hp2 | a0001 | c0006 | t0002 | g0202 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19060 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19064 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19068 | hp2 | a0002 | c0002 | t0016 | g0179 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0177 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19082 | hp1 | a0002 | c0002 | t0003 | g0095 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19087 | hp1 | a0002 | c0002 | t0003 | g0145 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19087 | hp2 | a0002 | c0002 | t0004 | g0054 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19240 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA19240 | hp2 | a0002 | c0005 | t0001 | g0066 | AFR | YRI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ASW | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | ASW | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20752 | hp1 | a0002 | c0002 | t0003 | g0154 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0155 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0238 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0115 | EUR | TSI | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | GIH | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | GIH | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0108 | AMR | CLM | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0227 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG02559 | hp2 | a0001 | c0004 | t0013 | g0010 | AFR | ACB | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
HG06807 | hp2 | a0002 | c0002 | t0004 | g0172 | AFR | USA | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18955 | hp1 | a0002 | c0002 | t0004 | g0055 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA18955 | hp2 | a0002 | c0002 | t0003 | g0169 | EAS | JPT | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | LWK | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0037 | REF | REF | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0033 | g0063 | REF | REF | TMEM104_chr17_74771499_74844753 | TMEM104 | chr17 | 74771499 | 74844753 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74788793
|
G | A | 6 | a0001a0003a0004others(3): Show | 168 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
missense_variant | MODERATE | c.172G>A | p.Val58Met | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/10 | 318/4703 | 172/1491 | 58/496 | chr17 | 74788793 | ||
chr17:74790224
|
A | G | 1 | a0003 | 2 | NA18947.hp1 NA18947.hp2 |
missense_variant | MODERATE | c.274A>G | p.Thr92Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/10 | 420/4703 | 274/1491 | 92/496 | chr17 | 74790224 | ||
chr17:74790993
|
C | A | 1 | a0009 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.384C>A | p.Asp128Glu | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/10 | 530/4703 | 384/1491 | 128/496 | chr17 | 74790993 | ||
chr17:74795041
|
A | G | 1 | a0007 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.457A>G | p.Ile153Val | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/10 | 603/4703 | 457/1491 | 153/496 | chr17 | 74795041 | ||
chr17:74795600
|
C | G | 1 | a0008 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.604C>G | p.Leu202Val | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/10 | 750/4703 | 604/1491 | 202/496 | chr17 | 74795600 | ||
chr17:74836064
|
C | A | 1 | a0009 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.868C>A | p.Leu290Met | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1014/4703 | 868/1491 | 290/496 | chr17 | 74836064 | ||
chr17:74836445
|
G | A | 1 | a0006 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1249G>A | p.Asp417Asn | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1395/4703 | 1249/1491 | 417/496 | chr17 | 74836445 | ||
chr17:74836502
|
G | A | 1 | a0004 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1306G>A | p.Val436Ile | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1452/4703 | 1306/1491 | 436/496 | chr17 | 74836502 | ||
chr17:74836511
|
G | A | 1 | a0005 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1315G>A | p.Ala439Thr | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1461/4703 | 1315/1491 | 439/496 | chr17 | 74836511 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74785556
|
C | T | 1 | a0001c0021 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.120C>T | p.Ala40Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/10 | 266/4703 | 120/1491 | 40/496 | chr17 | 74785556 | ||
chr17:74788792
|
C | T | 1 | a0002c0005 | 8 | HG01069.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
synonymous_variant | LOW | c.171C>T | p.Phe57Phe | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/10 | 317/4703 | 171/1491 | 57/496 | chr17 | 74788792 | ||
chr17:74790238
|
C | T | 1 | a0001c0017 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.288C>T | p.Ser96Ser | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/10 | 434/4703 | 288/1491 | 96/496 | chr17 | 74790238 | ||
chr17:74795581
|
T | C | 1 | a0001c0010 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.585T>C | p.Thr195Thr | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/10 | 731/4703 | 585/1491 | 195/496 | chr17 | 74795581 | ||
chr17:74819842
|
C | T | 2 | a0001c0006a0002c0003 | 12 | HG01346.hp1 HG01433.hp2 HG01952.hp1 others(9): Show |
splice_region_variant&synonymous_variant | LOW | c.729C>T | p.Ile243Ile | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/10 | 875/4703 | 729/1491 | 243/496 | chr17 | 74819842 | ||
chr17:74835997
|
G | A | 1 | a0001c0011 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.801G>A | p.Leu267Leu | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 947/4703 | 801/1491 | 267/496 | chr17 | 74835997 | ||
chr17:74836186
|
C | T | 2 | a0001c0004a0002c0007 | 11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
synonymous_variant | LOW | c.990C>T | p.Arg330Arg | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1136/4703 | 990/1491 | 330/496 | chr17 | 74836186 | ||
chr17:74836225
|
G | A | 1 | a0002c0019 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.1029G>A | p.Ala343Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1175/4703 | 1029/1491 | 343/496 | chr17 | 74836225 | ||
chr17:74836366
|
G | A | 1 | a0001c0012 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1170G>A | p.Thr390Thr | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1316/4703 | 1170/1491 | 390/496 | chr17 | 74836366 | ||
chr17:74836483
|
G | A | 1 | a0001c0008 | 2 | HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1287G>A | p.Ala429Ala | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1433/4703 | 1287/1491 | 429/496 | chr17 | 74836483 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74776559
|
G | C | 30 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(27): Show | 142 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/10 | 772 | chr17 | 74776559 | |||||
chr17:74776568
|
T | C | 6 | a0001c0001t0009a0001c0001t0010a0001c0001t0019others(3): Show | 16 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-77T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/10 | 763 | chr17 | 74776568 | |||||
chr17:74777283
|
C | A | 1 | a0002c0002t0029 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/10 | 48 | chr17 | 74777283 | |||||
chr17:74836744
|
G | A | 4 | a0001c0004t0011a0001c0004t0012a0001c0004t0013others(1): Show | 11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*57G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 57 | chr17 | 74836744 | |||||
chr17:74836789
|
G | A | 13 | a0001c0001t0003a0001c0001t0006a0001c0001t0014others(10): Show | 66 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*102G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 102 | chr17 | 74836789 | |||||
chr17:74836843
|
A | AC | 27 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(24): Show | 97 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*159dupC | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 160 | INFO_REALIGN_3_PRIME | chr17 | 74836843 | ||||
chr17:74837013
|
G | T | 1 | a0002c0002t0036 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 326 | chr17 | 74837013 | |||||
chr17:74837027
|
A | G | 2 | a0001c0001t0017a0002c0002t0017 | 2 | HG00673.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*340A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 340 | chr17 | 74837027 | |||||
chr17:74837152
|
G | A | 1 | a0001c0001t0021 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 465 | chr17 | 74837152 | |||||
chr17:74837205
|
C | T | 1 | a0001c0001t0027 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 518 | chr17 | 74837205 | |||||
chr17:74837228
|
G | T | 1 | a0002c0002t0016 | 2 | NA18747.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*541G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 541 | chr17 | 74837228 | |||||
chr17:74837336
|
C | A | 1 | a0002c0003t0032 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 649 | chr17 | 74837336 | |||||
chr17:74837458
|
C | T | 1 | a0002c0002t0031 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 771 | chr17 | 74837458 | |||||
chr17:74837508
|
C | A | 1 | a0001c0021t0037 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 821 | chr17 | 74837508 | |||||
chr17:74837587
|
C | G | 1 | a0001c0001t0015 | 2 | HG01099.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*900C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 900 | chr17 | 74837587 | |||||
chr17:74837679
|
T | C | 1 | a0001c0001t0028 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 992 | chr17 | 74837679 | |||||
chr17:74837748
|
C | G | 1 | a0001c0021t0037 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1061 | chr17 | 74837748 | |||||
chr17:74837753
|
A | G | 1 | a0002c0002t0035 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1066 | chr17 | 74837753 | |||||
chr17:74837932
|
A | G | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*1245A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1245 | chr17 | 74837932 | |||||
chr17:74838019
|
C | G | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(2): Show | 44 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1332C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1332 | chr17 | 74838019 | |||||
chr17:74838234
|
T | A | 1 | a0002c0002t0030 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1547 | chr17 | 74838234 | |||||
chr17:74838250
|
C | G | 1 | a0001c0001t0026 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1563C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1563 | chr17 | 74838250 | |||||
chr17:74838446
|
A | G | 30 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(27): Show | 100 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1759A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 1759 | chr17 | 74838446 | |||||
chr17:74838729
|
G | A | 1 | a0001c0001t0014 | 3 | NA18948.hp1 NA18984.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2042G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2042 | chr17 | 74838729 | |||||
chr17:74838734
|
C | T | 1 | a0002c0005t0034 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2047C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2047 | chr17 | 74838734 | |||||
chr17:74838815
|
C | A | 28 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(25): Show | 98 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*2128C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2128 | chr17 | 74838815 | |||||
chr17:74838820
|
C | T | 1 | a0002c0002t0029 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2133C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2133 | chr17 | 74838820 | |||||
chr17:74839085
|
G | A | 1 | a0001c0001t0022 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2398G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2398 | chr17 | 74839085 | |||||
chr17:74839349
|
G | A | 1 | a0001c0001t0020 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2662G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2662 | chr17 | 74839349 | |||||
chr17:74839424
|
G | A | 1 | a0001c0001t0023 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2737G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2737 | chr17 | 74839424 | |||||
chr17:74839448
|
C | T | 2 | a0001c0001t0025a0001c0010t0018 | 2 | HG02630.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2761C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2761 | chr17 | 74839448 | |||||
chr17:74839500
|
C | G | 1 | a0001c0010t0018 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2813C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 10/10 | 2813 | chr17 | 74839500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74776582
|
T | TGGGTC | 14 | a0001c0001t0009g0284a0001c0001t0009g0285a0001c0001t0009g0289others(11): Show | 16 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-68+19_-68+23dupTC others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 74776582 | |||||
chr17:74776629
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-68+52G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776629 | ||||||
chr17:74776636
|
T | TGGGGC | 92 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(89): Show | 94 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-68+72_-68+76dupGG others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 74776636 | |||||
chr17:74776671
|
C | T | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | NA19068.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-68+94C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776671 | ||||||
chr17:74776709
|
T | C | 146 | a0001c0001t0001g0044a0001c0001t0002g0002a0001c0001t0002g0007others(143): Show | 151 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-68+132T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776709 | ||||||
chr17:74776710
|
T | G | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-68+133T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776710 | ||||||
chr17:74776908
|
C | T | 45 | a0001c0001t0002g0008a0001c0001t0002g0234a0001c0001t0002g0235others(42): Show | 46 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-68+331C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776908 | ||||||
chr17:74776971
|
G | A | 74 | a0001c0001t0002g0008a0001c0001t0002g0196a0001c0001t0002g0197others(71): Show | 75 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-67-293G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776971 | ||||||
chr17:74776976
|
A | C | 83 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0196others(80): Show | 85 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-67-288A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74776976 | ||||||
chr17:74777016
|
G | T | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-67-248G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777016 | ||||||
chr17:74777088
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-67-176C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777088 | ||||||
chr17:74777154
|
C | A | 2 | a0001c0001t0009g0284a0001c0001t0019g0283 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-67-110C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777154 | ||||||
chr17:74777194
|
A | G | 73 | a0001c0001t0002g0008a0001c0001t0002g0196a0001c0001t0002g0197others(70): Show | 74 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-67-70A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777194 | ||||||
chr17:74777248
|
G | A | 112 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(109): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-67-16G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 1/9 | chr17 | 74777248 | ||||||
chr17:74777499
|
T | C | 11 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(8): Show | 11 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+124T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777499 | ||||||
chr17:74777655
|
C | A | 146 | a0001c0001t0001g0044a0001c0001t0002g0002a0001c0001t0002g0007others(143): Show | 151 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.45+280C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777655 | ||||||
chr17:74777745
|
C | A | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.45+370C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777745 | ||||||
chr17:74777772
|
A | G | 1 | a0002c0002t0001g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+397A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777772 | ||||||
chr17:74777846
|
G | A | 3 | a0002c0002t0004g0053a0002c0002t0004g0054a0002c0002t0004g0055 | 3 | NA18955.hp1 NA19003.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.45+471G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777846 | ||||||
chr17:74777850
|
G | A | 11 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(8): Show | 11 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+475G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777850 | ||||||
chr17:74777874
|
G | A | 146 | a0001c0001t0001g0044a0001c0001t0002g0002a0001c0001t0002g0007others(143): Show | 151 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.45+499G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777874 | ||||||
chr17:74777989
|
T | C | 121 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(118): Show | 124 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.45+614T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74777989 | ||||||
chr17:74778036
|
G | A | 112 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(109): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.45+661G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778036 | ||||||
chr17:74778043
|
TC | T | 3 | a0001c0001t0002g0223a0001c0001t0005g0224a0001c0001t0008g0225 | 3 | HG00738.hp1 HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.45+669delC | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778043 | ||||||
chr17:74778073
|
TA | T | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+699delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778073 | ||||||
chr17:74778101
|
G | A | 1 | a0002c0002t0004g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+726G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778101 | ||||||
chr17:74778212
|
C | T | 1 | a0002c0002t0001g0191 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45+837C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778212 | ||||||
chr17:74778362
|
C | T | 2 | a0001c0001t0002g0042a0001c0001t0015g0043 | 2 | HG01099.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.45+987C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778362 | ||||||
chr17:74778419
|
G | A | 112 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(109): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.45+1044G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778419 | ||||||
chr17:74778421
|
A | G | 22 | a0001c0001t0001g0044a0001c0001t0002g0034a0001c0001t0002g0035others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+1046A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778421 | ||||||
chr17:74778538
|
C | G | 83 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0196others(80): Show | 85 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.45+1163C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778538 | ||||||
chr17:74778599
|
C | G | 158 | a0001c0001t0001g0044a0001c0001t0001g0184a0001c0001t0001g0185others(155): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.45+1224C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778599 | ||||||
chr17:74778639
|
C | CT | 28 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0278others(25): Show | 28 | HG00408.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+1290dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | |||||
chr17:74778639
|
C | CTT | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+1289_45+1290dup others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | |||||
chr17:74778639
|
CT | C | 13 | a0001c0001t0001g0044a0001c0001t0002g0030a0001c0001t0002g0041others(10): Show | 13 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+1290delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | |||||
chr17:74778639
|
CTT | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(40): Show | 44 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.45+1289_45+1290del others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | |||||
chr17:74778639
|
CTTT | C | 74 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0196others(71): Show | 76 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.45+1288_45+1290del others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778639 | |||||
chr17:74778782
|
CCCCACCC others(1): Show |
C | 22 | a0001c0001t0001g0044a0001c0001t0002g0034a0001c0001t0002g0035others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+1412_45+1419del others(8): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74778782 | |||||
chr17:74778960
|
A | G | 146 | a0001c0001t0001g0044a0001c0001t0002g0002a0001c0001t0002g0007others(143): Show | 151 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.45+1585A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74778960 | ||||||
chr17:74779201
|
C | G | 112 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(109): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.45+1826C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779201 | ||||||
chr17:74779219
|
G | A | 146 | a0001c0001t0001g0044a0001c0001t0002g0002a0001c0001t0002g0007others(143): Show | 151 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.45+1844G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779219 | ||||||
chr17:74779279
|
C | T | 1 | a0002c0002t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.45+1904C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779279 | ||||||
chr17:74779295
|
C | T | 2 | a0001c0001t0010g0294a0001c0001t0010g0295 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.45+1920C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779295 | ||||||
chr17:74779375
|
G | C | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.45+2000G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779375 | ||||||
chr17:74779497
|
G | A | 1 | a0002c0002t0001g0191 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45+2122G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779497 | ||||||
chr17:74779529
|
G | A | 1 | a0003c0009t0006g0011 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.45+2154G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779529 | ||||||
chr17:74779546
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+2171G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779546 | ||||||
chr17:74779654
|
C | T | 1 | a0002c0002t0003g0160 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.45+2279C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779654 | ||||||
chr17:74779772
|
A | G | 121 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(118): Show | 125 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.45+2397A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779772 | ||||||
chr17:74779883
|
A | C | 2 | a0001c0001t0009g0284a0001c0001t0019g0283 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+2508A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74779883 | ||||||
chr17:74780134
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.45+2759C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780134 | ||||||
chr17:74780372
|
G | A | 9 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(6): Show | 9 | HG01243.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+2997G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780372 | ||||||
chr17:74780549
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.45+3174G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780549 | ||||||
chr17:74780631
|
T | C | 9 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(6): Show | 9 | HG01243.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+3256T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780631 | ||||||
chr17:74780867
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.45+3492T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780867 | ||||||
chr17:74780928
|
A | G | 1 | a0002c0005t0007g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+3553A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74780928 | ||||||
chr17:74781286
|
T | G | 1 | a0001c0011t0006g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45+3911T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781286 | ||||||
chr17:74781658
|
G | T | 1 | a0002c0002t0004g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.46-3824G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781658 | ||||||
chr17:74781666
|
C | G | 1 | a0001c0001t0002g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.46-3816C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781666 | ||||||
chr17:74781668
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.46-3814C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781668 | ||||||
chr17:74781748
|
G | C | 1 | a0002c0002t0001g0078 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.46-3734G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781748 | ||||||
chr17:74781867
|
C | T | 1 | a0002c0002t0003g0159 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.46-3615C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781867 | ||||||
chr17:74781906
|
G | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-3576G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74781906 | ||||||
chr17:74782073
|
C | T | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-3409C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782073 | ||||||
chr17:74782109
|
C | T | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-3373C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782109 | ||||||
chr17:74782213
|
G | T | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-3269G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782213 | ||||||
chr17:74782456
|
T | G | 2 | a0002c0002t0003g0079a0008c0020t0001g0080 | 2 | HG02300.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.46-3026T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782456 | ||||||
chr17:74782462
|
G | A | 1 | a0002c0002t0001g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46-3020G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782462 | ||||||
chr17:74782476
|
G | A | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-3006G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782476 | ||||||
chr17:74782498
|
G | A | 11 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(8): Show | 11 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-2984G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782498 | ||||||
chr17:74782665
|
G | A | 1 | a0002c0002t0004g0053 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.46-2817G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782665 | ||||||
chr17:74782822
|
G | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-2660G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74782822 | ||||||
chr17:74783117
|
G | A | 11 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(8): Show | 11 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-2365G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783117 | ||||||
chr17:74783404
|
C | T | 1 | a0002c0002t0004g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.46-2078C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783404 | ||||||
chr17:74783721
|
C | CT | 45 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0279others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.46-1734dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | |||||
chr17:74783721
|
CT | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(26): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.46-1734delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | |||||
chr17:74783721
|
CTTT | C | 24 | a0001c0001t0001g0044a0001c0001t0002g0034a0001c0001t0002g0035others(21): Show | 26 | HG01099.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.46-1736_46-1734del others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | |||||
chr17:74783721
|
CTTTT | C | 7 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0048others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1737_46-1734del others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | |||||
chr17:74783721
|
CTTTTTTT others(2): Show |
C | 85 | a0001c0001t0001g0083a0001c0001t0002g0007a0001c0001t0002g0008others(82): Show | 87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.46-1742_46-1734del others(9): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | |||||
chr17:74783721
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-1744_46-1734del others(11): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74783721 | |||||
chr17:74783729
|
T | C | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-1753T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783729 | ||||||
chr17:74783734
|
T | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(20): Show | 24 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-1748T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783734 | ||||||
chr17:74783762
|
G | T | 7 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1720G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783762 | ||||||
chr17:74783791
|
C | T | 2 | a0001c0001t0009g0284a0001c0001t0019g0283 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-1691C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783791 | ||||||
chr17:74783930
|
T | C | 17 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(14): Show | 19 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-1552T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783930 | ||||||
chr17:74783986
|
C | T | 22 | a0001c0001t0001g0044a0001c0001t0002g0034a0001c0001t0002g0035others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.46-1496C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74783986 | ||||||
chr17:74784023
|
G | A | 22 | a0001c0001t0001g0044a0001c0001t0002g0034a0001c0001t0002g0035others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.46-1459G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784023 | ||||||
chr17:74784038
|
T | TA | 112 | a0001c0001t0001g0083a0001c0001t0002g0002a0001c0001t0002g0007others(109): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.46-1431dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74784038 | |||||
chr17:74784052
|
C | A | 6 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(3): Show | 6 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-1430C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784052 | ||||||
chr17:74784266
|
A | G | 1 | a0002c0002t0003g0160 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.46-1216A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784266 | ||||||
chr17:74784352
|
G | A | 86 | a0001c0001t0001g0083a0001c0001t0002g0007a0001c0001t0002g0008others(83): Show | 88 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.46-1130G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784352 | ||||||
chr17:74784613
|
G | A | 1 | a0001c0001t0006g0236 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.46-869G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784613 | ||||||
chr17:74784672
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46-810A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784672 | ||||||
chr17:74784680
|
C | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-802C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784680 | ||||||
chr17:74784691
|
T | C | 161 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(158): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.46-791T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784691 | ||||||
chr17:74784788
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0005g0224a0001c0001t0008g0225 | 3 | HG00738.hp1 HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.46-694C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784788 | ||||||
chr17:74784836
|
G | T | 1 | a0002c0002t0003g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.46-646G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784836 | ||||||
chr17:74784959
|
T | TC | 5 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-523_46-522insC | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784959 | ||||||
chr17:74784965
|
T | A | 5 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-517T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784965 | ||||||
chr17:74784965
|
T | TA | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-517_46-516insA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784965 | ||||||
chr17:74784966
|
T | A | 17 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(14): Show | 19 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-516T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74784966 | ||||||
chr17:74784966
|
T | TA | 142 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(139): Show | 145 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-511dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 74784966 | |||||
chr17:74785044
|
A | G | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.46-438A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785044 | ||||||
chr17:74785069
|
A | G | 151 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0002g0002others(148): Show | 156 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.46-413A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785069 | ||||||
chr17:74785148
|
G | T | 2 | a0002c0002t0003g0129a0002c0002t0003g0177 | 2 | HG00544.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.46-334G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785148 | ||||||
chr17:74785153
|
C | G | 144 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(141): Show | 147 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.46-329C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785153 | ||||||
chr17:74785288
|
G | A | 1 | a0002c0002t0004g0085 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.46-194G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 2/9 | chr17 | 74785288 | ||||||
chr17:74785642
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.167+39T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785642 | ||||||
chr17:74785655
|
A | T | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.167+52A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785655 | ||||||
chr17:74785673
|
G | A | 149 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0002g0002others(146): Show | 154 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.167+70G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785673 | ||||||
chr17:74785722
|
G | A | 2 | a0001c0001t0004g0045a0001c0001t0004g0050 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.167+119G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785722 | ||||||
chr17:74785883
|
C | A | 2 | a0001c0001t0009g0284a0001c0001t0019g0283 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.167+280C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785883 | ||||||
chr17:74785885
|
C | G | 10 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+282C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74785885 | ||||||
chr17:74786077
|
T | C | 127 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(124): Show | 130 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.167+474T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786077 | ||||||
chr17:74786098
|
C | T | 1 | a0002c0002t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.167+495C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786098 | ||||||
chr17:74786229
|
G | A | 4 | a0001c0008t0007g0162a0001c0008t0007g0166a0002c0002t0001g0058others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+626G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786229 | ||||||
chr17:74786260
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.167+657C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786260 | ||||||
chr17:74786337
|
T | A | 98 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(95): Show | 100 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.167+734T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786337 | ||||||
chr17:74786342
|
AGGAGCAC others(2): Show |
A | 89 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(86): Show | 90 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.167+743_167+751del others(9): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74786342 | |||||
chr17:74786362
|
C | T | 89 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(86): Show | 90 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.167+759C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786362 | ||||||
chr17:74786566
|
G | A | 11 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.167+963G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786566 | ||||||
chr17:74786587
|
C | G | 149 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0002g0002others(146): Show | 154 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.167+984C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786587 | ||||||
chr17:74786818
|
G | T | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.167+1215G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786818 | ||||||
chr17:74786999
|
G | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.167+1396G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74786999 | ||||||
chr17:74787012
|
GTC | G | 3 | a0002c0007t0012g0069a0002c0007t0012g0070a0002c0007t0012g0071 | 3 | HG02965.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.167+1413_167+1414d others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787012 | |||||
chr17:74787128
|
C | A | 8 | a0001c0001t0002g0235a0001c0001t0002g0240a0001c0001t0002g0241others(5): Show | 8 | HG01074.hp2 HG02258.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+1525C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787128 | ||||||
chr17:74787238
|
C | T | 2 | a0001c0001t0010g0294a0001c0001t0010g0295 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.168-1551C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787238 | ||||||
chr17:74787246
|
T | C | 161 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(158): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.168-1543T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787246 | ||||||
chr17:74787297
|
AGTCTGCT others(94): Show |
A | 11 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(8): Show | 11 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-1490_168-1390d others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787297 | |||||
chr17:74787344
|
C | T | 2 | a0002c0002t0003g0156a0002c0002t0031g0128 | 2 | HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.168-1445C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787344 | ||||||
chr17:74787349
|
G | A | 6 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198others(3): Show | 6 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-1440G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787349 | ||||||
chr17:74787361
|
A | G | 150 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(147): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.168-1428A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787361 | ||||||
chr17:74787394
|
A | G | 150 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(147): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.168-1395A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787394 | ||||||
chr17:74787426
|
T | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-1363T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787426 | ||||||
chr17:74787479
|
G | A | 22 | a0001c0001t0001g0044a0001c0001t0002g0034a0001c0001t0002g0035others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.168-1310G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787479 | ||||||
chr17:74787592
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.168-1197G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787592 | ||||||
chr17:74787607
|
C | T | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168-1182C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787607 | ||||||
chr17:74787623
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1166C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787623 | ||||||
chr17:74787628
|
CA | C | 159 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(156): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.168-1146delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787628 | |||||
chr17:74787630
|
A | C | 22 | a0001c0001t0001g0044a0001c0001t0002g0034a0001c0001t0002g0035others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.168-1159A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787630 | ||||||
chr17:74787659
|
A | C | 161 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(158): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.168-1130A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787659 | ||||||
chr17:74787682
|
G | A | 11 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(8): Show | 11 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-1107G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787682 | ||||||
chr17:74787797
|
C | CT | 104 | a0002c0002t0001g0006a0002c0002t0001g0078a0002c0002t0001g0084others(101): Show | 108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.168-978dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787797 | |||||
chr17:74787797
|
CT | C | 160 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(157): Show | 165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.168-978delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 74787797 | |||||
chr17:74787816
|
C | T | 1 | a0002c0002t0003g0160 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.168-973C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787816 | ||||||
chr17:74787856
|
C | T | 161 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(158): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.168-933C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787856 | ||||||
chr17:74787985
|
G | A | 1 | a0002c0002t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.168-804G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787985 | ||||||
chr17:74787985
|
G | T | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-804G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74787985 | ||||||
chr17:74788029
|
T | G | 9 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(6): Show | 9 | HG01243.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.168-760T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788029 | ||||||
chr17:74788315
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.168-474G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788315 | ||||||
chr17:74788324
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.168-465G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788324 | ||||||
chr17:74788491
|
A | G | 161 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(158): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.168-298A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788491 | ||||||
chr17:74788510
|
C | T | 88 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(85): Show | 89 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.168-279C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788510 | ||||||
chr17:74788566
|
A | C | 1 | a0002c0005t0001g0076 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.168-223A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788566 | ||||||
chr17:74788580
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.168-209C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788580 | ||||||
chr17:74788588
|
G | A | 1 | a0004c0014t0009g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.168-201G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788588 | ||||||
chr17:74788596
|
G | A | 1 | a0001c0001t0024g0200 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.168-193G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788596 | ||||||
chr17:74788705
|
G | T | 1 | a0002c0002t0004g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.168-84G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788705 | ||||||
chr17:74788718
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-71A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788718 | ||||||
chr17:74788751
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.168-38C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 3/9 | chr17 | 74788751 | ||||||
chr17:74788929
|
C | T | 1 | a0002c0005t0007g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249+59C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74788929 | ||||||
chr17:74788933
|
C | T | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.249+63C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74788933 | ||||||
chr17:74788958
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.249+88A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74788958 | ||||||
chr17:74789256
|
G | A | 10 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+386G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789256 | ||||||
chr17:74789258
|
G | A | 2 | a0002c0003t0001g0088a0002c0003t0001g0089 | 2 | HG01975.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.249+388G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789258 | ||||||
chr17:74789394
|
ATGATG | A | 5 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+527_249+531del others(5): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789394 | |||||
chr17:74789447
|
G | A | 2 | a0001c0001t0009g0284a0001c0001t0019g0283 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.249+577G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789447 | ||||||
chr17:74789543
|
C | CA | 14 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(11): Show | 16 | HG01175.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.250-639dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789543 | |||||
chr17:74789543
|
CA | C | 136 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0002g0002others(133): Show | 139 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.250-639delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789543 | |||||
chr17:74789738
|
G | A | 1 | a0002c0002t0004g0054 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.250-462G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789738 | ||||||
chr17:74789809
|
C | T | 2 | a0002c0005t0001g0066a0002c0005t0001g0076 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.250-391C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789809 | ||||||
chr17:74789845
|
C | CA | 23 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0279others(20): Show | 24 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.250-333dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789845 | |||||
chr17:74789845
|
CA | C | 13 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(10): Show | 13 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-333delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789845 | |||||
chr17:74789845
|
CAA | C | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-334_250-333del others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789845 | |||||
chr17:74789890
|
T | C | 161 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(158): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.250-310T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789890 | ||||||
chr17:74789917
|
C | CT | 11 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0037others(8): Show | 11 | HG01099.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-274dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789917 | |||||
chr17:74789940
|
C | CT | 3 | a0001c0001t0002g0024a0001c0001t0002g0215a0001c0001t0004g0052 | 3 | HG02145.hp2 HG03579.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.250-254dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789940 | |||||
chr17:74789947
|
G | T | 139 | a0001c0001t0001g0083a0001c0001t0002g0002a0001c0001t0002g0007others(136): Show | 144 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.250-253G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789947 | ||||||
chr17:74789955
|
G | T | 22 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(19): Show | 24 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.250-245G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74789955 | ||||||
chr17:74789963
|
GT | G | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-230delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 74789963 | |||||
chr17:74790018
|
A | G | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-182A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74790018 | ||||||
chr17:74790079
|
A | G | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.250-121A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 4/9 | chr17 | 74790079 | ||||||
chr17:74790334
|
C | T | 1 | a0001c0001t0002g0268 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.346+38C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790334 | ||||||
chr17:74790384
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.346+88C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790384 | ||||||
chr17:74790385
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.346+89G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790385 | ||||||
chr17:74790472
|
G | T | 106 | a0002c0002t0001g0006a0002c0002t0001g0078a0002c0002t0001g0084others(103): Show | 110 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.346+176G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790472 | ||||||
chr17:74790609
|
G | A | 1 | a0001c0004t0013g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.346+313G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790609 | ||||||
chr17:74790694
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.347-262T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790694 | ||||||
chr17:74790770
|
C | CT | 18 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0034others(15): Show | 18 | HG00738.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.347-184dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 74790770 | |||||
chr17:74790772
|
T | TTA | 3 | a0001c0001t0002g0030a0001c0001t0005g0033a0007c0016t0006g0016 | 3 | HG02486.hp2 NA18983.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.347-184_347-183ins others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790772 | ||||||
chr17:74790772
|
TA | T | 31 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0002g0199others(28): Show | 33 | HG00323.hp1 HG00323.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-164delA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 74790772 | |||||
chr17:74790773
|
A | T | 118 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(115): Show | 121 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.347-183A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790773 | ||||||
chr17:74790774
|
A | T | 20 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0002g0199others(17): Show | 22 | HG00323.hp1 HG00323.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.347-182A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790774 | ||||||
chr17:74790775
|
A | T | 1 | a0001c0001t0009g0285 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-181A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790775 | ||||||
chr17:74790776
|
A | T | 1 | a0001c0006t0002g0205 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.347-180A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790776 | ||||||
chr17:74790891
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.347-65C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 5/9 | chr17 | 74790891 | ||||||
chr17:74791254
|
T | TAGCGGAA others(89): Show |
5 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+225_427+320dup others(96): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791254 | |||||
chr17:74791324
|
G | GGGTCAGG others(25): Show |
1 | a0002c0002t0003g0169 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.427+317_427+348dup others(32): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791324 | |||||
chr17:74791353
|
C | T | 13 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(10): Show | 15 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+317C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791353 | ||||||
chr17:74791354
|
G | A | 1 | a0002c0003t0001g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.427+318G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791354 | ||||||
chr17:74791355
|
G | A | 13 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(10): Show | 15 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+319G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791355 | ||||||
chr17:74791356
|
A | AAGTCAGG others(121): Show |
23 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(20): Show | 24 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.427+320_427+321ins others(128): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791356 | ||||||
chr17:74791356
|
A | AGGTCAGG others(25): Show |
1 | a0002c0002t0029g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.427+322_427+353dup others(32): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791356 | |||||
chr17:74791356
|
A | G | 13 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(10): Show | 15 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+320A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791356 | ||||||
chr17:74791358
|
GTCAGGAA others(25): Show |
G | 9 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.427+354_427+385del others(32): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74791358 | |||||
chr17:74791385
|
T | C | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+349T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791385 | ||||||
chr17:74791387
|
A | G | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+351A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791387 | ||||||
chr17:74791388
|
G | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+352G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791388 | ||||||
chr17:74791390
|
T | G | 152 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(149): Show | 157 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.427+354T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791390 | ||||||
chr17:74791459
|
G | T | 1 | a0001c0001t0002g0234 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.427+423G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791459 | ||||||
chr17:74791545
|
T | C | 98 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(95): Show | 100 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.427+509T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791545 | ||||||
chr17:74791600
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.427+564C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791600 | ||||||
chr17:74791680
|
C | A | 1 | a0002c0002t0004g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.427+644C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791680 | ||||||
chr17:74791875
|
G | A | 9 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0030others(6): Show | 9 | HG00738.hp2 HG01106.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+839G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791875 | ||||||
chr17:74791893
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0004g0045a0001c0001t0004g0046others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+857T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791893 | ||||||
chr17:74791912
|
C | T | 3 | a0002c0002t0001g0121a0002c0002t0003g0122a0002c0002t0003g0126 | 3 | HG01168.hp2 HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.427+876C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791912 | ||||||
chr17:74791959
|
A | C | 3 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0050 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.427+923A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74791959 | ||||||
chr17:74792033
|
C | G | 1 | a0001c0001t0002g0214 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.427+997C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792033 | ||||||
chr17:74792103
|
G | A | 2 | a0001c0001t0009g0284a0001c0001t0019g0283 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.427+1067G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792103 | ||||||
chr17:74792105
|
C | T | 5 | a0001c0001t0002g0245a0001c0001t0002g0267a0001c0001t0002g0268others(2): Show | 5 | HG00323.hp1 HG02280.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+1069C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792105 | ||||||
chr17:74792123
|
G | A | 10 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0027others(7): Show | 11 | HG00639.hp1 HG01106.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.427+1087G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792123 | ||||||
chr17:74792230
|
C | T | 87 | a0001c0001t0001g0083a0001c0001t0002g0007a0001c0001t0002g0008others(84): Show | 89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.427+1194C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792230 | ||||||
chr17:74792392
|
A | G | 2 | a0002c0002t0001g0151a0002c0002t0003g0120 | 2 | HG00423.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.427+1356A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792392 | ||||||
chr17:74792494
|
C | T | 2 | a0002c0002t0001g0150a0002c0002t0001g0155 | 2 | HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.427+1458C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792494 | ||||||
chr17:74792568
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+1532G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792568 | ||||||
chr17:74792605
|
G | A | 1 | a0002c0002t0001g0090 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.427+1569G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792605 | ||||||
chr17:74792607
|
G | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+1571G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792607 | ||||||
chr17:74792635
|
C | G | 2 | a0001c0001t0005g0224a0001c0001t0008g0225 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.427+1599C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792635 | ||||||
chr17:74792635
|
C | T | 1 | a0002c0002t0029g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.427+1599C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792635 | ||||||
chr17:74792665
|
G | C | 86 | a0001c0001t0001g0083a0001c0001t0002g0007a0001c0001t0002g0008others(83): Show | 88 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.427+1629G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792665 | ||||||
chr17:74792732
|
T | A | 1 | a0002c0002t0003g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.427+1696T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792732 | ||||||
chr17:74792752
|
C | T | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.427+1716C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792752 | ||||||
chr17:74792907
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.427+1871G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792907 | ||||||
chr17:74792999
|
C | T | 1 | a0002c0002t0004g0085 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.427+1963C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74792999 | ||||||
chr17:74793094
|
C | G | 2 | a0002c0002t0001g0119a0002c0002t0036g0118 | 2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.428-1918C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793094 | ||||||
chr17:74793173
|
C | T | 29 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0018others(26): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.428-1839C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793173 | ||||||
chr17:74793444
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-1568G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793444 | ||||||
chr17:74793663
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.428-1349C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793663 | ||||||
chr17:74793676
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-1336G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793676 | ||||||
chr17:74793738
|
C | G | 1 | a0002c0019t0003g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.428-1274C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793738 | ||||||
chr17:74793749
|
C | T | 2 | a0002c0002t0001g0168a0002c0002t0003g0175 | 2 | NA18994.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.428-1263C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793749 | ||||||
chr17:74793877
|
C | T | 2 | a0002c0005t0007g0068a0002c0005t0034g0067 | 2 | HG01069.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.428-1135C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74793877 | ||||||
chr17:74794158
|
C | G | 1 | a0002c0002t0001g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.428-854C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794158 | ||||||
chr17:74794191
|
ATTC | A | 4 | a0001c0001t0001g0044a0001c0001t0004g0048a0001c0001t0007g0049others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-816_428-814del others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 74794191 | |||||
chr17:74794234
|
T | C | 291 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(288): Show | 300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.428-778T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794234 | ||||||
chr17:74794247
|
C | G | 3 | a0001c0001t0010g0001a0001c0004t0011g0291a0001c0004t0011g0292 | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-765C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794247 | ||||||
chr17:74794327
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-685G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794327 | ||||||
chr17:74794399
|
G | A | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-613G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794399 | ||||||
chr17:74794401
|
A | G | 1 | a0001c0001t0007g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.428-611A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794401 | ||||||
chr17:74794424
|
G | A | 111 | a0001c0001t0001g0083a0001c0001t0002g0002a0001c0001t0002g0007others(108): Show | 114 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.428-588G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794424 | ||||||
chr17:74794494
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.428-518G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794494 | ||||||
chr17:74794544
|
C | T | 5 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-468C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794544 | ||||||
chr17:74794603
|
T | G | 1 | a0002c0002t0004g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.428-409T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794603 | ||||||
chr17:74794604
|
AGAGCCCG others(27): Show |
A | 1 | a0002c0002t0004g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.428-407_428-374del others(34): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794604 | ||||||
chr17:74794625
|
C | G | 12 | a0001c0001t0009g0285a0001c0001t0009g0289a0001c0001t0009g0290others(9): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-387C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794625 | ||||||
chr17:74794698
|
A | T | 14 | a0001c0001t0004g0052a0001c0001t0009g0285a0001c0001t0009g0289others(11): Show | 16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.428-314A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794698 | ||||||
chr17:74794780
|
C | T | 2 | a0002c0005t0001g0066a0002c0005t0001g0076 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.428-232C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794780 | ||||||
chr17:74794797
|
T | A | 5 | a0001c0001t0002g0223a0001c0001t0005g0029a0001c0001t0005g0224others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-215T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794797 | ||||||
chr17:74794949
|
A | AG | 172 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0186others(169): Show | 177 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.428-63_428-62insG | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794949 | ||||||
chr17:74794950
|
A | G | 8 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0189others(5): Show | 8 | HG00408.hp1 HG01069.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-62A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 6/9 | chr17 | 74794950 | ||||||
chr17:74795125
|
T | C | 1 | a0001c0001t0027g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.527+14T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795125 | ||||||
chr17:74795127
|
G | A | 216 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0185others(213): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.527+16G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795127 | ||||||
chr17:74795470
|
A | G | 3 | a0001c0001t0006g0203a0001c0001t0017g0082a0001c0001t0020g0201 | 3 | HG00673.hp1 HG02027.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.528-54A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795470 | ||||||
chr17:74795479
|
A | G | 212 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(209): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.528-45A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 7/9 | chr17 | 74795479 | ||||||
chr17:74795738
|
A | G | 1 | a0002c0005t0007g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+106A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795738 | ||||||
chr17:74795763
|
A | G | 1 | a0002c0005t0007g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+131A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795763 | ||||||
chr17:74795799
|
G | A | 1 | a0002c0002t0003g0127 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.636+167G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795799 | ||||||
chr17:74795932
|
G | A | 93 | a0001c0001t0001g0083a0001c0001t0001g0277a0001c0001t0002g0034others(90): Show | 95 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.636+300G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74795932 | ||||||
chr17:74796029
|
G | A | 1 | a0002c0002t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.636+397G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796029 | ||||||
chr17:74796045
|
G | A | 66 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0002g0007others(63): Show | 69 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.636+413G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796045 | ||||||
chr17:74796104
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0189 | 2 | HG00408.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.636+472C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796104 | ||||||
chr17:74796149
|
G | A | 2 | a0001c0001t0002g0256a0001c0001t0003g0276 | 2 | HG01256.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.636+517G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796149 | ||||||
chr17:74796387
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.636+755G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796387 | ||||||
chr17:74796614
|
A | G | 80 | a0001c0001t0001g0277a0001c0001t0002g0028a0001c0001t0002g0034others(77): Show | 82 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.636+982A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796614 | ||||||
chr17:74796806
|
G | A | 1 | a0002c0002t0035g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.636+1174G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796806 | ||||||
chr17:74796976
|
G | A | 1 | a0002c0005t0007g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+1344G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74796976 | ||||||
chr17:74797130
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.636+1498G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797130 | ||||||
chr17:74797259
|
C | T | 4 | a0001c0001t0002g0034a0001c0001t0002g0041a0001c0001t0005g0025others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+1627C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797259 | ||||||
chr17:74797422
|
A | T | 3 | a0001c0021t0037g0009a0002c0002t0001g0058a0002c0002t0004g0167 | 3 | HG02717.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.636+1790A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797422 | ||||||
chr17:74797429
|
G | A | 1 | a0002c0002t0004g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.636+1797G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797429 | ||||||
chr17:74797529
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.636+1897G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797529 | ||||||
chr17:74797592
|
G | T | 1 | a0001c0001t0002g0037 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.636+1960G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797592 | ||||||
chr17:74797594
|
A | G | 109 | a0001c0001t0001g0277a0001c0001t0002g0028a0001c0001t0002g0034others(106): Show | 111 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.636+1962A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797594 | ||||||
chr17:74797640
|
G | A | 1 | a0009c0018t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.636+2008G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797640 | ||||||
chr17:74797644
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.636+2012G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797644 | ||||||
chr17:74797819
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.636+2187C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797819 | ||||||
chr17:74797859
|
C | G | 1 | a0001c0001t0008g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.636+2227C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797859 | ||||||
chr17:74797862
|
G | A | 1 | a0002c0002t0004g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.636+2230G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797862 | ||||||
chr17:74797974
|
T | G | 2 | a0001c0001t0023g0207a0001c0006t0002g0202 | 2 | NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.636+2342T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74797974 | ||||||
chr17:74798079
|
G | A | 2 | a0001c0001t0019g0283a0002c0002t0004g0060 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.636+2447G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798079 | ||||||
chr17:74798235
|
A | G | 78 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(75): Show | 80 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.636+2603A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798235 | ||||||
chr17:74798518
|
C | T | 8 | a0001c0001t0008g0015a0001c0001t0015g0023a0001c0001t0015g0043others(5): Show | 8 | HG01099.hp2 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+2886C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798518 | ||||||
chr17:74798534
|
C | A | 3 | a0001c0001t0009g0289a0001c0001t0009g0290a0004c0014t0009g0293 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.636+2902C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798534 | ||||||
chr17:74798579
|
G | A | 1 | a0002c0002t0035g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.636+2947G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74798579 | ||||||
chr17:74798883
|
AAC | A | 8 | a0001c0001t0002g0034a0001c0001t0002g0041a0001c0001t0005g0025others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+3255_636+3256d others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74798883 | |||||
chr17:74799030
|
TC | T | 294 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(291): Show | 303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.636+3403delC | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74799030 | |||||
chr17:74799059
|
A | G | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+3427A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799059 | ||||||
chr17:74799179
|
G | A | 1 | a0001c0001t0005g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.636+3547G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799179 | ||||||
chr17:74799190
|
GCTGAAAG others(3): Show |
G | 1 | a0001c0001t0027g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636+3571_636+3580d others(12): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74799190 | |||||
chr17:74799326
|
C | T | 14 | a0001c0001t0004g0045a0001c0001t0004g0048a0001c0001t0004g0050others(11): Show | 14 | HG01099.hp2 HG02055.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.636+3694C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799326 | ||||||
chr17:74799332
|
T | G | 4 | a0002c0002t0004g0053a0002c0002t0004g0054a0002c0002t0004g0055others(1): Show | 4 | NA18955.hp1 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+3700T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799332 | ||||||
chr17:74799634
|
C | T | 3 | a0001c0001t0004g0045a0001c0001t0004g0048a0001c0001t0004g0050 | 3 | HG03486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.636+4002C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799634 | ||||||
chr17:74799775
|
T | C | 1 | a0002c0002t0004g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.636+4143T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799775 | ||||||
chr17:74799905
|
C | T | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.636+4273C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74799905 | ||||||
chr17:74800527
|
G | C | 40 | a0001c0001t0001g0190a0001c0001t0002g0204a0001c0001t0002g0228others(37): Show | 42 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+4895G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800527 | ||||||
chr17:74800528
|
C | T | 40 | a0001c0001t0001g0190a0001c0001t0002g0204a0001c0001t0002g0228others(37): Show | 42 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+4896C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800528 | ||||||
chr17:74800563
|
G | A | 78 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(75): Show | 80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.636+4931G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800563 | ||||||
chr17:74800781
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.636+5149G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800781 | ||||||
chr17:74800795
|
T | TG | 124 | a0001c0001t0001g0083a0001c0001t0001g0277a0001c0001t0001g0278others(121): Show | 126 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.636+5164dupG | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74800795 | |||||
chr17:74800914
|
T | C | 1 | a0001c0001t0004g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.636+5282T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74800914 | ||||||
chr17:74801086
|
C | T | 4 | a0001c0001t0008g0026a0001c0001t0008g0036a0002c0005t0007g0068others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+5454C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801086 | ||||||
chr17:74801227
|
G | A | 18 | a0001c0001t0004g0045a0001c0001t0004g0048a0001c0001t0004g0050others(15): Show | 18 | HG01099.hp2 HG02055.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.636+5595G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801227 | ||||||
chr17:74801254
|
T | C | 17 | a0001c0001t0001g0083a0001c0001t0001g0278a0001c0001t0001g0279others(14): Show | 17 | HG00438.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.636+5622T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801254 | ||||||
chr17:74801333
|
A | G | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+5701A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801333 | ||||||
chr17:74801385
|
CGAGGTGT others(82): Show |
C | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+5807_636+5895d others(91): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74801385 | |||||
chr17:74801521
|
T | C | 1 | a0001c0001t0002g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.636+5889T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801521 | ||||||
chr17:74801643
|
G | A | 1 | a0002c0002t0029g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.636+6011G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801643 | ||||||
chr17:74801764
|
A | G | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.636+6132A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801764 | ||||||
chr17:74801861
|
G | A | 4 | a0001c0001t0008g0026a0001c0001t0008g0036a0002c0005t0007g0068others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+6229G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801861 | ||||||
chr17:74801968
|
G | A | 1 | a0001c0001t0009g0285 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.636+6336G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801968 | ||||||
chr17:74801974
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.636+6342C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74801974 | ||||||
chr17:74802021
|
A | G | 107 | a0001c0001t0001g0277a0001c0001t0002g0028a0001c0001t0002g0034others(104): Show | 109 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.636+6389A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802021 | ||||||
chr17:74802082
|
G | A | 1 | a0002c0002t0003g0143 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.636+6450G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802082 | ||||||
chr17:74802095
|
C | T | 78 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(75): Show | 80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.636+6463C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802095 | ||||||
chr17:74802123
|
T | G | 1 | a0002c0002t0004g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.636+6491T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802123 | ||||||
chr17:74802231
|
A | G | 3 | a0001c0001t0009g0289a0001c0001t0009g0290a0004c0014t0009g0293 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.636+6599A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802231 | ||||||
chr17:74802259
|
G | A | 76 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(73): Show | 78 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.636+6627G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802259 | ||||||
chr17:74802293
|
A | G | 77 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.636+6661A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802293 | ||||||
chr17:74802304
|
G | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0018 | 3 | HG00642.hp2 HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.636+6672G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802304 | ||||||
chr17:74802341
|
A | G | 1 | a0001c0001t0008g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.636+6709A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802341 | ||||||
chr17:74802508
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.636+6876G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802508 | ||||||
chr17:74802539
|
G | C | 1 | a0001c0001t0002g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.636+6907G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802539 | ||||||
chr17:74802701
|
G | T | 1 | a0002c0003t0001g0105 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.636+7069G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802701 | ||||||
chr17:74802760
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+7128G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802760 | ||||||
chr17:74802886
|
C | T | 1 | a0003c0009t0002g0019 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.636+7254C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74802886 | ||||||
chr17:74803165
|
T | C | 1 | a0002c0005t0034g0067 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.636+7533T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803165 | ||||||
chr17:74803201
|
G | A | 99 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(96): Show | 101 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.636+7569G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803201 | ||||||
chr17:74803283
|
C | G | 1 | a0002c0002t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.636+7651C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803283 | ||||||
chr17:74803355
|
T | C | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.636+7723T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803355 | ||||||
chr17:74803474
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+7842G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803474 | ||||||
chr17:74803499
|
A | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+7867A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803499 | ||||||
chr17:74803606
|
C | A | 1 | a0001c0001t0005g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.636+7974C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803606 | ||||||
chr17:74803702
|
A | G | 1 | a0001c0001t0002g0219 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.636+8070A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803702 | ||||||
chr17:74803724
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.636+8092C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74803724 | ||||||
chr17:74804005
|
T | C | 68 | a0001c0001t0001g0277a0001c0001t0002g0245a0001c0001t0003g0081others(65): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.636+8373T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804005 | ||||||
chr17:74804011
|
A | G | 1 | a0001c0001t0002g0213 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.636+8379A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804011 | ||||||
chr17:74804149
|
T | C | 4 | a0001c0001t0008g0026a0001c0001t0008g0036a0002c0005t0007g0068others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+8517T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804149 | ||||||
chr17:74804191
|
A | G | 1 | a0002c0005t0007g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.636+8559A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804191 | ||||||
chr17:74804195
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.636+8563G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804195 | ||||||
chr17:74804213
|
T | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+8581T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804213 | ||||||
chr17:74804288
|
T | C | 274 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(271): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.636+8656T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804288 | ||||||
chr17:74804499
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+8867G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804499 | ||||||
chr17:74804615
|
G | C | 16 | a0001c0001t0001g0083a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00438.hp1 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.636+8983G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804615 | ||||||
chr17:74804739
|
C | T | 1 | a0002c0002t0001g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.636+9107C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804739 | ||||||
chr17:74804768
|
A | G | 78 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(75): Show | 80 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.636+9136A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804768 | ||||||
chr17:74804808
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.636+9176G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804808 | ||||||
chr17:74804916
|
T | C | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+9284T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804916 | ||||||
chr17:74804983
|
G | A | 74 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(71): Show | 76 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.636+9351G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74804983 | ||||||
chr17:74805172
|
C | T | 3 | a0002c0002t0003g0004a0002c0002t0003g0096a0002c0019t0003g0149 | 4 | HG00438.hp2 NA19002.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+9540C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805172 | ||||||
chr17:74805248
|
T | C | 102 | a0001c0001t0001g0277a0001c0001t0002g0028a0001c0001t0002g0034others(99): Show | 104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.636+9616T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805248 | ||||||
chr17:74805371
|
A | C | 3 | a0001c0001t0004g0045a0001c0001t0004g0048a0001c0001t0004g0050 | 3 | HG03486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.636+9739A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805371 | ||||||
chr17:74805375
|
G | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+9743G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805375 | ||||||
chr17:74805417
|
T | C | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+9785T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805417 | ||||||
chr17:74805470
|
G | A | 99 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(96): Show | 101 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.636+9838G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805470 | ||||||
chr17:74805567
|
G | C | 99 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(96): Show | 101 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.636+9935G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805567 | ||||||
chr17:74805647
|
C | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.636+10015C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805647 | ||||||
chr17:74805657
|
C | T | 2 | a0001c0001t0002g0248a0002c0002t0001g0121 | 2 | HG01192.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.636+10025C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805657 | ||||||
chr17:74805758
|
C | T | 1 | a0002c0002t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.636+10126C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805758 | ||||||
chr17:74805769
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+10137G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74805769 | ||||||
chr17:74806003
|
C | G | 3 | a0001c0001t0009g0289a0001c0001t0009g0290a0004c0014t0009g0293 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.636+10371C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806003 | ||||||
chr17:74806054
|
T | C | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+10422T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806054 | ||||||
chr17:74806297
|
C | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.636+10665C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806297 | ||||||
chr17:74806376
|
G | A | 1 | a0001c0004t0013g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.636+10744G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806376 | ||||||
chr17:74806425
|
G | C | 4 | a0001c0001t0008g0026a0001c0001t0008g0036a0002c0005t0007g0068others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+10793G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806425 | ||||||
chr17:74806497
|
C | T | 1 | a0002c0002t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.636+10865C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806497 | ||||||
chr17:74806590
|
A | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.636+10958A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806590 | ||||||
chr17:74806626
|
T | C | 101 | a0001c0001t0001g0277a0001c0001t0002g0028a0001c0001t0002g0034others(98): Show | 103 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.636+10994T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806626 | ||||||
chr17:74806640
|
C | T | 3 | a0001c0001t0008g0193a0001c0001t0015g0023a0001c0001t0015g0043 | 3 | HG01099.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.636+11008C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806640 | ||||||
chr17:74806751
|
C | T | 1 | a0001c0001t0006g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.636+11119C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806751 | ||||||
chr17:74806864
|
C | T | 3 | a0001c0001t0004g0052a0001c0001t0025g0222a0001c0010t0018g0288 | 3 | HG02630.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.636+11232C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806864 | ||||||
chr17:74806888
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0216 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.636+11256G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806888 | ||||||
chr17:74806930
|
C | T | 1 | a0001c0011t0006g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.636+11298C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74806930 | ||||||
chr17:74807069
|
G | T | 2 | a0002c0002t0001g0100a0002c0002t0001g0117 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.636+11437G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807069 | ||||||
chr17:74807086
|
C | G | 3 | a0001c0001t0002g0242a0001c0001t0005g0238a0002c0002t0001g0139 | 3 | HG01074.hp2 HG02451.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.636+11454C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807086 | ||||||
chr17:74807208
|
G | C | 167 | a0001c0001t0001g0083a0001c0001t0001g0190a0001c0001t0001g0277others(164): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.636+11576G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807208 | ||||||
chr17:74807386
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.636+11754G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807386 | ||||||
chr17:74807443
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.636+11811G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807443 | ||||||
chr17:74807606
|
C | G | 1 | a0002c0005t0001g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.636+11974C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807606 | ||||||
chr17:74807635
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.636+12003T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807635 | ||||||
chr17:74807755
|
C | A | 3 | a0001c0001t0004g0045a0001c0001t0004g0048a0001c0001t0004g0050 | 3 | HG03486.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.637-11995C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807755 | ||||||
chr17:74807755
|
C | T | 14 | a0001c0001t0002g0034a0001c0001t0002g0041a0001c0001t0003g0276others(11): Show | 14 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-11995C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807755 | ||||||
chr17:74807925
|
C | G | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-11825C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807925 | ||||||
chr17:74807937
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.637-11813G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807937 | ||||||
chr17:74807985
|
A | G | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-11765A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74807985 | ||||||
chr17:74808006
|
G | A | 1 | a0001c0021t0037g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.637-11744G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808006 | ||||||
chr17:74808122
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-11628G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808122 | ||||||
chr17:74808506
|
T | G | 7 | a0001c0004t0011g0286a0001c0004t0011g0287a0001c0004t0012g0047others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-11244T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808506 | ||||||
chr17:74808545
|
G | A | 2 | a0001c0001t0008g0193a0002c0002t0001g0140 | 2 | NA18959.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.637-11205G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808545 | ||||||
chr17:74808665
|
T | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-11085T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808665 | ||||||
chr17:74808670
|
T | C | 1 | a0004c0014t0009g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637-11080T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808670 | ||||||
chr17:74808688
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.637-11062C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808688 | ||||||
chr17:74808785
|
T | C | 6 | a0001c0001t0007g0049a0001c0004t0011g0286a0001c0004t0011g0287others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-10965T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808785 | ||||||
chr17:74808935
|
G | T | 1 | a0002c0002t0016g0097 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637-10815G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74808935 | ||||||
chr17:74809125
|
A | G | 1 | a0001c0004t0011g0286 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.637-10625A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809125 | ||||||
chr17:74809128
|
T | A | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637-10622T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809128 | ||||||
chr17:74809144
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637-10606G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809144 | ||||||
chr17:74809310
|
T | C | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-10440T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809310 | ||||||
chr17:74809588
|
G | A | 4 | a0002c0002t0004g0053a0002c0002t0004g0054a0002c0002t0004g0055others(1): Show | 4 | NA18955.hp1 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-10162G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809588 | ||||||
chr17:74809627
|
C | T | 97 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.637-10123C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809627 | ||||||
chr17:74809644
|
C | T | 159 | a0001c0001t0001g0083a0001c0001t0001g0277a0001c0001t0001g0278others(156): Show | 163 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.637-10106C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809644 | ||||||
chr17:74809841
|
C | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-9909C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809841 | ||||||
chr17:74809966
|
G | A | 2 | a0001c0001t0008g0026a0002c0005t0007g0068 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-9784G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809966 | ||||||
chr17:74809967
|
A | G | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-9783A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74809967 | ||||||
chr17:74810083
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-9667C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810083 | ||||||
chr17:74810306
|
C | T | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-9444C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810306 | ||||||
chr17:74810433
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.637-9317A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810433 | ||||||
chr17:74810619
|
A | T | 1 | a0002c0002t0030g0123 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.637-9131A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810619 | ||||||
chr17:74810701
|
C | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.637-9049C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810701 | ||||||
chr17:74810719
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0216 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.637-9031G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810719 | ||||||
chr17:74810775
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.637-8975G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810775 | ||||||
chr17:74810785
|
G | A | 1 | a0002c0002t0001g0142 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.637-8965G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810785 | ||||||
chr17:74810880
|
C | T | 4 | a0001c0001t0004g0048a0001c0001t0015g0023a0001c0001t0015g0043others(1): Show | 4 | HG01099.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-8870C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810880 | ||||||
chr17:74810882
|
G | A | 104 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(101): Show | 106 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.637-8868G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810882 | ||||||
chr17:74810898
|
G | A | 13 | a0001c0001t0001g0083a0001c0001t0001g0278a0001c0001t0001g0279others(10): Show | 13 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.637-8852G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810898 | ||||||
chr17:74810901
|
T | C | 1 | a0001c0001t0009g0285 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.637-8849T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74810901 | ||||||
chr17:74811037
|
A | C | 40 | a0001c0001t0002g0018a0001c0001t0002g0228a0001c0001t0004g0046others(37): Show | 42 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.637-8713A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811037 | ||||||
chr17:74811045
|
T | C | 82 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.637-8705T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811045 | ||||||
chr17:74811087
|
T | C | 2 | a0001c0001t0002g0214a0001c0001t0002g0216 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.637-8663T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811087 | ||||||
chr17:74811155
|
C | A | 1 | a0002c0005t0007g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.637-8595C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811155 | ||||||
chr17:74811425
|
C | T | 105 | a0001c0001t0001g0277a0001c0001t0002g0028a0001c0001t0002g0034others(102): Show | 107 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.637-8325C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811425 | ||||||
chr17:74811463
|
G | C | 82 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0041others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.637-8287G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811463 | ||||||
chr17:74811749
|
G | T | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.637-8001G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811749 | ||||||
chr17:74811770
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-7980G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811770 | ||||||
chr17:74811875
|
A | T | 1 | a0001c0001t0003g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.637-7875A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811875 | ||||||
chr17:74811878
|
T | A | 2 | a0002c0002t0003g0115a0002c0002t0003g0154 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.637-7872T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811878 | ||||||
chr17:74811891
|
A | C | 1 | a0001c0001t0006g0236 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.637-7859A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811891 | ||||||
chr17:74811928
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-7822C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811928 | ||||||
chr17:74811978
|
C | G | 17 | a0001c0001t0004g0045a0001c0001t0004g0048a0001c0001t0004g0050others(14): Show | 17 | HG01099.hp2 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.637-7772C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74811978 | ||||||
chr17:74812051
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637-7699G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812051 | ||||||
chr17:74812242
|
G | A | 14 | a0001c0001t0008g0026a0001c0001t0008g0036a0001c0004t0011g0286others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-7508G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812242 | ||||||
chr17:74812248
|
G | A | 12 | a0001c0001t0002g0228a0001c0001t0005g0194a0001c0004t0011g0286others(9): Show | 12 | HG00741.hp1 HG01516.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-7502G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812248 | ||||||
chr17:74812508
|
C | T | 68 | a0001c0001t0001g0277a0001c0001t0002g0273a0001c0001t0003g0188others(65): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.637-7242C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812508 | ||||||
chr17:74812631
|
G | A | 14 | a0001c0001t0008g0026a0001c0001t0008g0036a0001c0004t0011g0286others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-7119G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812631 | ||||||
chr17:74812637
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.637-7113G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812637 | ||||||
chr17:74812638
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-7112C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812638 | ||||||
chr17:74812735
|
G | A | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-7015G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812735 | ||||||
chr17:74812750
|
A | G | 2 | a0002c0002t0003g0115a0002c0002t0003g0154 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.637-7000A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74812750 | ||||||
chr17:74813115
|
G | A | 5 | a0001c0001t0004g0052a0001c0001t0005g0033a0001c0001t0005g0038others(2): Show | 5 | HG02486.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-6635G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813115 | ||||||
chr17:74813166
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-6584G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813166 | ||||||
chr17:74813224
|
A | G | 1 | a0002c0002t0001g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.637-6526A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813224 | ||||||
chr17:74813284
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637-6466C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813284 | ||||||
chr17:74813340
|
G | T | 2 | a0001c0001t0005g0238a0002c0002t0004g0183 | 2 | HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.637-6410G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813340 | ||||||
chr17:74813345
|
A | C | 1 | a0002c0002t0001g0099 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.637-6405A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813345 | ||||||
chr17:74813596
|
G | T | 2 | a0001c0001t0002g0030a0002c0002t0001g0180 | 2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.637-6154G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813596 | ||||||
chr17:74813931
|
G | A | 61 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0189others(58): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.637-5819G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813931 | ||||||
chr17:74813964
|
G | A | 1 | a0002c0002t0003g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.637-5786G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74813964 | ||||||
chr17:74814103
|
T | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0240a0001c0001t0002g0242others(1): Show | 4 | HG01074.hp2 HG02451.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-5647T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814103 | ||||||
chr17:74814228
|
C | T | 1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637-5522C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814228 | ||||||
chr17:74814242
|
TCCCAGGC others(43): Show |
T | 2 | a0002c0002t0001g0112a0002c0002t0001g0130 | 2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.637-5472_637-5423d others(52): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74814242 | |||||
chr17:74814242
|
TCCCAGGC others(102): Show |
T | 3 | a0002c0002t0003g0004a0002c0002t0003g0096a0002c0019t0003g0149 | 4 | HG00438.hp2 NA19002.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-5469_637-5361d others(2): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74814242 | |||||
chr17:74814553
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-5197G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814553 | ||||||
chr17:74814615
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.637-5135C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814615 | ||||||
chr17:74814658
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637-5092G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814658 | ||||||
chr17:74814685
|
T | G | 14 | a0001c0001t0004g0052a0001c0001t0005g0029a0001c0001t0005g0033others(11): Show | 16 | HG00639.hp2 HG01074.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-5065T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814685 | ||||||
chr17:74814939
|
C | G | 2 | a0002c0005t0001g0066a0002c0005t0001g0076 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.637-4811C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74814939 | ||||||
chr17:74815193
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4557G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815193 | ||||||
chr17:74815195
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4555G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815195 | ||||||
chr17:74815204
|
A | G | 73 | a0001c0001t0001g0277a0001c0001t0003g0081a0001c0001t0003g0188others(70): Show | 75 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.637-4546A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815204 | ||||||
chr17:74815332
|
A | G | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4418A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815332 | ||||||
chr17:74815336
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-4414G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815336 | ||||||
chr17:74815378
|
G | A | 10 | a0001c0001t0006g0253a0001c0001t0006g0255a0002c0002t0003g0005others(7): Show | 11 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-4372G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815378 | ||||||
chr17:74815444
|
T | C | 3 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280 | 3 | HG02055.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.637-4306T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815444 | ||||||
chr17:74815547
|
C | T | 1 | a0002c0002t0017g0093 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.637-4203C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815547 | ||||||
chr17:74815557
|
G | A | 1 | a0001c0004t0011g0291 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637-4193G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815557 | ||||||
chr17:74815563
|
C | T | 1 | a0002c0002t0001g0140 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.637-4187C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815563 | ||||||
chr17:74815574
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.637-4176C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815574 | ||||||
chr17:74815920
|
G | A | 1 | a0001c0001t0009g0284 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.637-3830G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815920 | ||||||
chr17:74815936
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3814C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815936 | ||||||
chr17:74815962
|
C | T | 1 | a0002c0002t0001g0168 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.637-3788C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815962 | ||||||
chr17:74815991
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.637-3759G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74815991 | ||||||
chr17:74816186
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3564C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816186 | ||||||
chr17:74816234
|
A | G | 1 | a0001c0001t0009g0284 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.637-3516A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816234 | ||||||
chr17:74816386
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3364C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816386 | ||||||
chr17:74816391
|
G | T | 1 | a0002c0002t0001g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.637-3359G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816391 | ||||||
chr17:74816401
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3349C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816401 | ||||||
chr17:74816629
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-3121C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816629 | ||||||
chr17:74816677
|
G | GT | 9 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0041others(6): Show | 9 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-3064dupT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 74816677 | |||||
chr17:74816711
|
C | T | 11 | a0001c0006t0002g0202a0001c0006t0002g0205a0001c0006t0002g0212others(8): Show | 12 | HG01346.hp1 HG01433.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-3039C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816711 | ||||||
chr17:74816714
|
C | T | 2 | a0002c0002t0003g0169a0002c0002t0003g0181 | 2 | NA18953.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.637-3036C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816714 | ||||||
chr17:74816840
|
T | C | 38 | a0001c0001t0001g0277a0001c0001t0003g0081a0001c0001t0003g0188others(35): Show | 39 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.637-2910T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816840 | ||||||
chr17:74816850
|
G | T | 1 | a0002c0002t0001g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.637-2900G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74816850 | ||||||
chr17:74817021
|
G | C | 291 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(288): Show | 300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.637-2729G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817021 | ||||||
chr17:74817063
|
C | T | 1 | a0001c0001t0002g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-2687C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817063 | ||||||
chr17:74817101
|
G | A | 3 | a0001c0001t0008g0229a0001c0021t0037g0009a0002c0002t0001g0058 | 3 | HG00733.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.637-2649G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817101 | ||||||
chr17:74817202
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-2548G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817202 | ||||||
chr17:74817301
|
C | T | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.637-2449C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817301 | ||||||
chr17:74817420
|
G | C | 15 | a0001c0001t0008g0026a0001c0001t0008g0036a0001c0004t0011g0286others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-2330G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817420 | ||||||
chr17:74817688
|
G | C | 64 | a0001c0001t0001g0277a0001c0001t0003g0081a0001c0001t0003g0188others(61): Show | 66 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.637-2062G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817688 | ||||||
chr17:74817874
|
C | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-1876C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817874 | ||||||
chr17:74817945
|
C | A | 1 | a0002c0002t0036g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.637-1805C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817945 | ||||||
chr17:74817996
|
G | A | 11 | a0001c0004t0011g0286a0001c0004t0011g0287a0001c0004t0011g0291others(8): Show | 11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-1754G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74817996 | ||||||
chr17:74818033
|
A | G | 1 | a0001c0001t0002g0251 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.637-1717A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818033 | ||||||
chr17:74818192
|
C | T | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-1558C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818192 | ||||||
chr17:74818248
|
A | G | 104 | a0001c0001t0001g0277a0001c0001t0002g0242a0001c0001t0003g0081others(101): Show | 106 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.637-1502A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818248 | ||||||
chr17:74818340
|
G | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-1410G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818340 | ||||||
chr17:74818427
|
A | T | 2 | a0001c0001t0017g0082a0002c0002t0017g0093 | 2 | HG00673.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.637-1323A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818427 | ||||||
chr17:74818437
|
A | G | 165 | a0001c0001t0001g0083a0001c0001t0001g0277a0001c0001t0001g0278others(162): Show | 169 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.637-1313A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818437 | ||||||
chr17:74818452
|
A | G | 16 | a0001c0001t0001g0277a0001c0001t0006g0221a0001c0001t0006g0236others(13): Show | 17 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.637-1298A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818452 | ||||||
chr17:74818483
|
C | T | 3 | a0001c0001t0006g0203a0003c0009t0006g0011a0007c0016t0006g0016 | 3 | NA18947.hp2 NA18983.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.637-1267C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818483 | ||||||
chr17:74818533
|
G | A | 1 | a0001c0001t0021g0247 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.637-1217G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818533 | ||||||
chr17:74818658
|
C | T | 1 | a0002c0002t0004g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637-1092C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74818658 | ||||||
chr17:74819010
|
C | G | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.637-740C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819010 | ||||||
chr17:74819055
|
G | A | 15 | a0001c0001t0002g0198a0001c0001t0002g0235a0001c0001t0002g0240others(12): Show | 15 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-695G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819055 | ||||||
chr17:74819333
|
A | T | 2 | a0001c0004t0012g0047a0002c0007t0012g0069 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.637-417A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819333 | ||||||
chr17:74819464
|
G | C | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.637-286G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819464 | ||||||
chr17:74819517
|
C | T | 1 | a0003c0009t0002g0019 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.637-233C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819517 | ||||||
chr17:74819662
|
G | A | 2 | a0001c0001t0005g0230a0001c0001t0005g0233 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.637-88G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819662 | ||||||
chr17:74819690
|
G | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.637-60G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 8/9 | chr17 | 74819690 | ||||||
chr17:74819874
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0278a0001c0001t0001g0279others(8): Show | 11 | HG01069.hp1 HG01192.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+31G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74819874 | ||||||
chr17:74819996
|
A | C | 2 | a0001c0001t0015g0023a0001c0001t0015g0043 | 2 | HG01099.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.730+153A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74819996 | ||||||
chr17:74820074
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+231G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820074 | ||||||
chr17:74820153
|
A | G | 6 | a0001c0001t0008g0015a0001c0001t0008g0193a0001c0001t0028g0021others(3): Show | 6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+310A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820153 | ||||||
chr17:74820241
|
G | A | 1 | a0001c0001t0004g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.730+398G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820241 | ||||||
chr17:74820402
|
C | T | 1 | a0001c0004t0013g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730+559C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820402 | ||||||
chr17:74820628
|
C | T | 73 | a0001c0001t0001g0277a0001c0001t0003g0081a0001c0001t0003g0188others(70): Show | 75 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.730+785C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820628 | ||||||
chr17:74820810
|
G | A | 22 | a0001c0001t0004g0048a0001c0001t0008g0026a0001c0001t0008g0036others(19): Show | 22 | HG00733.hp2 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.730+967G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820810 | ||||||
chr17:74820915
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.730+1072C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820915 | ||||||
chr17:74820928
|
T | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+1085T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74820928 | ||||||
chr17:74821021
|
G | A | 3 | a0001c0001t0008g0229a0001c0021t0037g0009a0002c0002t0001g0058 | 3 | HG00733.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.730+1178G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821021 | ||||||
chr17:74821121
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0002g0034 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.730+1278G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821121 | ||||||
chr17:74821246
|
C | G | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+1403C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821246 | ||||||
chr17:74821711
|
A | G | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+1868A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821711 | ||||||
chr17:74821875
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+2032G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821875 | ||||||
chr17:74821986
|
T | C | 16 | a0001c0001t0005g0226a0001c0001t0008g0026a0001c0001t0008g0036others(13): Show | 16 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.730+2143T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74821986 | ||||||
chr17:74822101
|
G | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0051 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.730+2258G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822101 | ||||||
chr17:74822143
|
C | T | 6 | a0001c0001t0008g0015a0001c0001t0008g0193a0001c0001t0028g0021others(3): Show | 6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+2300C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822143 | ||||||
chr17:74822213
|
G | T | 1 | a0001c0001t0002g0259 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.730+2370G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822213 | ||||||
chr17:74822341
|
C | A | 1 | a0002c0002t0003g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.730+2498C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822341 | ||||||
chr17:74822360
|
C | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0223 | 2 | HG00738.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.730+2517C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822360 | ||||||
chr17:74822641
|
A | G | 3 | a0001c0001t0008g0229a0001c0021t0037g0009a0002c0002t0001g0058 | 3 | HG00733.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.730+2798A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822641 | ||||||
chr17:74822738
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.730+2895G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822738 | ||||||
chr17:74822865
|
C | T | 49 | a0001c0001t0001g0044a0001c0001t0001g0184a0001c0001t0001g0190others(46): Show | 51 | HG00408.hp2 HG00544.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.730+3022C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822865 | ||||||
chr17:74822881
|
C | A | 1 | a0001c0001t0002g0215 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.730+3038C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822881 | ||||||
chr17:74822894
|
C | T | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+3051C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822894 | ||||||
chr17:74822925
|
G | C | 9 | a0001c0001t0002g0235a0001c0001t0002g0240a0001c0001t0002g0242others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+3082G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822925 | ||||||
chr17:74822940
|
G | A | 13 | a0001c0001t0001g0083a0001c0001t0001g0278a0001c0001t0001g0279others(10): Show | 13 | HG00423.hp2 HG01069.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.730+3097G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822940 | ||||||
chr17:74822994
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.730+3151C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74822994 | ||||||
chr17:74823043
|
A | G | 36 | a0001c0001t0001g0184a0001c0001t0002g0035a0001c0001t0002g0039others(33): Show | 37 | HG00408.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.730+3200A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823043 | ||||||
chr17:74823119
|
C | A | 1 | a0001c0001t0002g0270 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.730+3276C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823119 | ||||||
chr17:74823136
|
G | A | 1 | a0002c0002t0001g0150 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.730+3293G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823136 | ||||||
chr17:74823205
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.730+3362C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823205 | ||||||
chr17:74823424
|
C | G | 5 | a0001c0001t0008g0015a0001c0001t0028g0021a0001c0008t0007g0162others(2): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+3581C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823424 | ||||||
chr17:74823957
|
A | G | 283 | a0001c0001t0001g0044a0001c0001t0001g0083a0001c0001t0001g0184others(280): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.730+4114A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823957 | ||||||
chr17:74823962
|
G | A | 1 | a0002c0002t0016g0097 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.730+4119G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74823962 | ||||||
chr17:74824125
|
T | C | 16 | a0001c0001t0005g0029a0001c0001t0015g0023a0001c0001t0015g0043others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+4282T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824125 | ||||||
chr17:74824199
|
G | A | 1 | a0002c0002t0004g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.730+4356G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824199 | ||||||
chr17:74824215
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.730+4372T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824215 | ||||||
chr17:74824230
|
C | A | 1 | a0002c0002t0001g0136 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.730+4387C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824230 | ||||||
chr17:74824295
|
C | T | 3 | a0001c0001t0015g0023a0001c0001t0015g0043a0001c0001t0019g0283 | 3 | HG01099.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.730+4452C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824295 | ||||||
chr17:74824368
|
A | G | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.730+4525A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824368 | ||||||
chr17:74824426
|
C | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+4583C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824426 | ||||||
chr17:74824453
|
T | C | 39 | a0001c0001t0003g0276a0001c0001t0007g0049a0001c0001t0008g0015others(36): Show | 39 | HG00639.hp1 HG00733.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.730+4610T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824453 | ||||||
chr17:74824454
|
G | C | 14 | a0001c0001t0003g0276a0001c0001t0008g0015a0001c0001t0008g0193others(11): Show | 14 | HG00639.hp1 HG02015.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.730+4611G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824454 | ||||||
chr17:74824455
|
C | A | 5 | a0001c0001t0003g0276a0002c0002t0003g0057a0002c0002t0003g0115others(2): Show | 5 | HG02015.hp2 HG02132.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+4612C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824455 | ||||||
chr17:74824462
|
G | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0138 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.730+4619G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824462 | ||||||
chr17:74824527
|
G | A | 2 | a0002c0002t0003g0115a0002c0002t0003g0154 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.730+4684G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824527 | ||||||
chr17:74824562
|
G | A | 60 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0189others(57): Show | 63 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.730+4719G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824562 | ||||||
chr17:74824601
|
G | A | 15 | a0001c0001t0008g0026a0001c0001t0008g0036a0001c0004t0011g0286others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.730+4758G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824601 | ||||||
chr17:74824660
|
C | T | 3 | a0001c0001t0004g0046a0001c0001t0005g0025a0002c0002t0004g0065 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.730+4817C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824660 | ||||||
chr17:74824865
|
G | A | 1 | a0002c0002t0004g0054 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.730+5022G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74824865 | ||||||
chr17:74825257
|
A | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0002g0250others(3): Show | 6 | HG00408.hp1 NA18612.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+5414A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825257 | ||||||
chr17:74825285
|
G | C | 1 | a0002c0002t0001g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.730+5442G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825285 | ||||||
chr17:74825540
|
T | A | 20 | a0001c0001t0008g0026a0001c0001t0008g0036a0001c0001t0008g0225others(17): Show | 20 | HG00438.hp1 HG01099.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.730+5697T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825540 | ||||||
chr17:74825607
|
G | A | 5 | a0001c0001t0006g0244a0001c0001t0006g0266a0001c0001t0006g0274others(2): Show | 5 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+5764G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825607 | ||||||
chr17:74825634
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.730+5791G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825634 | ||||||
chr17:74825765
|
C | G | 3 | a0001c0001t0010g0294a0001c0001t0010g0295a0002c0005t0004g0164 | 3 | HG02615.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.730+5922C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825765 | ||||||
chr17:74825769
|
C | A | 10 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(7): Show | 10 | HG01069.hp1 HG01192.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.730+5926C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825769 | ||||||
chr17:74825817
|
G | C | 71 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.730+5974G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825817 | ||||||
chr17:74825874
|
C | T | 6 | a0001c0001t0002g0024a0001c0001t0002g0028a0001c0001t0002g0051others(3): Show | 6 | HG00738.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+6031C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825874 | ||||||
chr17:74825977
|
G | A | 1 | a0001c0001t0005g0238 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.730+6134G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74825977 | ||||||
chr17:74826150
|
A | G | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.730+6307A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826150 | ||||||
chr17:74826239
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.730+6396G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826239 | ||||||
chr17:74826300
|
GCTGCCAC others(3): Show |
G | 2 | a0001c0001t0015g0023a0001c0001t0015g0043 | 2 | HG01099.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.730+6466_730+6475d others(12): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74826300 | |||||
chr17:74826328
|
G | A | 1 | a0001c0001t0005g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.730+6485G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826328 | ||||||
chr17:74826364
|
T | C | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+6521T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826364 | ||||||
chr17:74826399
|
C | G | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+6556C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826399 | ||||||
chr17:74826421
|
C | T | 3 | a0001c0001t0009g0289a0001c0001t0009g0290a0004c0014t0009g0293 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.730+6578C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826421 | ||||||
chr17:74826507
|
C | G | 1 | a0001c0001t0008g0225 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.730+6664C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826507 | ||||||
chr17:74826556
|
A | C | 71 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.730+6713A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826556 | ||||||
chr17:74826577
|
C | G | 1 | a0001c0001t0008g0225 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.730+6734C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826577 | ||||||
chr17:74826589
|
G | A | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+6746G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826589 | ||||||
chr17:74826817
|
G | A | 63 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(60): Show | 65 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.730+6974G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826817 | ||||||
chr17:74826880
|
G | A | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.730+7037G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74826880 | ||||||
chr17:74827066
|
T | C | 71 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.730+7223T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827066 | ||||||
chr17:74827174
|
G | A | 1 | a0001c0001t0005g0029 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.730+7331G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827174 | ||||||
chr17:74827175
|
C | A | 1 | a0001c0001t0006g0253 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.730+7332C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827175 | ||||||
chr17:74827220
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.730+7377G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827220 | ||||||
chr17:74827298
|
CT | C | 6 | a0001c0001t0002g0270a0001c0001t0004g0052a0001c0001t0006g0244others(3): Show | 6 | HG03195.hp2 HG03491.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+7471delT | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74827298 | |||||
chr17:74827510
|
G | A | 3 | a0001c0001t0015g0023a0001c0001t0015g0043a0001c0001t0019g0283 | 3 | HG01099.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.730+7667G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827510 | ||||||
chr17:74827597
|
C | T | 4 | a0001c0006t0002g0202a0001c0006t0002g0205a0001c0006t0002g0212others(1): Show | 4 | NA18971.hp1 NA18983.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+7754C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827597 | ||||||
chr17:74827890
|
A | G | 1 | a0002c0002t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.731-8037A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827890 | ||||||
chr17:74827911
|
A | AT | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-8016_731-8015i others(3): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827911 | ||||||
chr17:74827926
|
C | T | 3 | a0001c0001t0009g0289a0001c0001t0009g0290a0004c0014t0009g0293 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.731-8001C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827926 | ||||||
chr17:74827983
|
C | T | 1 | a0001c0001t0008g0229 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.731-7944C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74827983 | ||||||
chr17:74828137
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.731-7790C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828137 | ||||||
chr17:74828304
|
G | T | 1 | a0002c0002t0003g0108 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.731-7623G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828304 | ||||||
chr17:74828361
|
T | A | 1 | a0001c0001t0027g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.731-7566T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828361 | ||||||
chr17:74828477
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.731-7450C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828477 | ||||||
chr17:74828744
|
GAGA | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0027a0001c0001t0002g0041others(2): Show | 6 | HG01243.hp2 HG02818.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-7180_731-7178d others(5): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74828744 | |||||
chr17:74828809
|
A | C | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.731-7118A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828809 | ||||||
chr17:74828904
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.731-7023C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828904 | ||||||
chr17:74828958
|
C | T | 15 | a0001c0001t0008g0026a0001c0001t0008g0036a0001c0004t0011g0286others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.731-6969C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74828958 | ||||||
chr17:74829096
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.731-6831G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829096 | ||||||
chr17:74829155
|
G | A | 2 | a0001c0001t0025g0222a0001c0010t0018g0288 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.731-6772G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829155 | ||||||
chr17:74829269
|
G | A | 11 | a0001c0004t0011g0286a0001c0004t0011g0287a0001c0004t0011g0291others(8): Show | 11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-6658G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829269 | ||||||
chr17:74829334
|
G | A | 39 | a0001c0001t0004g0046a0001c0001t0004g0052a0001c0001t0005g0014others(36): Show | 41 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.731-6593G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829334 | ||||||
chr17:74829395
|
A | G | 5 | a0001c0001t0002g0017a0001c0001t0002g0037a0001c0001t0002g0259others(2): Show | 5 | HG00733.hp1 HG01106.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-6532A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829395 | ||||||
chr17:74829538
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0031a0001c0001t0014g0210 | 3 | NA18948.hp1 NA18984.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.731-6389C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829538 | ||||||
chr17:74829540
|
A | G | 1 | a0002c0002t0001g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.731-6387A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829540 | ||||||
chr17:74829672
|
A | C | 1 | a0005c0015t0008g0275 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.731-6255A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829672 | ||||||
chr17:74829721
|
G | T | 21 | a0001c0001t0008g0026a0001c0001t0008g0036a0001c0001t0008g0225others(18): Show | 21 | HG00733.hp2 HG01099.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.731-6206G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829721 | ||||||
chr17:74829742
|
C | T | 2 | a0001c0001t0005g0220a0002c0002t0001g0090 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.731-6185C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829742 | ||||||
chr17:74829762
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.731-6165C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829762 | ||||||
chr17:74829767
|
A | C | 1 | a0001c0001t0002g0270 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.731-6160A>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829767 | ||||||
chr17:74829810
|
C | T | 1 | a0002c0003t0001g0101 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.731-6117C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829810 | ||||||
chr17:74829820
|
T | G | 1 | a0001c0001t0005g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.731-6107T>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829820 | ||||||
chr17:74829993
|
G | A | 1 | a0001c0001t0028g0021 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.731-5934G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74829993 | ||||||
chr17:74830104
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.731-5823G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830104 | ||||||
chr17:74830150
|
A | G | 1 | a0001c0001t0005g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.731-5777A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830150 | ||||||
chr17:74830605
|
A | G | 1 | a0002c0002t0003g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.731-5322A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830605 | ||||||
chr17:74830636
|
C | T | 2 | a0001c0001t0002g0258a0001c0001t0021g0247 | 2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.731-5291C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830636 | ||||||
chr17:74830713
|
G | T | 1 | a0001c0001t0002g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.731-5214G>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830713 | ||||||
chr17:74830939
|
G | A | 71 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-4988G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74830939 | ||||||
chr17:74831132
|
A | ACC | 11 | a0001c0004t0011g0286a0001c0004t0011g0287a0001c0004t0011g0291others(8): Show | 11 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-4794_731-4793d others(4): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74831132 | |||||
chr17:74831134
|
C | G | 1 | a0001c0001t0002g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.731-4793C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831134 | ||||||
chr17:74831184
|
T | A | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-4743T>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831184 | ||||||
chr17:74831185
|
C | T | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-4742C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831185 | ||||||
chr17:74831222
|
G | A | 2 | a0002c0002t0001g0100a0002c0002t0001g0117 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.731-4705G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831222 | ||||||
chr17:74831304
|
C | A | 71 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-4623C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831304 | ||||||
chr17:74831407
|
C | T | 2 | a0001c0001t0002g0030a0002c0002t0001g0180 | 2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.731-4520C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831407 | ||||||
chr17:74831408
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.731-4519A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831408 | ||||||
chr17:74831525
|
C | T | 1 | a0002c0002t0003g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.731-4402C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831525 | ||||||
chr17:74831546
|
C | G | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-4381C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831546 | ||||||
chr17:74831742
|
G | A | 2 | a0001c0001t0002g0258a0001c0001t0021g0247 | 2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.731-4185G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74831742 | ||||||
chr17:74832012
|
T | C | 13 | a0001c0001t0008g0229a0001c0004t0011g0286a0001c0004t0011g0287others(10): Show | 13 | HG00733.hp2 HG01106.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.731-3915T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832012 | ||||||
chr17:74832074
|
C | CA | 71 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-3851dupA | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74832074 | |||||
chr17:74832133
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.731-3794A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832133 | ||||||
chr17:74832246
|
C | T | 1 | a0001c0001t0002g0267 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.731-3681C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832246 | ||||||
chr17:74832532
|
A | G | 1 | a0002c0002t0001g0150 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.731-3395A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832532 | ||||||
chr17:74832611
|
G | A | 1 | a0009c0018t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.731-3316G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832611 | ||||||
chr17:74832664
|
G | A | 1 | a0002c0002t0004g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.731-3263G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832664 | ||||||
chr17:74832761
|
C | T | 1 | a0002c0002t0004g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.731-3166C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832761 | ||||||
chr17:74832834
|
G | A | 4 | a0001c0001t0002g0282a0002c0002t0001g0084a0002c0002t0001g0091others(1): Show | 4 | NA18968.hp1 NA19056.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-3093G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832834 | ||||||
chr17:74832950
|
A | G | 2 | a0001c0001t0007g0049a0002c0002t0007g0059 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.731-2977A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832950 | ||||||
chr17:74832993
|
T | C | 4 | a0001c0001t0015g0023a0001c0001t0015g0043a0001c0001t0019g0283others(1): Show | 4 | HG00438.hp1 HG01099.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-2934T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832993 | ||||||
chr17:74832998
|
T | C | 1 | a0001c0001t0008g0225 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.731-2929T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74832998 | ||||||
chr17:74833015
|
G | GACTT | 87 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(84): Show | 89 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.731-2912_731-2911i others(6): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833015 | ||||||
chr17:74833015
|
G | GACTTGTT others(1): Show |
6 | a0001c0001t0015g0023a0001c0001t0015g0043a0001c0001t0019g0283others(3): Show | 6 | HG00438.hp1 HG01099.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-2912_731-2911i others(10): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833015 | ||||||
chr17:74833017
|
C | CTTGT | 3 | a0001c0001t0007g0049a0002c0002t0001g0178a0002c0002t0007g0059 | 3 | HG01884.hp2 HG02145.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.731-2891_731-2888d others(6): Show |
TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 74833017 | |||||
chr17:74833017
|
C | T | 93 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(90): Show | 95 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.731-2910C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833017 | ||||||
chr17:74833086
|
C | T | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.731-2841C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833086 | ||||||
chr17:74833323
|
T | C | 1 | a0002c0002t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.731-2604T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833323 | ||||||
chr17:74833595
|
G | A | 4 | a0001c0001t0015g0023a0001c0001t0015g0043a0001c0001t0019g0283others(1): Show | 4 | HG00438.hp1 HG01099.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-2332G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833595 | ||||||
chr17:74833612
|
G | C | 1 | a0001c0004t0011g0292 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.731-2315G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833612 | ||||||
chr17:74833627
|
A | T | 3 | a0001c0001t0009g0289a0001c0001t0009g0290a0004c0014t0009g0293 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.731-2300A>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833627 | ||||||
chr17:74833668
|
T | C | 1 | a0002c0019t0003g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.731-2259T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833668 | ||||||
chr17:74833703
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.731-2224C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833703 | ||||||
chr17:74833746
|
A | G | 93 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(90): Show | 95 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.731-2181A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833746 | ||||||
chr17:74833864
|
C | G | 1 | a0001c0001t0008g0229 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.731-2063C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833864 | ||||||
chr17:74833882
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.731-2045G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833882 | ||||||
chr17:74833967
|
C | T | 4 | a0001c0001t0005g0033a0001c0001t0005g0038a0001c0001t0005g0230others(1): Show | 4 | HG02486.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1960C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833967 | ||||||
chr17:74833989
|
C | A | 1 | a0002c0002t0004g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.731-1938C>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74833989 | ||||||
chr17:74834107
|
G | C | 1 | a0001c0001t0002g0242 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.731-1820G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834107 | ||||||
chr17:74834259
|
T | C | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-1668T>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834259 | ||||||
chr17:74834293
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G | A | 66 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.731-1634G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834293 | ||||||
chr17:74834412
|
C | T | 1 | a0002c0005t0004g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.731-1515C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834412 | ||||||
chr17:74834719
|
G | C | 3 | a0001c0001t0006g0255a0002c0002t0003g0005a0002c0002t0031g0128 | 4 | HG00642.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1208G>C | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834719 | ||||||
chr17:74834732
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G | A | 97 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(94): Show | 99 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.731-1195G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834732 | ||||||
chr17:74834833
|
C | T | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.731-1094C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834833 | ||||||
chr17:74834899
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C | T | 2 | a0001c0004t0012g0047a0002c0007t0012g0069 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.731-1028C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834899 | ||||||
chr17:74834985
|
C | T | 2 | a0001c0001t0004g0052a0001c0001t0005g0029 | 2 | HG00639.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.731-942C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74834985 | ||||||
chr17:74835019
|
C | T | 1 | a0002c0002t0003g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.731-908C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835019 | ||||||
chr17:74835304
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C | G | 1 | a0001c0001t0008g0225 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.731-623C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835304 | ||||||
chr17:74835761
|
G | A | 1 | a0002c0002t0004g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.731-166G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835761 | ||||||
chr17:74835801
|
A | G | 1 | a0001c0001t0022g0252 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.731-126A>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835801 | ||||||
chr17:74835845
|
C | T | 1 | a0002c0002t0035g0075 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.731-82C>T | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835845 | ||||||
chr17:74835854
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G | A | 4 | a0001c0001t0002g0235a0001c0001t0002g0240a0001c0001t0002g0242others(1): Show | 4 | HG01074.hp2 HG02451.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-73G>A | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835854 | ||||||
chr17:74835893
|
C | G | 74 | a0001c0001t0003g0081a0001c0001t0003g0188a0001c0001t0003g0276others(71): Show | 76 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.731-34C>G | TMEM104 | ENSG00000109066.14 | transcript | ENST00000335464.10 | protein_coding | 9/9 | chr17 | 74835893 |