geneid | 91147 |
---|---|
ensemblid | ENSG00000164953.17 |
hgncid | 28396 |
symbol | TMEM67 |
name | transmembrane protein 67 |
refseq_nuc | NM_153704.6 |
refseq_prot | NP_714915.3 |
ensembl_nuc | ENST00000453321.8 |
ensembl_prot | ENSP00000389998.3 |
mane_status | MANE Select |
chr | chr8 |
start | 93754894 |
end | 93818121 |
strand | + |
ver | v1.2 |
region | chr8:93754894-93818121 |
region5000 | chr8:93749894-93823121 |
regionname0 | TMEM67_chr8_93754894_93818121 |
regionname5000 | TMEM67_chr8_93749894_93823121 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 995 | 202 | 70 | 40 | 66 | 4 | 21 | 57 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002 | 1/0 | 995 | 110 | 20 | 23 | 45 | 8 | 13 | 40 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0003 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0004 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0005 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0006 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0007 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0008 | 0/0 | 995 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2988 | 176 | 67 | 35 | 51 | 4 | 18 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0002 | 1/0 | 2988 | 108 | 20 | 23 | 44 | 8 | 12 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0003 | 0/0 | 2988 | 22 | 0 | 4 | 15 | 0 | 3 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0004 | 0/0 | 2988 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0005 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0006 | 0/0 | 2988 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0007 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0008 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0009 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0010 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0011 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
c0012 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1691 | 299 | 78 | 61 | 114 | 11 | 33 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0002 | 0/0 | 1691 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0003 | 0/0 | 1691 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0004 | 0/0 | 1691 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0005 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0006 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0007 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0008 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0009 | 0/0 | 1691 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
t0010 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2988 | 176 | 67 | 35 | 51 | 4 | 18 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0003 | 0/0 | 2988 | 22 | 0 | 4 | 15 | 0 | 3 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0004 | 0/0 | 2988 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0002 | 1/0 | 2988 | 108 | 20 | 23 | 44 | 8 | 12 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0008 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0009 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0003c0005 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0004c0007 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0005c0010 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0006c0011 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0007c0012 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0008c0006 | 0/0 | 2988 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4678 | 164 | 56 | 34 | 51 | 4 | 18 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0001t0002 | 0/0 | 4678 | 7 | 6 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0001t0003 | 0/0 | 4678 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0001t0006 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0001t0007 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0003t0001 | 0/0 | 4678 | 22 | 0 | 4 | 15 | 0 | 3 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0001c0004t0001 | 0/0 | 4678 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0002t0001 | 1/0 | 4678 | 103 | 19 | 21 | 44 | 7 | 11 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0002t0004 | 0/0 | 4678 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0002t0005 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0002t0008 | 0/0 | 4678 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0002t0009 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0008t0001 | 0/0 | 4678 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0002c0009t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0003c0005t0010 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0004c0007t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0005c0010t0002 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0006c0011t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0007c0012t0001 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
a0008c0006t0001 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | copy fasta | chr8 | 93749894 | 93823121 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0004t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0008g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0002t0009g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0008t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0002c0009t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0003c0005t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0004c0007t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0005c0010t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0006c0011t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0007c0012t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
a0008c0006t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | CHS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00741 | hp1 | a0002 | c0002 | t0004 | g0092 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01109 | hp2 | a0002 | c0002 | t0009 | g0124 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01167 | hp2 | a0001 | c0004 | t0001 | g0095 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0253 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01243 | hp2 | a0008 | c0006 | t0001 | g0227 | AMR | PUR | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0141 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0238 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0012 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0012 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0237 | EUR | IBS | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0223 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | KHV | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02451 | hp2 | a0003 | c0005 | t0010 | g0064 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0123 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02647 | hp2 | a0002 | c0002 | t0005 | g0080 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0222 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02723 | hp2 | a0005 | c0010 | t0002 | g0065 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02738 | hp2 | a0002 | c0002 | t0008 | g0119 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0131 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ESN | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0109 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0165 | SAS | BEB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0190 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0249 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | STU | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18949 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18978 | hp1 | a0006 | c0011 | t0001 | g0278 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18981 | hp1 | a0007 | c0012 | t0001 | g0106 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19056 | hp2 | a0002 | c0009 | t0001 | g0017 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0224 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19076 | hp2 | a0004 | c0007 | t0001 | g0218 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19078 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0196 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20752 | hp2 | a0002 | c0002 | t0004 | g0118 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0281 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20905 | hp2 | a0002 | c0008 | t0001 | g0081 | SAS | GIH | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | USA | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0200 | REF | REF | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0103 | REF | REF | TMEM67_chr8_93749894_93823121 | TMEM67 | chr8 | 93749894 | 93823121 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:93754939
|
G | A | 1 | a0003 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.25G>A | p.Val9Met | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/28 | 46/4678 | 25/2988 | 9/995 | chr8 | 93754939 | ||
chr8:93780659
|
G | A | 1 | a0008 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.781G>A | p.Asp261Asn | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/28 | 802/4678 | 781/2988 | 261/995 | chr8 | 93780659 | ||
chr8:93780684
|
G | T | 1 | a0007 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.806G>T | p.Gly269Val | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/28 | 827/4678 | 806/2988 | 269/995 | chr8 | 93780684 | ||
chr8:93780885
|
T | A | 1 | a0004 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.881T>A | p.Leu294His | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/28 | 902/4678 | 881/2988 | 294/995 | chr8 | 93780885 | ||
chr8:93795937
|
A | G | 6 | a0001a0003a0004others(3): Show | 207 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
missense_variant | MODERATE | c.1810A>G | p.Ile604Val | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/28 | 1831/4678 | 1810/2988 | 604/995 | chr8 | 93795937 | ||
chr8:93799684
|
T | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2167T>C | p.Tyr723His | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/28 | 2188/4678 | 2167/2988 | 723/995 | chr8 | 93799684 | ||
chr8:93816388
|
G | A | 1 | a0006 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.2924G>A | p.Arg975His | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 2945/4678 | 2924/2988 | 975/995 | chr8 | 93816388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:93804836
|
T | C | 1 | a0002c0008 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.2397T>C | p.Asp799Asp | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/28 | 2418/4678 | 2397/2988 | 799/995 | chr8 | 93804836 | ||
chr8:93809793
|
G | A | 1 | a0002c0009 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.2670G>A | p.Lys890Lys | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/28 | 2691/4678 | 2670/2988 | 890/995 | chr8 | 93809793 | ||
chr8:93815432
|
A | C | 1 | a0001c0003 | 22 | HG00673.hp1 HG01192.hp2 HG01928.hp2 others(19): Show |
synonymous_variant | LOW | c.2892A>C | p.Thr964Thr | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/28 | 2913/4678 | 2892/2988 | 964/995 | chr8 | 93815432 | ||
chr8:93816416
|
A | G | 1 | a0001c0004 | 4 | HG01167.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.2952A>G | p.Ala984Ala | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 2973/4678 | 2952/2988 | 984/995 | chr8 | 93816416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:93816471
|
T | C | 2 | a0001c0001t0002a0005c0010t0002 | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*19T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 19 | chr8 | 93816471 | |||||
chr8:93816511
|
A | T | 1 | a0003c0005t0010 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 59 | chr8 | 93816511 | |||||
chr8:93816993
|
A | C | 1 | a0002c0002t0009 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 541 | chr8 | 93816993 | |||||
chr8:93817059
|
T | C | 1 | a0002c0002t0005 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 607 | chr8 | 93817059 | |||||
chr8:93817132
|
G | A | 1 | a0001c0001t0006 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 680 | chr8 | 93817132 | |||||
chr8:93817190
|
G | T | 1 | a0002c0002t0008 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 738 | chr8 | 93817190 | |||||
chr8:93817304
|
C | T | 1 | a0001c0001t0003 | 3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*852C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 852 | chr8 | 93817304 | |||||
chr8:93817986
|
G | A | 1 | a0001c0001t0007 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1534G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 1534 | chr8 | 93817986 | |||||
chr8:93818105
|
G | A | 1 | a0002c0002t0004 | 2 | HG00741.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1653G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 28/28 | 1653 | chr8 | 93818105 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:93755202
|
C | G | 2 | a0002c0002t0001g0294a0002c0002t0001g0295 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.223+65C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | chr8 | 93755202 | ||||||
chr8:93755210
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.223+73G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | chr8 | 93755210 | ||||||
chr8:93755696
|
A | T | 1 | a0002c0002t0001g0293 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.224-82A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | chr8 | 93755696 | ||||||
chr8:93755751
|
C | CT | 19 | a0001c0001t0001g0275a0001c0001t0001g0279a0001c0001t0001g0282others(16): Show | 19 | HG00408.hp2 HG00673.hp1 HG00741.hp2 others(16): Show |
splice_acceptor_variant&intron_variant | HIGH | c.224-3dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 93755751 | |||||
chr8:93755751
|
CT | C | 42 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 43 | HG01070.hp1 HG01070.hp2 HG01261.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.224-3delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 93755751 | |||||
chr8:93755751
|
CTTT | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0019others(2): Show | 7 | HG01255.hp1 HG01358.hp1 HG01993.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.224-5_224-3delTTT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 93755751 | |||||
chr8:93755896
|
C | G | 3 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0292 | 3 | HG00597.hp2 NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.312+30C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93755896 | ||||||
chr8:93756060
|
T | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+194T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756060 | ||||||
chr8:93756125
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+259G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756125 | ||||||
chr8:93756238
|
C | T | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+372C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756238 | ||||||
chr8:93756278
|
T | A | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+412T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756278 | ||||||
chr8:93756385
|
A | T | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.312+519A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756385 | ||||||
chr8:93756461
|
GTC | G | 6 | a0002c0002t0001g0017a0002c0002t0001g0056a0002c0002t0001g0264others(3): Show | 6 | NA18977.hp2 NA18984.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+597_312+598del others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93756461 | |||||
chr8:93756565
|
A | G | 5 | a0002c0002t0001g0259a0002c0002t0001g0260a0002c0002t0001g0261others(2): Show | 5 | NA18961.hp1 NA18977.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.312+699A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756565 | ||||||
chr8:93756612
|
C | G | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.312+746C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756612 | ||||||
chr8:93756697
|
C | A | 1 | a0002c0002t0001g0272 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.312+831C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756697 | ||||||
chr8:93756699
|
A | G | 1 | a0002c0002t0001g0258 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.312+833A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756699 | ||||||
chr8:93756708
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.312+842A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756708 | ||||||
chr8:93756926
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.312+1060G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93756926 | ||||||
chr8:93757004
|
G | A | 4 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072others(1): Show | 4 | HG00733.hp1 HG01258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+1138G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757004 | ||||||
chr8:93757018
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+1152A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757018 | ||||||
chr8:93757090
|
T | TATAA | 26 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 29 | HG00673.hp2 HG01070.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.312+1263_312+1266d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | |||||
chr8:93757090
|
TATAA | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 105 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.312+1263_312+1266d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | |||||
chr8:93757090
|
TATAAATA others(1): Show |
T | 89 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(86): Show | 92 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.312+1259_312+1266d others(10): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | |||||
chr8:93757090
|
TATAAATA others(5): Show |
T | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.312+1255_312+1266d others(14): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757090 | |||||
chr8:93757239
|
C | G | 17 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.313-1244C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757239 | ||||||
chr8:93757251
|
C | T | 1 | a0001c0003t0001g0253 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.313-1232C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757251 | ||||||
chr8:93757320
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.313-1163T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757320 | ||||||
chr8:93757478
|
A | G | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-1005A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757478 | ||||||
chr8:93757635
|
C | CA | 15 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0042others(12): Show | 15 | HG00597.hp2 HG00741.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.313-835dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757635 | |||||
chr8:93757647
|
A | G | 1 | a0002c0002t0001g0007 | 2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.313-836A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93757647 | ||||||
chr8:93757766
|
AT | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-703delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93757766 | |||||
chr8:93758021
|
G | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027 | 3 | HG01261.hp2 HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.313-462G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93758021 | ||||||
chr8:93758067
|
G | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-416G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93758067 | ||||||
chr8:93758147
|
TTTGTG | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 6 | HG00140.hp1 HG01192.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-323_313-319del others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 93758147 | |||||
chr8:93758387
|
C | G | 14 | a0002c0002t0001g0012a0002c0002t0001g0015a0002c0002t0001g0052others(11): Show | 16 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.313-96C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 2/27 | chr8 | 93758387 | ||||||
chr8:93758933
|
A | AT | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+359dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93758933 | |||||
chr8:93758937
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+361A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93758937 | ||||||
chr8:93758964
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+388G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93758964 | ||||||
chr8:93759091
|
G | C | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.406+515G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759091 | ||||||
chr8:93759152
|
T | G | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.406+576T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759152 | ||||||
chr8:93759302
|
T | TA | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.406+737dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759302 | |||||
chr8:93759465
|
G | GA | 33 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(30): Show | 34 | HG00597.hp1 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.406+908dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759465 | |||||
chr8:93759619
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.406+1043C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759619 | ||||||
chr8:93759646
|
T | A | 1 | a0001c0001t0001g0019 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.406+1070T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759646 | ||||||
chr8:93759653
|
G | GT | 12 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(9): Show | 13 | HG02145.hp2 HG02922.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+1090dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759653 | |||||
chr8:93759653
|
GT | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0142a0001c0001t0001g0144others(4): Show | 8 | HG01981.hp1 HG02148.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.406+1090delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759653 | |||||
chr8:93759710
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.406+1134G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759710 | ||||||
chr8:93759920
|
A | AT | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1345dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759920 | |||||
chr8:93759937
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0030others(12): Show | 19 | HG00140.hp2 HG01081.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.406+1361C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759937 | ||||||
chr8:93759955
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1379G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93759955 | ||||||
chr8:93759978
|
A | ATAAT | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1404_406+1407d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93759978 | |||||
chr8:93760039
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.406+1463G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760039 | ||||||
chr8:93760049
|
T | G | 4 | a0001c0001t0001g0203a0001c0001t0001g0209a0001c0003t0001g0208others(1): Show | 4 | HG04184.hp1 NA18974.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+1473T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760049 | ||||||
chr8:93760149
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 100 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.406+1573G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760149 | ||||||
chr8:93760281
|
C | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.406+1705C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760281 | ||||||
chr8:93760359
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1783A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760359 | ||||||
chr8:93760677
|
C | CA | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 121 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.406+2111dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93760677 | |||||
chr8:93760810
|
G | A | 1 | a0002c0002t0001g0100 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.406+2234G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93760810 | ||||||
chr8:93761046
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 100 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.406+2470C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761046 | ||||||
chr8:93761107
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.406+2531C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761107 | ||||||
chr8:93761121
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.406+2545C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761121 | ||||||
chr8:93761156
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 127 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.406+2580T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761156 | ||||||
chr8:93761235
|
G | A | 1 | a0002c0002t0001g0101 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.407-2607G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761235 | ||||||
chr8:93761359
|
G | A | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.407-2483G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761359 | ||||||
chr8:93761562
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0038 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.407-2280G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761562 | ||||||
chr8:93761723
|
T | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-2119T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761723 | ||||||
chr8:93761750
|
A | G | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.407-2092A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761750 | ||||||
chr8:93761974
|
G | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0254others(3): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-1868G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761974 | ||||||
chr8:93761993
|
G | A | 6 | a0001c0001t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(3): Show | 6 | NA18967.hp2 NA18982.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-1849G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93761993 | ||||||
chr8:93762021
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.407-1821G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762021 | ||||||
chr8:93762041
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.407-1801G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762041 | ||||||
chr8:93762052
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.407-1790C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762052 | ||||||
chr8:93762184
|
A | G | 26 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(23): Show | 27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.407-1658A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762184 | ||||||
chr8:93762210
|
C | T | 76 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(73): Show | 78 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.407-1632C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762210 | ||||||
chr8:93762218
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.407-1624T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762218 | ||||||
chr8:93762268
|
A | G | 1 | a0002c0002t0001g0281 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.407-1574A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762268 | ||||||
chr8:93762340
|
CT | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-1489delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93762340 | |||||
chr8:93762365
|
AT | A | 28 | a0001c0001t0001g0093a0001c0001t0002g0022a0001c0001t0002g0023others(25): Show | 30 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.407-1466delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93762365 | |||||
chr8:93762386
|
G | T | 1 | a0002c0002t0001g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.407-1456G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762386 | ||||||
chr8:93762388
|
G | T | 1 | a0002c0002t0001g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.407-1454G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762388 | ||||||
chr8:93762827
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.407-1015G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762827 | ||||||
chr8:93762829
|
A | G | 1 | a0002c0002t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.407-1013A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762829 | ||||||
chr8:93762947
|
CAG | C | 18 | a0001c0001t0001g0075a0001c0001t0001g0127a0002c0002t0001g0007others(15): Show | 19 | HG00673.hp2 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.407-894_407-893del others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93762947 | ||||||
chr8:93763096
|
AT | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.407-733delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr8 | 93763096 | |||||
chr8:93763109
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.407-733T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93763109 | ||||||
chr8:93763570
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-272C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93763570 | ||||||
chr8:93763636
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(3): Show | 6 | HG02970.hp2 HG03453.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-206T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 3/27 | chr8 | 93763636 | ||||||
chr8:93763959
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0069 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.506+18G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93763959 | ||||||
chr8:93763989
|
G | A | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.506+48G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93763989 | ||||||
chr8:93764497
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.506+556G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93764497 | ||||||
chr8:93764501
|
A | AACAC | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(5): Show | 9 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.506+581_506+584dup others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 93764501 | |||||
chr8:93764501
|
AAC | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.506+583_506+584del others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 93764501 | |||||
chr8:93764754
|
T | G | 1 | a0002c0002t0009g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.507-652T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93764754 | ||||||
chr8:93765387
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.507-19T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 4/27 | chr8 | 93765387 | ||||||
chr8:93765774
|
A | G | 3 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0292 | 3 | HG00597.hp2 NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.651+128A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765774 | ||||||
chr8:93765779
|
CATT | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0107others(3): Show | 6 | NA18948.hp1 NA18961.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+135_651+137del others(3): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93765779 | |||||
chr8:93765827
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.651+181C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765827 | ||||||
chr8:93765955
|
G | A | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+309G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765955 | ||||||
chr8:93765963
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.651+317A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93765963 | ||||||
chr8:93766016
|
T | C | 1 | a0001c0001t0006g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.651+370T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766016 | ||||||
chr8:93766021
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.651+375T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766021 | ||||||
chr8:93766126
|
T | A | 3 | a0001c0001t0001g0132a0001c0004t0001g0008a0001c0004t0001g0131 | 4 | HG01167.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+480T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766126 | ||||||
chr8:93766149
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.651+503A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766149 | ||||||
chr8:93766204
|
A | G | 1 | a0002c0002t0005g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.651+558A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766204 | ||||||
chr8:93766226
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.651+580C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766226 | ||||||
chr8:93766265
|
C | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.651+619C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766265 | ||||||
chr8:93766343
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.651+697C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766343 | ||||||
chr8:93766367
|
G | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 149 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.651+721G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766367 | ||||||
chr8:93766385
|
T | G | 12 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(9): Show | 12 | HG01070.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.651+739T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93766385 | ||||||
chr8:93767087
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.651+1441C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767087 | ||||||
chr8:93767547
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.651+1901G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767547 | ||||||
chr8:93767722
|
G | A | 68 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0099others(65): Show | 69 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.651+2076G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767722 | ||||||
chr8:93767724
|
GA | G | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.651+2079delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767724 | ||||||
chr8:93767725
|
A | AT | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.651+2095dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767725 | |||||
chr8:93767725
|
A | ATT | 8 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0068others(5): Show | 9 | HG00597.hp1 HG01192.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+2094_651+2095d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767725 | |||||
chr8:93767725
|
A | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0254others(3): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+2079A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767725 | ||||||
chr8:93767725
|
AT | A | 12 | a0001c0001t0001g0075a0002c0002t0001g0007a0002c0002t0001g0076others(9): Show | 13 | HG00673.hp2 HG01952.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.651+2095delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767725 | |||||
chr8:93767777
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.651+2131T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767777 | ||||||
chr8:93767863
|
CT | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0060others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+2236delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767863 | |||||
chr8:93767863
|
CTT | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 208 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+2235_651+2236d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93767863 | |||||
chr8:93767870
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.651+2224T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767870 | ||||||
chr8:93767882
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.651+2236T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767882 | ||||||
chr8:93767983
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+2337C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93767983 | ||||||
chr8:93768238
|
C | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+2592C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768238 | ||||||
chr8:93768279
|
TACAC | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.651+2641_651+2644d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93768279 | |||||
chr8:93768315
|
T | C | 1 | a0005c0010t0002g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.651+2669T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768315 | ||||||
chr8:93768491
|
A | AT | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+2845_651+2846i others(3): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768491 | ||||||
chr8:93768612
|
A | AAAAATAA others(3): Show |
1 | a0001c0001t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.651+2978_651+2987d others(12): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93768612 | |||||
chr8:93768798
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.651+3152C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768798 | ||||||
chr8:93768947
|
A | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+3301A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768947 | ||||||
chr8:93768994
|
C | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+3348C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768994 | ||||||
chr8:93768995
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.651+3349G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93768995 | ||||||
chr8:93769160
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.652-3429G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769160 | ||||||
chr8:93769186
|
G | T | 1 | a0002c0002t0001g0084 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.652-3403G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769186 | ||||||
chr8:93769214
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0069 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.652-3375A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769214 | ||||||
chr8:93769249
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0177a0001c0001t0001g0180 | 3 | NA18950.hp1 NA18955.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.652-3340C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769249 | ||||||
chr8:93769334
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-3255G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769334 | ||||||
chr8:93769439
|
T | C | 1 | a0002c0002t0001g0192 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.652-3150T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769439 | ||||||
chr8:93769459
|
C | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 14 | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-3130C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769459 | ||||||
chr8:93769519
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.652-3070C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769519 | ||||||
chr8:93769752
|
G | A | 19 | a0002c0002t0001g0012a0002c0002t0001g0015a0002c0002t0001g0035others(16): Show | 21 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.652-2837G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769752 | ||||||
chr8:93769812
|
T | G | 1 | a0002c0002t0001g0111 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.652-2777T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769812 | ||||||
chr8:93769949
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0254others(3): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-2640A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93769949 | ||||||
chr8:93770051
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.652-2538C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770051 | ||||||
chr8:93770222
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.652-2367A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770222 | ||||||
chr8:93770239
|
C | T | 2 | a0002c0002t0001g0137a0002c0002t0001g0191 | 2 | HG02451.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.652-2350C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770239 | ||||||
chr8:93770423
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.652-2166A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770423 | ||||||
chr8:93770503
|
G | A | 68 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0099others(65): Show | 69 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.652-2086G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770503 | ||||||
chr8:93770740
|
C | T | 1 | a0001c0003t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.652-1849C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93770740 | ||||||
chr8:93771013
|
C | CA | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-1561dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93771013 | |||||
chr8:93771013
|
CA | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.652-1561delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93771013 | |||||
chr8:93771118
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.652-1471T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771118 | ||||||
chr8:93771249
|
C | CT | 9 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0002g0023others(6): Show | 9 | HG01074.hp1 HG01106.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-1328dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93771249 | |||||
chr8:93771261
|
T | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0055a0001c0001t0001g0105others(2): Show | 5 | HG02630.hp1 HG02976.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-1328T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771261 | ||||||
chr8:93771262
|
A | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.652-1327A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771262 | ||||||
chr8:93771293
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.652-1296T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771293 | ||||||
chr8:93771773
|
AG | A | 7 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-815delG | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771773 | ||||||
chr8:93771902
|
G | A | 2 | a0001c0001t0003g0006a0001c0001t0003g0189 | 3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.652-687G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771902 | ||||||
chr8:93771944
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.652-645G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93771944 | ||||||
chr8:93772038
|
C | CTG | 3 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0292 | 3 | HG00597.hp2 NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.652-549_652-548dup others(2): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr8 | 93772038 | |||||
chr8:93772401
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.652-188A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 6/27 | chr8 | 93772401 | ||||||
chr8:93772669
|
A | T | 1 | a0001c0001t0006g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.714+18A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93772669 | ||||||
chr8:93773066
|
G | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+415G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773066 | ||||||
chr8:93773324
|
G | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG00140.hp2 HG02258.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+673G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773324 | ||||||
chr8:93773341
|
C | T | 26 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(23): Show | 27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.714+690C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773341 | ||||||
chr8:93773744
|
T | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+1093T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773744 | ||||||
chr8:93773991
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.714+1340T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93773991 | ||||||
chr8:93774025
|
AT | A | 9 | a0001c0001t0001g0254a0001c0001t0002g0022a0001c0001t0002g0023others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+1387delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr8 | 93774025 | |||||
chr8:93774100
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.714+1449C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774100 | ||||||
chr8:93774281
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0254others(3): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+1630C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774281 | ||||||
chr8:93774293
|
G | T | 1 | a0001c0003t0001g0210 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.714+1642G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774293 | ||||||
chr8:93774500
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.714+1849A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774500 | ||||||
chr8:93774551
|
C | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.714+1900C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774551 | ||||||
chr8:93774573
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+1922C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774573 | ||||||
chr8:93774661
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.714+2010A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774661 | ||||||
chr8:93774773
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+2122G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774773 | ||||||
chr8:93774810
|
C | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.714+2159C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93774810 | ||||||
chr8:93775056
|
G | C | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.714+2405G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775056 | ||||||
chr8:93775111
|
T | C | 1 | a0002c0002t0001g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.714+2460T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775111 | ||||||
chr8:93775120
|
T | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0090 | 4 | HG01884.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2469T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775120 | ||||||
chr8:93775445
|
G | A | 3 | a0001c0001t0001g0127a0002c0002t0001g0096a0002c0002t0001g0126 | 3 | HG01981.hp2 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.714+2794G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775445 | ||||||
chr8:93775612
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.714+2961C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775612 | ||||||
chr8:93775785
|
A | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.714+3134A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775785 | ||||||
chr8:93775834
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.714+3183A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775834 | ||||||
chr8:93775840
|
T | G | 1 | a0001c0003t0001g0222 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.714+3189T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93775840 | ||||||
chr8:93776238
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 168 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.714+3587A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776238 | ||||||
chr8:93776265
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.714+3614G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776265 | ||||||
chr8:93776537
|
G | A | 1 | a0002c0002t0001g0276 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.714+3886G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776537 | ||||||
chr8:93776610
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+3959T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776610 | ||||||
chr8:93776716
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0090 | 4 | HG01884.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-3877T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776716 | ||||||
chr8:93776726
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.715-3867T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776726 | ||||||
chr8:93776727
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.715-3866T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776727 | ||||||
chr8:93776824
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.715-3769G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776824 | ||||||
chr8:93776960
|
G | A | 2 | a0002c0002t0001g0294a0002c0002t0001g0295 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.715-3633G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93776960 | ||||||
chr8:93777003
|
C | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-3590C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777003 | ||||||
chr8:93777233
|
C | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 168 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.715-3360C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777233 | ||||||
chr8:93777453
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 168 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.715-3140G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777453 | ||||||
chr8:93777481
|
T | C | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-3112T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777481 | ||||||
chr8:93777486
|
A | C | 1 | a0002c0002t0001g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.715-3107A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777486 | ||||||
chr8:93777687
|
T | A | 17 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.715-2906T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777687 | ||||||
chr8:93777729
|
C | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-2864C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777729 | ||||||
chr8:93777799
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715-2794C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777799 | ||||||
chr8:93777847
|
G | A | 3 | a0001c0001t0001g0127a0002c0002t0001g0096a0002c0002t0001g0126 | 3 | HG01981.hp2 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.715-2746G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777847 | ||||||
chr8:93777872
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.715-2721T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777872 | ||||||
chr8:93777972
|
T | A | 3 | a0002c0002t0001g0070a0002c0002t0001g0112a0002c0002t0001g0128 | 3 | HG00733.hp1 HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.715-2621T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777972 | ||||||
chr8:93777995
|
T | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18972.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.715-2598T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93777995 | ||||||
chr8:93778039
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.715-2554G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778039 | ||||||
chr8:93778182
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0019others(2): Show | 7 | HG01255.hp1 HG01358.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-2411T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778182 | ||||||
chr8:93778236
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.715-2357C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778236 | ||||||
chr8:93778241
|
G | A | 1 | a0001c0003t0001g0186 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.715-2352G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778241 | ||||||
chr8:93778309
|
T | G | 2 | a0002c0002t0001g0035a0002c0002t0001g0047 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.715-2284T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778309 | ||||||
chr8:93778450
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.715-2143T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778450 | ||||||
chr8:93778522
|
C | G | 3 | a0002c0002t0001g0070a0002c0002t0001g0112a0002c0002t0001g0128 | 3 | HG00733.hp1 HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.715-2071C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778522 | ||||||
chr8:93778556
|
T | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-2037T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778556 | ||||||
chr8:93778644
|
C | G | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1949C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778644 | ||||||
chr8:93778644
|
C | T | 2 | a0002c0002t0001g0110a0002c0002t0001g0120 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.715-1949C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778644 | ||||||
chr8:93778945
|
G | T | 1 | a0001c0001t0002g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715-1648G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93778945 | ||||||
chr8:93779038
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.715-1555A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779038 | ||||||
chr8:93779168
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-1425C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779168 | ||||||
chr8:93779191
|
T | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.715-1402T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779191 | ||||||
chr8:93779192
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.715-1401C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779192 | ||||||
chr8:93779287
|
C | T | 2 | a0002c0002t0001g0108a0007c0012t0001g0106 | 2 | NA18948.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.715-1306C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779287 | ||||||
chr8:93779403
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.715-1190T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779403 | ||||||
chr8:93779426
|
G | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0056a0002c0002t0001g0264others(3): Show | 6 | NA18977.hp2 NA18984.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1167G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779426 | ||||||
chr8:93779544
|
G | A | 1 | a0002c0002t0001g0113 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.715-1049G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93779544 | ||||||
chr8:93780046
|
C | G | 27 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0099others(24): Show | 27 | HG00408.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.715-547C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780046 | ||||||
chr8:93780046
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715-547C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780046 | ||||||
chr8:93780162
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0038 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.715-431G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780162 | ||||||
chr8:93780173
|
C | T | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-420C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780173 | ||||||
chr8:93780475
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715-118G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780475 | ||||||
chr8:93780535
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.715-58A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | chr8 | 93780535 | ||||||
chr8:93780548
|
CTGTTCAG others(5): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.715-40_715-29delCA others(10): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr8 | 93780548 | |||||
chr8:93780844
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0002g0063 | 3 | HG03195.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.870-30C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/27 | chr8 | 93780844 | ||||||
chr8:93780845
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0055others(4): Show | 7 | HG01070.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-29A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 8/27 | chr8 | 93780845 | ||||||
chr8:93781193
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.978+211A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781193 | ||||||
chr8:93781378
|
T | C | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.979-280T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781378 | ||||||
chr8:93781426
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.979-232A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781426 | ||||||
chr8:93781494
|
T | C | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.979-164T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781494 | ||||||
chr8:93781498
|
GT | G | 17 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.979-159delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781498 | ||||||
chr8:93781551
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-107A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 9/27 | chr8 | 93781551 | ||||||
chr8:93781826
|
G | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(1): Show | 6 | HG01255.hp1 HG01358.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065+82G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93781826 | ||||||
chr8:93781895
|
TTTTG | T | 2 | a0001c0001t0003g0006a0001c0001t0003g0189 | 3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1065+175_1065+178d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 93781895 | |||||
chr8:93781926
|
C | CT | 15 | a0002c0002t0001g0012a0002c0002t0001g0015a0002c0002t0001g0052others(12): Show | 17 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1065+192dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 93781926 | |||||
chr8:93781926
|
C | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065+182C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93781926 | ||||||
chr8:93781926
|
CT | C | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+192delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 93781926 | |||||
chr8:93781927
|
T | C | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065+183T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93781927 | ||||||
chr8:93782005
|
G | A | 9 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG01070.hp2 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1065+261G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782005 | ||||||
chr8:93782047
|
G | T | 1 | a0007c0012t0001g0106 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1065+303G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782047 | ||||||
chr8:93782070
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1066-325C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782070 | ||||||
chr8:93782221
|
A | T | 1 | a0004c0007t0001g0218 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1066-174A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782221 | ||||||
chr8:93782368
|
T | A | 1 | a0007c0012t0001g0106 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1066-27T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782368 | ||||||
chr8:93782392
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
splice_region_variant&intron_variant | LOW | c.1066-3C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 10/27 | chr8 | 93782392 | ||||||
chr8:93782561
|
T | G | 1 | a0007c0012t0001g0106 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1131+101T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782561 | ||||||
chr8:93782571
|
G | GT | 11 | a0001c0001t0001g0029a0001c0001t0001g0152a0001c0003t0001g0186others(8): Show | 12 | HG01081.hp1 HG01109.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131+130dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 93782571 | |||||
chr8:93782571
|
GT | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0145a0001c0001t0001g0234others(11): Show | 14 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1131+130delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 93782571 | |||||
chr8:93782577
|
T | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1131+117T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782577 | ||||||
chr8:93782730
|
C | G | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1131+270C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782730 | ||||||
chr8:93782834
|
C | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+374C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782834 | ||||||
chr8:93782835
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0003c0005t0010g0064 | 3 | HG00738.hp1 HG01099.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1131+375G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782835 | ||||||
chr8:93782864
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131+404C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782864 | ||||||
chr8:93782875
|
G | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131+415G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782875 | ||||||
chr8:93782908
|
T | G | 1 | a0001c0001t0001g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1131+448T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93782908 | ||||||
chr8:93783196
|
C | T | 4 | a0001c0001t0001g0127a0002c0002t0001g0096a0002c0002t0001g0126others(1): Show | 4 | HG01981.hp2 HG04115.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131+736C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783196 | ||||||
chr8:93783282
|
G | A | 1 | a0002c0002t0001g0258 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1131+822G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783282 | ||||||
chr8:93783288
|
G | A | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1131+828G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783288 | ||||||
chr8:93783451
|
C | T | 1 | a0001c0001t0006g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1131+991C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783451 | ||||||
chr8:93783496
|
T | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | NA18968.hp2 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1131+1036T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783496 | ||||||
chr8:93783817
|
A | AG | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131+1357_1131+135 others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783817 | ||||||
chr8:93783831
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1131+1371T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783831 | ||||||
chr8:93783893
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1132-1329G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93783893 | ||||||
chr8:93784029
|
C | A | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1132-1193C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784029 | ||||||
chr8:93784376
|
G | A | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132-846G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784376 | ||||||
chr8:93784421
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-801G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784421 | ||||||
chr8:93784498
|
A | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1132-724A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784498 | ||||||
chr8:93784584
|
C | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0285 | 2 | HG00408.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1132-638C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784584 | ||||||
chr8:93784745
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1132-477A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784745 | ||||||
chr8:93784860
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1132-362G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 11/27 | chr8 | 93784860 | ||||||
chr8:93785424
|
C | T | 26 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(23): Show | 27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1288+46C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785424 | ||||||
chr8:93785660
|
G | A | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1288+282G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785660 | ||||||
chr8:93785744
|
G | A | 2 | a0002c0002t0001g0076a0002c0002t0001g0274 | 2 | NA18967.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1288+366G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785744 | ||||||
chr8:93785801
|
C | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1289-422C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785801 | ||||||
chr8:93785811
|
C | T | 1 | a0002c0002t0001g0172 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1289-412C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 12/27 | chr8 | 93785811 | ||||||
chr8:93786456
|
G | A | 1 | a0005c0010t0002g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1412+110G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93786456 | ||||||
chr8:93786547
|
G | A | 12 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(9): Show | 12 | HG01070.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412+201G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93786547 | ||||||
chr8:93786637
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1412+291G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93786637 | ||||||
chr8:93787197
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1413-647G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787197 | ||||||
chr8:93787301
|
T | A | 1 | a0001c0003t0001g0223 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1413-543T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787301 | ||||||
chr8:93787409
|
G | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0090 | 4 | HG01884.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413-435G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787409 | ||||||
chr8:93787625
|
A | G | 2 | a0002c0002t0001g0171a0002c0002t0001g0233 | 2 | NA18954.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1413-219A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 13/27 | chr8 | 93787625 | ||||||
chr8:93787967
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1518+18T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93787967 | ||||||
chr8:93788031
|
G | A | 2 | a0002c0002t0001g0110a0002c0002t0001g0120 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1518+82G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788031 | ||||||
chr8:93788033
|
CT | C | 10 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(7): Show | 10 | HG01261.hp2 HG01515.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1518+98delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93788033 | |||||
chr8:93788219
|
T | C | 1 | a0001c0001t0006g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1518+270T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788219 | ||||||
chr8:93788423
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1518+474C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788423 | ||||||
chr8:93788495
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0038 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1518+546G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788495 | ||||||
chr8:93788649
|
A | C | 2 | a0002c0002t0001g0197a0002c0002t0001g0198 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1518+700A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788649 | ||||||
chr8:93788890
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1518+941A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788890 | ||||||
chr8:93788941
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1518+992G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788941 | ||||||
chr8:93788984
|
T | C | 14 | a0002c0002t0001g0012a0002c0002t0001g0015a0002c0002t0001g0052others(11): Show | 16 | HG01081.hp1 HG01106.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1518+1035T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93788984 | ||||||
chr8:93789094
|
T | C | 1 | a0002c0002t0001g0183 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1518+1145T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789094 | ||||||
chr8:93789098
|
T | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0254others(3): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1518+1149T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789098 | ||||||
chr8:93789130
|
A | G | 5 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | HG01934.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1518+1181A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789130 | ||||||
chr8:93789281
|
C | T | 1 | a0002c0002t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1518+1332C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789281 | ||||||
chr8:93789497
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1518+1548C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789497 | ||||||
chr8:93789523
|
T | C | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1518+1574T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789523 | ||||||
chr8:93789651
|
AAT | A | 21 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0055others(18): Show | 21 | HG00738.hp2 HG01070.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1519-1593_1519-159 others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93789651 | |||||
chr8:93789653
|
T | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 192 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1519-1610T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789653 | ||||||
chr8:93789655
|
T | A | 31 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0033others(28): Show | 32 | HG01070.hp2 HG01261.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.1519-1608T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789655 | ||||||
chr8:93789667
|
TA | T | 188 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(185): Show | 200 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1519-1595delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789667 | ||||||
chr8:93789668
|
A | T | 1 | a0001c0001t0001g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1519-1595A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789668 | ||||||
chr8:93789669
|
TA | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(42): Show | 50 | HG00140.hp1 HG01192.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1519-1593delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789669 | ||||||
chr8:93789670
|
A | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(210): Show | 228 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1519-1593A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789670 | ||||||
chr8:93789670
|
AT | A | 12 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0074others(9): Show | 13 | HG01261.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1519-1583delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93789670 | |||||
chr8:93789672
|
T | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0255 | 3 | HG02717.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1519-1591T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789672 | ||||||
chr8:93789691
|
A | C | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1519-1572A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789691 | ||||||
chr8:93789790
|
G | T | 1 | a0002c0002t0008g0119 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1519-1473G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789790 | ||||||
chr8:93789797
|
G | A | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519-1466G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789797 | ||||||
chr8:93789804
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1519-1459C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789804 | ||||||
chr8:93789947
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1519-1316A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93789947 | ||||||
chr8:93790070
|
GA | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1519-1182delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr8 | 93790070 | |||||
chr8:93790076
|
A | G | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1519-1187A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790076 | ||||||
chr8:93790084
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1519-1179C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790084 | ||||||
chr8:93790140
|
T | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1519-1123T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790140 | ||||||
chr8:93790318
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1519-945C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790318 | ||||||
chr8:93790572
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1519-691A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790572 | ||||||
chr8:93790575
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1519-688A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790575 | ||||||
chr8:93790645
|
T | C | 1 | a0002c0002t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1519-618T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790645 | ||||||
chr8:93790697
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1519-566C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790697 | ||||||
chr8:93790801
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0217a0001c0001t0001g0286others(1): Show | 4 | HG00597.hp1 NA18946.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519-462C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 14/27 | chr8 | 93790801 | ||||||
chr8:93791372
|
G | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(23): Show | 27 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1575+53G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791372 | ||||||
chr8:93791387
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1575+68A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791387 | ||||||
chr8:93791669
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1575+350G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791669 | ||||||
chr8:93791829
|
C | T | 1 | a0002c0002t0001g0015 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1575+510C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791829 | ||||||
chr8:93791939
|
G | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1575+620G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93791939 | ||||||
chr8:93792050
|
T | G | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1575+731T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792050 | ||||||
chr8:93792101
|
A | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1575+782A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792101 | ||||||
chr8:93792120
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01070.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+801C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792120 | ||||||
chr8:93792313
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1576-885G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792313 | ||||||
chr8:93792388
|
G | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-810G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792388 | ||||||
chr8:93792478
|
A | G | 2 | a0002c0002t0001g0272a0002c0002t0001g0292 | 2 | NA18949.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1576-720A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792478 | ||||||
chr8:93792562
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1576-636C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792562 | ||||||
chr8:93792599
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1576-599A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792599 | ||||||
chr8:93792691
|
A | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-507A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792691 | ||||||
chr8:93792773
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1576-425C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792773 | ||||||
chr8:93792773
|
CT | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0039others(11): Show | 15 | HG01516.hp1 HG02280.hp1 HG02922.hp2 others(12): Show |
intron_variant | MODIFIER | c.1576-410delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr8 | 93792773 | |||||
chr8:93792831
|
C | T | 2 | a0002c0002t0001g0035a0002c0002t0001g0047 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1576-367C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792831 | ||||||
chr8:93792962
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1576-236C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792962 | ||||||
chr8:93792973
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1576-225G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792973 | ||||||
chr8:93792974
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1576-224T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792974 | ||||||
chr8:93792984
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1576-214G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792984 | ||||||
chr8:93792985
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1576-213A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93792985 | ||||||
chr8:93793017
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1576-181T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93793017 | ||||||
chr8:93793023
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1576-175G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93793023 | ||||||
chr8:93793114
|
G | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-84G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 15/27 | chr8 | 93793114 | ||||||
chr8:93793326
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1674+30T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793326 | ||||||
chr8:93793390
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1674+94G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793390 | ||||||
chr8:93793421
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1674+125G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793421 | ||||||
chr8:93793886
|
T | G | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1674+590T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93793886 | ||||||
chr8:93794036
|
C | T | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+740C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794036 | ||||||
chr8:93794097
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1674+801G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794097 | ||||||
chr8:93794166
|
A | G | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1674+870A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794166 | ||||||
chr8:93794427
|
G | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675-982G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794427 | ||||||
chr8:93794530
|
G | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1675-879G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794530 | ||||||
chr8:93794629
|
G | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1675-780G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794629 | ||||||
chr8:93794667
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1675-742G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794667 | ||||||
chr8:93794728
|
T | C | 19 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(16): Show | 19 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675-681T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93794728 | ||||||
chr8:93795021
|
C | T | 1 | a0002c0002t0001g0295 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1675-388C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93795021 | ||||||
chr8:93795023
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675-386A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93795023 | ||||||
chr8:93795212
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1675-197G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 16/27 | chr8 | 93795212 | ||||||
chr8:93795517
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1773+10T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795517 | ||||||
chr8:93795583
|
T | C | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1773+76T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795583 | ||||||
chr8:93795768
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1774-133G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795768 | ||||||
chr8:93795811
|
C | CA | 12 | a0001c0001t0001g0062a0001c0001t0001g0132a0001c0001t0001g0267others(9): Show | 13 | HG01167.hp1 HG01167.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1774-81dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr8 | 93795811 | |||||
chr8:93795828
|
G | A | 4 | a0002c0002t0001g0052a0002c0002t0001g0193a0002c0002t0001g0194others(1): Show | 4 | HG02738.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774-73G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795828 | ||||||
chr8:93795856
|
A | C | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0003c0005t0010g0064 | 3 | HG01261.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1774-45A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 17/27 | chr8 | 93795856 | ||||||
chr8:93796339
|
G | A | 2 | a0001c0001t0002g0063a0003c0005t0010g0064 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1860+352G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796339 | ||||||
chr8:93796340
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0254others(3): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1860+353A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796340 | ||||||
chr8:93796405
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1860+418T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796405 | ||||||
chr8:93796500
|
T | C | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1860+513T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796500 | ||||||
chr8:93796589
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1861-545G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796589 | ||||||
chr8:93796627
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1861-507G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796627 | ||||||
chr8:93796658
|
C | T | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1861-476C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796658 | ||||||
chr8:93796720
|
G | A | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1861-414G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796720 | ||||||
chr8:93796957
|
C | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1861-177C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93796957 | ||||||
chr8:93797067
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1861-67A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 18/27 | chr8 | 93797067 | ||||||
chr8:93797652
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2100+182T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93797652 | ||||||
chr8:93797708
|
A | G | 6 | a0001c0001t0001g0097a0002c0002t0001g0100a0002c0002t0001g0111others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2100+238A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93797708 | ||||||
chr8:93797865
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2100+395C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93797865 | ||||||
chr8:93798282
|
CTA | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0068 | 3 | HG01070.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2100+814_2100+815d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798282 | |||||
chr8:93798942
|
A | AGT | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 99 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.2101-635_2101-634d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
A | AGTGT | 26 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0046others(23): Show | 27 | HG01070.hp2 HG01243.hp2 HG02293.hp2 others(24): Show |
intron_variant | MODIFIER | c.2101-637_2101-634d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
A | AGTGTGT | 12 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0055others(9): Show | 12 | HG01243.hp1 HG01261.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2101-639_2101-634d others(8): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0059others(4): Show | 7 | HG02717.hp1 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2101-641_2101-634d others(10): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0220 | 3 | HG01884.hp2 HG01978.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2101-643_2101-634d others(12): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
AGT | A | 48 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0001t0001g0105others(45): Show | 53 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.2101-635_2101-634d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
AGTGT | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0107a0001c0001t0002g0022others(15): Show | 18 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2101-637_2101-634d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
AGTGTGT | A | 28 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(25): Show | 31 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.2101-639_2101-634d others(8): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0153 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2101-643_2101-634d others(12): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798942
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2101-645_2101-634d others(14): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798942 | |||||
chr8:93798983
|
GT | G | 3 | a0001c0001t0001g0075a0002c0002t0001g0079a0002c0002t0001g0082 | 3 | HG02004.hp1 NA19001.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2101-632delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 93798983 | |||||
chr8:93798984
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2101-634_2101-633i others(13): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93798984 | ||||||
chr8:93799070
|
C | A | 1 | a0005c0010t0002g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2101-548C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93799070 | ||||||
chr8:93799425
|
A | C | 12 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(9): Show | 12 | HG01070.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2101-193A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93799425 | ||||||
chr8:93799452
|
T | C | 44 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0001g0102others(41): Show | 49 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2101-166T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 20/27 | chr8 | 93799452 | ||||||
chr8:93799870
|
A | G | 1 | a0002c0002t0001g0101 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2241+112A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93799870 | ||||||
chr8:93799904
|
C | CTT | 8 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0050others(5): Show | 9 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+166_2241+167d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93799904 | |||||
chr8:93799904
|
CT | C | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 191 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2241+167delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93799904 | |||||
chr8:93799904
|
CTTT | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+165_2241+167d others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93799904 | |||||
chr8:93800421
|
G | A | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2241+663G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800421 | ||||||
chr8:93800431
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2241+673G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800431 | ||||||
chr8:93800508
|
A | G | 2 | a0002c0002t0001g0123a0007c0012t0001g0106 | 2 | HG02622.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2241+750A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800508 | ||||||
chr8:93800753
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2241+995C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800753 | ||||||
chr8:93800764
|
T | C | 3 | a0002c0002t0001g0141a0002c0002t0001g0197a0002c0002t0001g0198 | 3 | HG01257.hp2 HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2241+1006T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800764 | ||||||
chr8:93800781
|
C | G | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2241+1023C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800781 | ||||||
chr8:93800850
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0239 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2241+1092A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800850 | ||||||
chr8:93800864
|
A | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2241+1106A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93800864 | ||||||
chr8:93801047
|
G | T | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2241+1289G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801047 | ||||||
chr8:93801071
|
A | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+1313A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801071 | ||||||
chr8:93801216
|
A | G | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.2241+1458A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801216 | ||||||
chr8:93801218
|
T | C | 1 | a0002c0008t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2241+1460T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801218 | ||||||
chr8:93801306
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2241+1548T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801306 | ||||||
chr8:93801400
|
A | AT | 16 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0074others(13): Show | 16 | HG01123.hp1 HG01169.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1660dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93801400 | |||||
chr8:93801400
|
AT | A | 32 | a0001c0001t0001g0019a0001c0001t0001g0054a0001c0001t0001g0086others(29): Show | 32 | HG00408.hp2 HG00597.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.2241+1660delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93801400 | |||||
chr8:93801433
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2241+1675C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801433 | ||||||
chr8:93801620
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2241+1862A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801620 | ||||||
chr8:93801828
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2242-1776A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93801828 | ||||||
chr8:93802193
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2242-1411T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802193 | ||||||
chr8:93802196
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2242-1408C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802196 | ||||||
chr8:93802222
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2242-1382C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802222 | ||||||
chr8:93802232
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2242-1372A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93802232 | ||||||
chr8:93802324
|
ATCT | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG00140.hp2 HG02258.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2242-1275_2242-127 others(7): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr8 | 93802324 | |||||
chr8:93803161
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2242-443C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803161 | ||||||
chr8:93803275
|
A | G | 1 | a0002c0002t0001g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2242-329A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803275 | ||||||
chr8:93803420
|
C | T | 6 | a0001c0003t0001g0053a0001c0003t0001g0186a0001c0003t0001g0207others(3): Show | 6 | HG01192.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242-184C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803420 | ||||||
chr8:93803431
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2242-173C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803431 | ||||||
chr8:93803526
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2242-78T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803526 | ||||||
chr8:93803573
|
T | C | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2242-31T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803573 | ||||||
chr8:93803576
|
T | C | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2242-28T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 21/27 | chr8 | 93803576 | ||||||
chr8:93803879
|
AT | A | 10 | a0001c0001t0001g0134a0001c0001t0001g0157a0001c0001t0001g0211others(7): Show | 10 | HG00733.hp2 HG01099.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2322+210delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93803879 | |||||
chr8:93803879
|
ATTT | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2322+208_2322+210d others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93803879 | |||||
chr8:93803911
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2322+227A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93803911 | ||||||
chr8:93804148
|
A | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2322+464A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804148 | ||||||
chr8:93804169
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 76 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2322+485G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804169 | ||||||
chr8:93804298
|
C | CTCTTT | 16 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0132others(13): Show | 16 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2323-452_2323-448d others(7): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804298 | |||||
chr8:93804310
|
C | CT | 21 | a0001c0001t0001g0029a0001c0001t0001g0075a0001c0001t0001g0127others(18): Show | 23 | HG00673.hp2 HG01109.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.2323-430dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | |||||
chr8:93804310
|
C | CTTTT | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2323-433_2323-430d others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | |||||
chr8:93804310
|
CT | C | 25 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0050others(22): Show | 26 | HG01099.hp1 HG01243.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.2323-430delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | |||||
chr8:93804310
|
CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0055others(4): Show | 7 | HG01070.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2323-440_2323-430d others(13): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804310 | |||||
chr8:93804311
|
T | TTTTC | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 140 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2323-448_2323-447i others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804311 | |||||
chr8:93804312
|
T | TTTC | 10 | a0001c0001t0001g0038a0001c0001t0001g0158a0001c0001t0001g0209others(7): Show | 10 | HG01109.hp1 HG01167.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2323-448_2323-447i others(5): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804312 | |||||
chr8:93804366
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2323-396C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804366 | ||||||
chr8:93804381
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 167 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.2323-381C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804381 | ||||||
chr8:93804481
|
A | AT | 30 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(27): Show | 34 | HG00140.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.2323-261dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr8 | 93804481 | |||||
chr8:93804518
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG01070.hp2 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2323-244C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804518 | ||||||
chr8:93804548
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2323-214C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804548 | ||||||
chr8:93804595
|
A | C | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2323-167A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 22/27 | chr8 | 93804595 | ||||||
chr8:93804929
|
T | A | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2439+51T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93804929 | ||||||
chr8:93804949
|
T | A | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2439+71T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93804949 | ||||||
chr8:93805126
|
C | T | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2439+248C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805126 | ||||||
chr8:93805350
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2439+472G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805350 | ||||||
chr8:93805446
|
T | A | 1 | a0001c0004t0001g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2439+568T>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805446 | ||||||
chr8:93805447
|
G | T | 1 | a0001c0004t0001g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2439+569G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805447 | ||||||
chr8:93805453
|
G | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0034 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2439+575G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805453 | ||||||
chr8:93805580
|
C | CA | 11 | a0001c0001t0001g0033a0001c0001t0001g0055a0001c0001t0001g0098others(8): Show | 11 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2439+720dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93805580 | |||||
chr8:93805580
|
CA | C | 21 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0090others(18): Show | 22 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.2439+720delA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93805580 | |||||
chr8:93805630
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2439+752A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805630 | ||||||
chr8:93805946
|
G | C | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2439+1068G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93805946 | ||||||
chr8:93806113
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2439+1235C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806113 | ||||||
chr8:93806146
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2439+1268T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806146 | ||||||
chr8:93806190
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2439+1312G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806190 | ||||||
chr8:93806356
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2439+1478G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806356 | ||||||
chr8:93806405
|
G | A | 9 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG01070.hp2 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1527G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806405 | ||||||
chr8:93806850
|
A | C | 2 | a0002c0002t0001g0112a0002c0002t0001g0128 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2439+1972A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806850 | ||||||
chr8:93806857
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2439+1979T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93806857 | ||||||
chr8:93807103
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2440-1737T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807103 | ||||||
chr8:93807113
|
T | G | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2440-1727T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807113 | ||||||
chr8:93807445
|
T | C | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-1395T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807445 | ||||||
chr8:93807618
|
A | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2440-1222A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807618 | ||||||
chr8:93807738
|
A | G | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2440-1102A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807738 | ||||||
chr8:93807874
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2440-966A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807874 | ||||||
chr8:93807885
|
A | G | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2440-955A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807885 | ||||||
chr8:93807887
|
A | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-953A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807887 | ||||||
chr8:93807949
|
G | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-891G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93807949 | ||||||
chr8:93808130
|
A | C | 4 | a0002c0002t0001g0017a0002c0002t0001g0056a0002c0002t0001g0266others(1): Show | 4 | NA18984.hp2 NA19010.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-710A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808130 | ||||||
chr8:93808257
|
T | C | 1 | a0002c0002t0001g0192 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2440-583T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808257 | ||||||
chr8:93808338
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2440-502A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808338 | ||||||
chr8:93808368
|
A | ATCTACTA others(33): Show |
1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2440-463_2440-462i others(42): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808368 | |||||
chr8:93808374
|
T | C | 1 | a0002c0002t0009g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2440-466T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808374 | ||||||
chr8:93808378
|
A | T | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.2440-462A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808378 | ||||||
chr8:93808443
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG00741.hp2 HG02004.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-397T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808443 | ||||||
chr8:93808458
|
T | C | 3 | a0001c0001t0001g0127a0002c0002t0001g0096a0002c0002t0001g0126 | 3 | HG01981.hp2 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2440-382T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808458 | ||||||
chr8:93808464
|
T | TATCTATT others(32): Show |
170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 183 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.2440-373_2440-335d others(41): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(49): Show |
1 | a0002c0002t0001g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(58): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(60): Show |
1 | a0001c0001t0001g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2440-335_2440-334i others(69): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(127): Show |
6 | a0001c0001t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(3): Show | 6 | NA18967.hp2 NA18982.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(136): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(88): Show |
1 | a0002c0002t0001g0113 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(97): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(105): Show |
1 | a0002c0002t0001g0196 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2440-335_2440-334i others(114): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(105): Show |
14 | a0002c0002t0001g0012a0002c0002t0001g0052a0002c0002t0001g0137others(11): Show | 15 | HG01106.hp2 HG01255.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(114): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(133): Show |
1 | a0002c0002t0001g0015 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2440-335_2440-334i others(142): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(211): Show |
1 | a0002c0002t0001g0276 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(220): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(183): Show |
1 | a0002c0002t0001g0182 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(192): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(155): Show |
11 | a0001c0003t0001g0287a0002c0002t0001g0035a0002c0002t0001g0036others(8): Show | 11 | HG00597.hp2 HG01891.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(164): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(127): Show |
48 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0001g0102others(45): Show | 53 | HG00558.hp2 HG00673.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(136): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(166): Show |
1 | a0002c0002t0001g0037 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2440-335_2440-334i others(175): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(123): Show |
2 | a0002c0002t0001g0110a0002c0002t0001g0120 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2440-335_2440-334i others(132): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(99): Show |
2 | a0002c0002t0001g0129a0002c0002t0009g0124 | 2 | HG01109.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.2440-335_2440-334i others(108): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(71): Show |
18 | a0001c0001t0001g0016a0001c0001t0001g0074a0001c0001t0001g0088others(15): Show | 19 | HG00140.hp2 HG01081.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(80): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808464
|
T | TATCTATT others(68): Show |
1 | a0001c0001t0001g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2440-366_2440-365i others(77): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808464 | |||||
chr8:93808480
|
T | TTATCTAT others(17): Show |
1 | a0002c0002t0001g0007 | 2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2440-350_2440-349i others(26): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808480 | |||||
chr8:93808484
|
C | CTATAATA others(28): Show |
11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2440-335_2440-334i others(37): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr8 | 93808484 | |||||
chr8:93808505
|
T | TATTTATC others(170): Show |
1 | a0002c0002t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-335_2440-334i others(179): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808505 | ||||||
chr8:93808506
|
G | T | 1 | a0002c0002t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-334G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808506 | ||||||
chr8:93808518
|
T | C | 1 | a0002c0002t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-322T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808518 | ||||||
chr8:93808529
|
A | G | 19 | a0001c0001t0001g0075a0001c0001t0001g0127a0002c0002t0001g0007others(16): Show | 20 | HG00673.hp2 HG00733.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2440-311A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808529 | ||||||
chr8:93808547
|
T | C | 1 | a0002c0002t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2440-293T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808547 | ||||||
chr8:93808594
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0069 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2440-246G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808594 | ||||||
chr8:93808599
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0245 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2440-241G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808599 | ||||||
chr8:93808610
|
G | T | 1 | a0002c0002t0001g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2440-230G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808610 | ||||||
chr8:93808834
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG04115.hp1 | splice_region_variant&intron_variant | LOW | c.2440-6T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 23/27 | chr8 | 93808834 | ||||||
chr8:93809203
|
A | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2661+42A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809203 | ||||||
chr8:93809297
|
T | G | 1 | a0001c0001t0001g0286 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2661+136T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809297 | ||||||
chr8:93809422
|
A | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2661+261A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809422 | ||||||
chr8:93809511
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2662-274T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809511 | ||||||
chr8:93809517
|
T | C | 1 | a0002c0002t0001g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2662-268T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809517 | ||||||
chr8:93809549
|
A | G | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2662-236A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809549 | ||||||
chr8:93809574
|
C | A | 1 | a0002c0002t0001g0079 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2662-211C>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809574 | ||||||
chr8:93809643
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0043others(16): Show | 21 | HG00408.hp1 HG00558.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.2662-142G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809643 | ||||||
chr8:93809685
|
A | G | 3 | a0001c0001t0001g0048a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG01928.hp1 HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2662-100A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 25/27 | chr8 | 93809685 | ||||||
chr8:93809971
|
CT | C | 13 | a0001c0001t0001g0211a0001c0001t0001g0255a0001c0001t0002g0022others(10): Show | 13 | HG01167.hp2 HG01261.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.2764+100delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93809971 | |||||
chr8:93809987
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2764+100T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93809987 | ||||||
chr8:93809991
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2764+104C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93809991 | ||||||
chr8:93810026
|
T | C | 1 | a0002c0002t0001g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2764+139T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810026 | ||||||
chr8:93810036
|
T | C | 1 | a0001c0003t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2764+149T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810036 | ||||||
chr8:93810126
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2764+239G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810126 | ||||||
chr8:93810181
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2764+294G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810181 | ||||||
chr8:93810259
|
A | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.2764+372A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93810259 | ||||||
chr8:93811043
|
T | C | 1 | a0003c0005t0010g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2764+1156T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811043 | ||||||
chr8:93811325
|
GCAAAGAC | G | 67 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0054others(64): Show | 68 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.2764+1439_2764+144 others(11): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811325 | ||||||
chr8:93811335
|
T | C | 67 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0054others(64): Show | 68 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.2764+1448T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811335 | ||||||
chr8:93811337
|
A | C | 67 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0054others(64): Show | 68 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.2764+1450A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811337 | ||||||
chr8:93811344
|
C | G | 17 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2764+1457C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811344 | ||||||
chr8:93811586
|
G | A | 3 | a0002c0002t0001g0108a0002c0002t0001g0258a0007c0012t0001g0106 | 3 | NA18948.hp1 NA18981.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2764+1699G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811586 | ||||||
chr8:93811663
|
A | G | 1 | a0001c0003t0001g0230 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2764+1776A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811663 | ||||||
chr8:93811785
|
G | T | 2 | a0002c0002t0001g0110a0002c0002t0001g0120 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2764+1898G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811785 | ||||||
chr8:93811794
|
G | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2764+1907G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811794 | ||||||
chr8:93811906
|
T | G | 1 | a0002c0002t0001g0037 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2764+2019T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93811906 | ||||||
chr8:93812056
|
G | A | 3 | a0001c0004t0001g0008a0001c0004t0001g0095a0001c0004t0001g0131 | 4 | HG01167.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2764+2169G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812056 | ||||||
chr8:93812089
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2764+2202T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812089 | ||||||
chr8:93812108
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2764+2221C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812108 | ||||||
chr8:93812149
|
C | CA | 11 | a0001c0001t0001g0242a0001c0001t0002g0022a0001c0001t0002g0023others(8): Show | 11 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2764+2278dupA | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93812149 | |||||
chr8:93812377
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2764+2490G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812377 | ||||||
chr8:93812704
|
G | T | 1 | a0002c0002t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2765-2601G>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812704 | ||||||
chr8:93812991
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2765-2314C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93812991 | ||||||
chr8:93813149
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2765-2156C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93813149 | ||||||
chr8:93813247
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2765-2058C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93813247 | ||||||
chr8:93813596
|
A | T | 2 | a0002c0002t0001g0085a0002c0002t0005g0080 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2765-1709A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93813596 | ||||||
chr8:93814135
|
C | CTTT | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01261.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2765-1150_2765-114 others(7): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814135 | |||||
chr8:93814135
|
CT | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 278 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.2765-1148delT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814135 | |||||
chr8:93814135
|
CTT | C | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0166others(7): Show | 10 | HG01099.hp2 HG02273.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2765-1149_2765-114 others(6): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814135 | |||||
chr8:93814163
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02717.hp2 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2765-1142G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814163 | ||||||
chr8:93814239
|
A | G | 1 | a0001c0003t0001g0224 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2765-1066A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814239 | ||||||
chr8:93814296
|
T | C | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2765-1009T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814296 | ||||||
chr8:93814299
|
G | C | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2765-1006G>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814299 | ||||||
chr8:93814300
|
T | C | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2765-1005T>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814300 | ||||||
chr8:93814385
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2765-920C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814385 | ||||||
chr8:93814438
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2765-867A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814438 | ||||||
chr8:93814468
|
G | GT | 6 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0254others(3): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2765-828dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814468 | |||||
chr8:93814469
|
T | G | 1 | a0001c0001t0001g0216 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2765-836T>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814469 | ||||||
chr8:93814523
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2765-782C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814523 | ||||||
chr8:93814566
|
A | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2765-739A>C | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814566 | ||||||
chr8:93814568
|
G | A | 1 | a0001c0003t0001g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2765-737G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814568 | ||||||
chr8:93814630
|
C | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 168 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.2765-675C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93814630 | ||||||
chr8:93814652
|
C | CT | 7 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0066others(4): Show | 7 | HG00673.hp2 HG01070.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2765-638dupT | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814652 | |||||
chr8:93814652
|
C | CTT | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2765-639_2765-638d others(4): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr8 | 93814652 | |||||
chr8:93815246
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2765-59A>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 26/27 | chr8 | 93815246 | ||||||
chr8:93815772
|
C | T | 1 | a0008c0006t0001g0227 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2907+325C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93815772 | ||||||
chr8:93815829
|
A | AAGGGAAG others(8): Show |
182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 195 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.2907+384_2907+385i others(17): Show |
TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr8 | 93815829 | |||||
chr8:93815854
|
C | G | 1 | a0001c0001t0002g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2907+407C>G | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93815854 | ||||||
chr8:93816315
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2908-57G>A | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93816315 | ||||||
chr8:93816329
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2908-43C>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93816329 | ||||||
chr8:93816337
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2908-35A>T | TMEM67 | ENSG00000164953.17 | transcript | ENST00000453321.8 | protein_coding | 27/27 | chr8 | 93816337 |