geneid | 54960 |
---|---|
ensemblid | ENSG00000046647.14 |
hgncid | 26044 |
symbol | GEMIN8 |
name | gem nuclear organelle associated protein 8 |
refseq_nuc | NM_001042479.2 |
refseq_prot | NP_001035944.1 |
ensembl_nuc | ENST00000680255.1 |
ensembl_prot | ENSP00000505429.1 |
mane_status | MANE Select |
chr | chrX |
start | 14006726 |
end | 14029892 |
strand | - |
ver | v1.2 |
region | chrX:14006726-14029892 |
region5000 | chrX:14001726-14034892 |
regionname0 | GEMIN8_chrX_14006726_14029892 |
regionname5000 | GEMIN8_chrX_14001726_14034892 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 242 | 251 | 71 | 53 | 89 | 9 | 27 | 68 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0002 | 0/0 | 242 | 19 | 0 | 2 | 16 | 0 | 1 | 14 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0003 | 0/0 | 242 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0004 | 0/0 | 186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 729 | 249 | 69 | 53 | 89 | 9 | 27 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
c0002 | 0/0 | 729 | 19 | 0 | 2 | 16 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
c0003 | 0/0 | 729 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
c0004 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
c0005 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
c0006 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2419 | 190 | 34 | 37 | 88 | 8 | 21 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0002 | 0/0 | 2419 | 53 | 14 | 15 | 15 | 1 | 8 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0003 | 0/0 | 2419 | 8 | 8 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0004 | 0/0 | 2419 | 8 | 7 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0005 | 0/0 | 2419 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0006 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0007 | 0/0 | 2419 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0008 | 0/0 | 2419 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0009 | 0/0 | 2419 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0010 | 0/0 | 2419 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0011 | 0/0 | 2419 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0012 | 0/0 | 2419 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0013 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0014 | 0/0 | 2419 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
t0015 | 0/0 | 2419 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/1 | 20 | 0 | 4 | 12 | 1 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0002 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0004 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0006 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0009 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0014 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 729 | 249 | 69 | 53 | 89 | 9 | 27 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0005 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0006 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0002c0002 | 0/0 | 729 | 19 | 0 | 2 | 16 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0003c0003 | 0/0 | 729 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0004c0004 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3147 | 188 | 34 | 37 | 88 | 8 | 19 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0002 | 0/0 | 3147 | 34 | 13 | 13 | 0 | 1 | 7 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0003 | 0/0 | 3147 | 8 | 8 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0004 | 0/0 | 3147 | 7 | 6 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0005 | 0/0 | 3147 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0008 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0009 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0010 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0011 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0012 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0013 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0014 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0001t0015 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0005t0004 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0001c0006t0002 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0002c0002t0002 | 0/0 | 3147 | 18 | 0 | 2 | 15 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0002c0002t0007 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0003c0003t0001 | 0/0 | 3147 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
a0004c0004t0006 | 0/0 | 3223 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | copy fasta | chrX | 14001726 | 14034892 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/1 | 20 | 0 | 4 | 12 | 1 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0014 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0004 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0009 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0004g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0012g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0014g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0001t0015g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0005t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0001c0006t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0002c0002t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
a0004c0004t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | FIN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00733 | hp1 | a0001 | c0001 | t0015 | g0100 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01081 | hp1 | a0001 | c0001 | t0012 | g0127 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01884 | hp1 | a0001 | c0001 | t0013 | g0112 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0190 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0188 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0166 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0119 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0120 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03540 | hp1 | a0001 | c0005 | t0004 | g0177 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03579 | hp1 | a0001 | c0006 | t0002 | g0163 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03831 | hp2 | a0001 | c0001 | t0014 | g0041 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0192 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0054 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0116 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19010 | hp2 | a0002 | c0002 | t0007 | g0189 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19075 | hp1 | a0004 | c0004 | t0006 | g0099 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | ASW | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA21309 | hp1 | a0001 | c0001 | t0010 | g0183 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14006726
|
T | TA | 1 | a0004 | 1 | NA19075.hp1 | splice_region_variant | LOW | c.*2186dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | chrX | 14006726 | ||||||
chrX:14008956
|
C | CG | 1 | a0004 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.685dupC | p.Arg229fs | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 916/3147 | 685/729 | 229/242 | chrX | 14008956 | ||
chrX:14008995
|
T | TC | 1 | a0004 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.646dupG | p.Glu216fs | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 877/3147 | 646/729 | 216/242 | chrX | 14008995 | ||
chrX:14009011
|
T | TG | 1 | a0004 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.630dupC | p.Lys211fs | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 861/3147 | 630/729 | 210/242 | chrX | 14009011 | ||
chrX:14009022
|
T | TC | 1 | a0004 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.619dupG | p.Asp207fs | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 850/3147 | 619/729 | 207/242 | chrX | 14009022 | ||
chrX:14009058
|
T | A | 1 | a0002 | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
missense_variant | MODERATE | c.584A>T | p.Glu195Val | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 815/3147 | 584/729 | 195/242 | chrX | 14009058 | ||
chrX:14009094
|
C | CG | 1 | a0004 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.547dupC | p.Arg183fs | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 778/3147 | 547/729 | 183/242 | chrX | 14009094 | ||
chrX:14009099
|
G | GT | 1 | a0004 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.542dupA | p.Asn181fs | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 773/3147 | 542/729 | 181/242 | chrX | 14009099 | ||
chrX:14020459
|
C | A | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.91G>T | p.Ala31Ser | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/5 | 322/3147 | 91/729 | 31/242 | chrX | 14020459 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14009096
|
G | C | 1 | a0001c0005 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.546C>G | p.Thr182Thr | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 777/3147 | 546/729 | 182/242 | chrX | 14009096 | ||
chrX:14020415
|
G | C | 1 | a0001c0006 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.135C>G | p.Ala45Ala | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/5 | 366/3147 | 135/729 | 45/242 | chrX | 14020415 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14006734
|
T | TC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2178dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 2178 | chrX | 14006734 | |||||
chrX:14006739
|
A | AT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 2173 | chrX | 14006739 | |||||
chrX:14006805
|
T | TG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 2107 | chrX | 14006805 | |||||
chrX:14006883
|
T | TA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2029dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 2029 | chrX | 14006883 | |||||
chrX:14006938
|
A | AG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1974dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1974 | chrX | 14006938 | |||||
chrX:14006955
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1957dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1957 | chrX | 14006955 | |||||
chrX:14007025
|
T | TC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1887dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1887 | chrX | 14007025 | |||||
chrX:14007032
|
T | TTA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880_*1881insTA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1880 | chrX | 14007032 | |||||
chrX:14007033
|
A | T | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1880 | chrX | 14007033 | |||||
chrX:14007083
|
A | AT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1829dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1829 | chrX | 14007083 | |||||
chrX:14007115
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1797dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1797 | chrX | 14007115 | |||||
chrX:14007139
|
G | GGC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1773_*1774insGC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1773 | chrX | 14007139 | |||||
chrX:14007140
|
C | A | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1773G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1773 | chrX | 14007140 | |||||
chrX:14007187
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1725dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1725 | chrX | 14007187 | |||||
chrX:14007270
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1642dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1642 | chrX | 14007270 | |||||
chrX:14007339
|
G | GC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1573dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1573 | chrX | 14007339 | |||||
chrX:14007386
|
C | CT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1526dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1526 | chrX | 14007386 | |||||
chrX:14007457
|
A | AT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1455dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1455 | chrX | 14007457 | |||||
chrX:14007475
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1437dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1437 | chrX | 14007475 | |||||
chrX:14007489
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1423dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1423 | chrX | 14007489 | |||||
chrX:14007525
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1387dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1387 | chrX | 14007525 | |||||
chrX:14007542
|
C | CTT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369_*1370dupAA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1370 | chrX | 14007542 | |||||
chrX:14007542
|
CT | C | 1 | a0001c0001t0013 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1370delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1370 | chrX | 14007542 | |||||
chrX:14007543
|
T | C | 1 | a0001c0001t0005 | 4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1370A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1370 | chrX | 14007543 | |||||
chrX:14007564
|
T | TGGA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346_*1348dupTCC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1348 | chrX | 14007564 | |||||
chrX:14007567
|
A | G | 1 | a0001c0001t0012 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1346 | chrX | 14007567 | |||||
chrX:14007611
|
T | TC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1301dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1301 | chrX | 14007611 | |||||
chrX:14007677
|
G | A | 1 | a0001c0001t0003 | 8 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1236C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1236 | chrX | 14007677 | |||||
chrX:14007680
|
A | AC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1232 | chrX | 14007680 | |||||
chrX:14007688
|
C | T | 1 | a0001c0001t0014 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1225 | chrX | 14007688 | |||||
chrX:14007721
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1191 | chrX | 14007721 | |||||
chrX:14007803
|
A | AG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1109dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1109 | chrX | 14007803 | |||||
chrX:14007810
|
A | AG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1102dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1102 | chrX | 14007810 | |||||
chrX:14007818
|
C | T | 1 | a0001c0001t0011 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1095 | chrX | 14007818 | |||||
chrX:14007821
|
C | T | 1 | a0001c0001t0010 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1092G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1092 | chrX | 14007821 | |||||
chrX:14007826
|
C | CG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1086dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1086 | chrX | 14007826 | |||||
chrX:14007835
|
T | TTG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077_*1078insCA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1077 | chrX | 14007835 | |||||
chrX:14007836
|
G | T | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077C>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1077 | chrX | 14007836 | |||||
chrX:14007843
|
G | GC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1069 | chrX | 14007843 | |||||
chrX:14007863
|
T | TC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1049dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1049 | chrX | 14007863 | |||||
chrX:14007907
|
A | AG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1005 | chrX | 14007907 | |||||
chrX:14007944
|
C | CA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 968 | chrX | 14007944 | |||||
chrX:14007988
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 924 | chrX | 14007988 | |||||
chrX:14008013
|
C | CT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*899dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 899 | chrX | 14008013 | |||||
chrX:14008023
|
A | AG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*889dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 889 | chrX | 14008023 | |||||
chrX:14008037
|
T | TG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 875 | chrX | 14008037 | |||||
chrX:14008066
|
G | GC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 846 | chrX | 14008066 | |||||
chrX:14008075
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*837dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 837 | chrX | 14008075 | |||||
chrX:14008099
|
T | TC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 813 | chrX | 14008099 | |||||
chrX:14008146
|
A | AT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 766 | chrX | 14008146 | |||||
chrX:14008195
|
T | TCC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*717_*718insGG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 717 | chrX | 14008195 | |||||
chrX:14008248
|
A | C | 1 | a0001c0001t0009 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 665 | chrX | 14008248 | |||||
chrX:14008264
|
A | AT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 648 | chrX | 14008264 | |||||
chrX:14008268
|
C | A | 2 | a0001c0001t0004a0001c0005t0004 | 8 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*645G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 645 | chrX | 14008268 | |||||
chrX:14008272
|
C | T | 1 | a0001c0001t0008 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*641G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 641 | chrX | 14008272 | |||||
chrX:14008281
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 631 | chrX | 14008281 | |||||
chrX:14008292
|
T | TA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 620 | chrX | 14008292 | |||||
chrX:14008301
|
A | T | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 612 | chrX | 14008301 | |||||
chrX:14008302
|
T | A | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 611 | chrX | 14008302 | |||||
chrX:14008304
|
A | G | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*609T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 609 | chrX | 14008304 | |||||
chrX:14008305
|
G | A | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 608 | chrX | 14008305 | |||||
chrX:14008325
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 587 | chrX | 14008325 | |||||
chrX:14008398
|
T | C | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(5): Show | 67 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*515A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 515 | chrX | 14008398 | |||||
chrX:14008472
|
T | TG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*440dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 440 | chrX | 14008472 | |||||
chrX:14008485
|
A | G | 1 | a0001c0001t0003 | 8 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*428T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 428 | chrX | 14008485 | |||||
chrX:14008494
|
A | AT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 418 | chrX | 14008494 | |||||
chrX:14008502
|
T | TG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 410 | chrX | 14008502 | |||||
chrX:14008514
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 398 | chrX | 14008514 | |||||
chrX:14008539
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 373 | chrX | 14008539 | |||||
chrX:14008561
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 351 | chrX | 14008561 | |||||
chrX:14008589
|
T | TA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*323dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 323 | chrX | 14008589 | |||||
chrX:14008606
|
A | AG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*306dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 306 | chrX | 14008606 | |||||
chrX:14008640
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 272 | chrX | 14008640 | |||||
chrX:14008658
|
T | TA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 254 | chrX | 14008658 | |||||
chrX:14008680
|
C | CA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 232 | chrX | 14008680 | |||||
chrX:14008701
|
G | GA | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 211 | chrX | 14008701 | |||||
chrX:14008739
|
A | AC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 173 | chrX | 14008739 | |||||
chrX:14008822
|
G | A | 1 | a0001c0001t0015 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 91 | chrX | 14008822 | |||||
chrX:14008823
|
T | TC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 89 | chrX | 14008823 | |||||
chrX:14008838
|
A | G | 1 | a0002c0002t0007 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 75 | chrX | 14008838 | |||||
chrX:14008846
|
A | AG | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 66 | chrX | 14008846 | |||||
chrX:14008867
|
G | GT | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 45 | chrX | 14008867 | |||||
chrX:14008897
|
A | AC | 1 | a0004c0004t0006 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 15 | chrX | 14008897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14009174
|
G | GA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.473-6dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009174 | ||||||
chrX:14009190
|
G | GA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-22dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009190 | ||||||
chrX:14009196
|
G | GA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-28dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009196 | ||||||
chrX:14009236
|
T | TG | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-68dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009236 | ||||||
chrX:14009248
|
C | CT | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-80dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009248 | ||||||
chrX:14009314
|
G | GC | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-146dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009314 | ||||||
chrX:14009345
|
A | AT | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-177dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009345 | ||||||
chrX:14009394
|
G | GT | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-226dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009394 | ||||||
chrX:14009430
|
T | TG | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-262dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009430 | ||||||
chrX:14009474
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.473-305G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009474 | ||||||
chrX:14009562
|
A | AAG | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-394_473-393ins others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009562 | ||||||
chrX:14009563
|
G | A | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-394C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009563 | ||||||
chrX:14009621
|
A | AG | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-453dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009621 | ||||||
chrX:14009627
|
G | GA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-459dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009627 | ||||||
chrX:14009666
|
C | CT | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-498dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009666 | ||||||
chrX:14009705
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.473-536C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009705 | ||||||
chrX:14009761
|
C | CA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-593dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009761 | ||||||
chrX:14009780
|
T | TC | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-612dupG | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009780 | ||||||
chrX:14009829
|
G | GA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-661dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009829 | ||||||
chrX:14009853
|
G | GTT | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-685_473-684ins others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009853 | ||||||
chrX:14009874
|
G | GGA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-706_473-705ins others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009874 | ||||||
chrX:14009942
|
C | T | 2 | a0001c0001t0003g0053a0001c0001t0011g0054 | 2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.473-773G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009942 | ||||||
chrX:14009949
|
C | CA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-781dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009949 | ||||||
chrX:14009967
|
G | GA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-799dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009967 | ||||||
chrX:14009983
|
C | CA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-815dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009983 | ||||||
chrX:14010014
|
A | AG | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-846dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010014 | ||||||
chrX:14010028
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0101a0001c0001t0001g0152 | 4 | HG02004.hp1 HG02300.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-859T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010028 | ||||||
chrX:14010069
|
C | CA | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-901dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010069 | ||||||
chrX:14010093
|
G | GT | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-925dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010093 | ||||||
chrX:14010155
|
G | GT | 1 | a0004c0004t0006g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-987dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010155 | ||||||
chrX:14010526
|
G | A | 7 | a0001c0001t0002g0029a0001c0001t0002g0178a0001c0001t0002g0179others(4): Show | 12 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.473-1357C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010526 | ||||||
chrX:14010992
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0109others(2): Show | 6 | HG01884.hp1 HG02486.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.473-1823C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010992 | ||||||
chrX:14011043
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.473-1874G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011043 | ||||||
chrX:14011065
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.473-1896G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011065 | ||||||
chrX:14011516
|
C | CT | 25 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0066others(22): Show | 28 | HG00558.hp1 HG00639.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.473-2348dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
C | CTTTTTTT | 4 | a0001c0001t0001g0028a0001c0001t0001g0167a0001c0001t0003g0150others(1): Show | 5 | HG01884.hp2 HG02055.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-2354_473-2348d others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0165a0001c0001t0003g0026a0001c0001t0003g0053others(4): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-2355_473-2348d others(10): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473-2357_473-2348d others(12): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CT | C | 13 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0069others(10): Show | 14 | HG01081.hp1 HG01993.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-2348delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CTT | C | 1 | a0001c0001t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.473-2349_473-2348d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CTTTT | C | 23 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0016others(20): Show | 35 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-2351_473-2348d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CTTTTT | C | 3 | a0001c0001t0001g0148a0001c0001t0002g0039a0001c0001t0002g0042 | 3 | HG01169.hp2 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.473-2352_473-2348d others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CTTTTTTT | C | 1 | a0001c0001t0001g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.473-2354_473-2348d others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CTTTTTTT others(1): Show |
C | 1 | a0001c0001t0001g0157 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.473-2355_473-2348d others(10): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0061a0001c0001t0002g0008a0001c0001t0005g0027others(3): Show | 10 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.473-2358_473-2348d others(13): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011516
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.473-2360_473-2348d others(15): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | ||||||
chrX:14011827
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.473-2658T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011827 | ||||||
chrX:14012081
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.473-2912G>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012081 | ||||||
chrX:14012131
|
A | AT | 5 | a0001c0001t0001g0020a0001c0001t0001g0055a0001c0001t0001g0141others(2): Show | 6 | HG00323.hp1 HG01346.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-2963dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012131 | ||||||
chrX:14012131
|
AT | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0102a0001c0001t0001g0173 | 3 | HG02109.hp2 NA19003.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.473-2963delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012131 | ||||||
chrX:14012292
|
AT | A | 23 | a0001c0001t0001g0058a0001c0001t0001g0167a0001c0001t0001g0173others(20): Show | 33 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.473-3124delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012292 | ||||||
chrX:14012292
|
ATT | A | 24 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0016others(21): Show | 35 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-3125_473-3124d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012292 | ||||||
chrX:14012324
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.473-3155T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012324 | ||||||
chrX:14012403
|
C | T | 15 | a0001c0001t0001g0173a0002c0002t0002g0015a0002c0002t0002g0030others(12): Show | 20 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.473-3234G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012403 | ||||||
chrX:14012855
|
T | TA | 3 | a0001c0001t0005g0027a0001c0001t0005g0162a0001c0001t0005g0164 | 4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-3687dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012855 | ||||||
chrX:14012857
|
T | G | 3 | a0001c0001t0005g0027a0001c0001t0005g0162a0001c0001t0005g0164 | 4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-3688A>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012857 | ||||||
chrX:14012857
|
T | TG | 43 | a0001c0001t0001g0094a0001c0001t0001g0173a0001c0001t0002g0004others(40): Show | 63 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.473-3689dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012857 | ||||||
chrX:14013320
|
T | C | 1 | a0001c0001t0005g0164 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.473-4151A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013320 | ||||||
chrX:14013490
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0056others(5): Show | 12 | HG00558.hp1 HG02027.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.473-4321T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013490 | ||||||
chrX:14013508
|
G | C | 1 | a0001c0001t0001g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.473-4339C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013508 | ||||||
chrX:14013581
|
A | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0028others(28): Show | 36 | HG00558.hp1 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.473-4412T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013581 | ||||||
chrX:14013788
|
G | GT | 1 | a0001c0001t0001g0083 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.473-4620dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013788 | ||||||
chrX:14013788
|
GT | G | 47 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0078others(44): Show | 68 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.473-4620delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013788 | ||||||
chrX:14013788
|
GTT | G | 3 | a0001c0001t0002g0040a0001c0001t0005g0162a0002c0002t0002g0184 | 3 | HG01167.hp1 HG02897.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.473-4621_473-4620d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013788 | ||||||
chrX:14013882
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.473-4713G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013882 | ||||||
chrX:14013891
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.473-4722A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013891 | ||||||
chrX:14014024
|
G | GA | 2 | a0001c0001t0001g0104a0001c0001t0001g0147 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.473-4856dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014024 | ||||||
chrX:14014175
|
C | T | 61 | a0001c0001t0001g0028a0001c0001t0001g0148a0001c0001t0001g0165others(58): Show | 84 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.473-5006G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014175 | ||||||
chrX:14014179
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.473-5010A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014179 | ||||||
chrX:14014186
|
C | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0165a0001c0001t0001g0167others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.473-5017G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014186 | ||||||
chrX:14014361
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.473-5192G>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014361 | ||||||
chrX:14014497
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473-5328G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014497 | ||||||
chrX:14014824
|
TTGAG | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0056others(15): Show | 22 | HG00558.hp1 HG00639.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.472+5250_472+5253d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014824 | ||||||
chrX:14014838
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472+5240G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014838 | ||||||
chrX:14014932
|
C | T | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+5146G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014932 | ||||||
chrX:14015941
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.472+4137T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14015941 | ||||||
chrX:14015946
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.472+4132G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14015946 | ||||||
chrX:14015992
|
A | AG | 54 | a0001c0001t0001g0028a0001c0001t0001g0165a0001c0001t0001g0167others(51): Show | 76 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.472+4085dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14015992 | ||||||
chrX:14016054
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.472+4024T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016054 | ||||||
chrX:14016218
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.472+3860C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016218 | ||||||
chrX:14016572
|
G | A | 6 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0003g0149others(3): Show | 7 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.472+3506C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016572 | ||||||
chrX:14016573
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.472+3505G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016573 | ||||||
chrX:14016693
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.472+3385T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016693 | ||||||
chrX:14016844
|
C | CA | 9 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0105others(6): Show | 14 | HG00621.hp1 HG01175.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.472+3233dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016844
|
C | CAA | 2 | a0001c0001t0001g0106a0001c0001t0001g0113 | 2 | HG04115.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.472+3232_472+3233d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016844
|
CA | C | 11 | a0001c0001t0001g0058a0001c0001t0001g0069a0001c0001t0001g0082others(8): Show | 11 | HG00323.hp2 HG01099.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.472+3233delT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016844
|
CAA | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.472+3232_472+3233d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016844
|
CAAA | C | 1 | a0002c0002t0002g0186 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.472+3231_472+3233d others(5): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016844
|
CAAAAA | C | 2 | a0002c0002t0002g0031a0002c0002t0002g0187 | 3 | NA18969.hp2 NA19003.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.472+3229_472+3233d others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016844
|
CAAAAAAA | C | 7 | a0002c0002t0002g0015a0002c0002t0002g0032a0002c0002t0002g0050others(4): Show | 10 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.472+3227_472+3233d others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016844
|
CAAAAAAA others(2): Show |
C | 1 | a0002c0002t0002g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.472+3225_472+3233d others(11): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | ||||||
chrX:14016848
|
A | ATATAT | 1 | a0002c0002t0002g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.472+3229_472+3230i others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016848 | ||||||
chrX:14016848
|
A | ATATATAT | 2 | a0002c0002t0002g0030a0002c0002t0002g0184 | 3 | NA18939.hp1 NA18942.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.472+3229_472+3230i others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016848 | ||||||
chrX:14016850
|
A | T | 3 | a0002c0002t0002g0030a0002c0002t0002g0184a0002c0002t0002g0185 | 4 | NA18939.hp1 NA18942.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+3228T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016850 | ||||||
chrX:14016852
|
A | T | 4 | a0002c0002t0002g0030a0002c0002t0002g0184a0002c0002t0002g0185others(1): Show | 5 | NA18939.hp1 NA18942.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+3226T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016852 | ||||||
chrX:14016854
|
A | T | 6 | a0002c0002t0002g0030a0002c0002t0002g0031a0002c0002t0002g0184others(3): Show | 8 | NA18939.hp1 NA18942.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+3224T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016854 | ||||||
chrX:14016856
|
A | T | 13 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(10): Show | 18 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.472+3222T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016856 | ||||||
chrX:14016858
|
A | T | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3220T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016858 | ||||||
chrX:14016860
|
A | T | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3218T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016860 | ||||||
chrX:14016862
|
A | T | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3216T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016862 | ||||||
chrX:14016864
|
A | AAT | 3 | a0001c0001t0001g0012a0001c0001t0001g0089a0001c0001t0001g0126 | 5 | HG00735.hp1 HG02027.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+3213_472+3214i others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016864 | ||||||
chrX:14016864
|
A | T | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3214T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016864 | ||||||
chrX:14016864
|
AAAAT | A | 1 | a0001c0001t0002g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.472+3210_472+3213d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016864 | ||||||
chrX:14016864
|
AAAATAT | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0149 | 3 | HG02622.hp1 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.472+3208_472+3213d others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016864 | ||||||
chrX:14016865
|
AAAT | A | 1 | a0001c0001t0001g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.472+3210_472+3212d others(5): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016865 | ||||||
chrX:14016865
|
AAATAT | A | 6 | a0001c0001t0002g0038a0001c0001t0002g0178a0001c0001t0003g0074others(3): Show | 6 | HG01975.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+3208_472+3212d others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016865 | ||||||
chrX:14016866
|
A | AAAAT | 1 | a0001c0001t0001g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.472+3211_472+3212i others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | AAAT | 2 | a0001c0001t0001g0131a0001c0001t0002g0046 | 2 | HG01256.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.472+3211_472+3212i others(5): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | AAT | 18 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0056others(15): Show | 21 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.472+3210_472+3211d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | AATAT | 5 | a0001c0001t0001g0073a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG00558.hp1 HG01255.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+3208_472+3211d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | AATATAT | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.472+3206_472+3211d others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0125 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.472+3202_472+3211d others(12): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | AT | 5 | a0001c0001t0001g0093a0001c0001t0001g0153a0001c0001t0001g0161others(2): Show | 5 | HG00735.hp2 HG01081.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+3211_472+3212i others(3): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | ATAT | 2 | a0001c0001t0001g0090a0001c0001t0001g0157 | 2 | HG03490.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.472+3211_472+3212i others(5): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | ATATATAT | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.472+3211_472+3212i others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
A | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0017others(24): Show | 38 | HG00597.hp1 HG00735.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.472+3212T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
AAT | A | 1 | a0001c0001t0001g0010 | 3 | NA18951.hp1 NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.472+3210_472+3211d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
AATAT | A | 13 | a0001c0001t0001g0167a0001c0001t0002g0004a0001c0001t0002g0016others(10): Show | 18 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.472+3208_472+3211d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016866
|
AATATAT | A | 8 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0002g0008others(5): Show | 12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.472+3206_472+3211d others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | ||||||
chrX:14016867
|
AT | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0085a0001c0001t0001g0107others(2): Show | 5 | HG02083.hp1 HG02897.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+3210delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016867 | ||||||
chrX:14016867
|
ATAT | A | 4 | a0001c0001t0001g0028a0001c0001t0003g0053a0001c0001t0010g0183others(1): Show | 5 | HG03098.hp1 HG03516.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+3208_472+3210d others(5): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016867 | ||||||
chrX:14016867
|
ATATAT | A | 9 | a0001c0001t0002g0009a0001c0001t0002g0029a0001c0001t0002g0034others(6): Show | 16 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.472+3206_472+3210d others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016867 | ||||||
chrX:14016868
|
T | A | 12 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0063others(9): Show | 15 | HG00642.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.472+3210A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016868 | ||||||
chrX:14016872
|
T | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0167a0001c0001t0002g0043others(4): Show | 8 | HG01884.hp2 HG01993.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+3206A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016872 | ||||||
chrX:14016874
|
T | A | 11 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0002g0008others(8): Show | 15 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.472+3204A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016874 | ||||||
chrX:14016908
|
C | T | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3170G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016908 | ||||||
chrX:14016956
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.472+3122A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016956 | ||||||
chrX:14017128
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472+2950A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017128 | ||||||
chrX:14017167
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.472+2911C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017167 | ||||||
chrX:14017375
|
A | G | 46 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0002g0004others(43): Show | 67 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.472+2703T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017375 | ||||||
chrX:14017393
|
TAC | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18957.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.472+2683_472+2684d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017393 | ||||||
chrX:14017396
|
A | G | 2 | a0001c0001t0003g0053a0001c0001t0011g0054 | 2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.472+2682T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017396 | ||||||
chrX:14017483
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.472+2595C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017483 | ||||||
chrX:14017516
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472+2562G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017516 | ||||||
chrX:14017679
|
A | C | 63 | a0001c0001t0001g0028a0001c0001t0001g0078a0001c0001t0001g0079others(60): Show | 86 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.472+2399T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017679 | ||||||
chrX:14017699
|
A | G | 5 | a0001c0001t0002g0008a0001c0001t0005g0027a0001c0001t0005g0162others(2): Show | 9 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.472+2379T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017699 | ||||||
chrX:14017979
|
C | A | 1 | a0001c0001t0010g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.472+2099G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017979 | ||||||
chrX:14017987
|
T | C | 27 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0016others(24): Show | 39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.472+2091A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017987 | ||||||
chrX:14018444
|
G | C | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+1634C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018444 | ||||||
chrX:14018537
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.472+1541C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018537 | ||||||
chrX:14018574
|
G | C | 1 | a0001c0001t0008g0116 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.472+1504C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018574 | ||||||
chrX:14018766
|
C | CT | 2 | a0001c0001t0001g0087a0001c0001t0001g0194 | 2 | HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.472+1311dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018766 | ||||||
chrX:14018766
|
CT | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0085others(18): Show | 27 | HG00597.hp1 HG01069.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.472+1311delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018766 | ||||||
chrX:14018769
|
T | TG | 1 | a0001c0001t0001g0117 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.472+1308_472+1309i others(3): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018769 | ||||||
chrX:14019253
|
A | G | 45 | a0001c0001t0001g0173a0001c0001t0002g0004a0001c0001t0002g0008others(42): Show | 66 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.472+825T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019253 | ||||||
chrX:14019315
|
G | A | 3 | a0002c0002t0002g0015a0002c0002t0002g0050a0002c0002t0002g0191 | 5 | HG00597.hp1 HG02523.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+763C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019315 | ||||||
chrX:14019419
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.472+659G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019419 | ||||||
chrX:14019545
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0055 | 3 | HG00323.hp1 HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.472+533C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019545 | ||||||
chrX:14019592
|
G | A | 15 | a0001c0001t0001g0173a0002c0002t0002g0015a0002c0002t0002g0030others(12): Show | 20 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.472+486C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019592 | ||||||
chrX:14019723
|
TATATAAA others(9): Show |
T | 1 | a0001c0001t0001g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.472+339_472+354del others(16): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019723 | ||||||
chrX:14019772
|
A | G | 45 | a0001c0001t0001g0173a0001c0001t0002g0004a0001c0001t0002g0008others(42): Show | 66 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.472+306T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019772 | ||||||
chrX:14019786
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.472+292C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019786 | ||||||
chrX:14019993
|
T | C | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+85A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019993 | ||||||
chrX:14020653
|
C | CT | 48 | a0001c0001t0001g0173a0001c0001t0002g0004a0001c0001t0002g0008others(45): Show | 69 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.16-120_16-119insA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14020653 | ||||||
chrX:14020819
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0165a0001c0001t0001g0167others(2): Show | 6 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-285C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14020819 | ||||||
chrX:14021100
|
T | C | 7 | a0001c0001t0003g0026a0001c0001t0003g0053a0001c0001t0003g0074others(4): Show | 8 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+364A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021100 | ||||||
chrX:14021147
|
A | G | 1 | a0001c0001t0001g0020 | 2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.15+317T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021147 | ||||||
chrX:14021196
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0121 | 5 | HG02132.hp1 HG02523.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+268C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021196 | ||||||
chrX:14021225
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.15+239A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021225 | ||||||
chrX:14021230
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0085 | 3 | HG00438.hp1 HG02135.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.15+234G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021230 | ||||||
chrX:14021250
|
T | TG | 1 | a0001c0001t0001g0143 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.15+213dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021250 | ||||||
chrX:14021312
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.15+152C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021312 | ||||||
chrX:14021646
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33-135G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021646 | ||||||
chrX:14021759
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-33-248A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021759 | ||||||
chrX:14021806
|
A | ATG | 2 | a0001c0001t0001g0084a0002c0002t0002g0192 | 2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-33-297_-33-296dup others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021806 | ||||||
chrX:14021814
|
G | GTA | 32 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(29): Show | 48 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-33-305_-33-304dup others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTATA | 9 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0138others(6): Show | 10 | HG01070.hp2 HG02109.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33-307_-33-304dup others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTATATA | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-33-309_-33-304dup others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTATATAT others(1): Show |
2 | a0001c0001t0001g0144a0001c0001t0001g0148 | 2 | HG02630.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.-33-311_-33-304dup others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0181a0001c0001t0003g0053 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-33-313_-33-304dup others(10): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTATATAT others(5): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0145others(2): Show | 6 | HG01074.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-315_-33-304dup others(12): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTATATAT others(7): Show |
4 | a0001c0001t0001g0052a0001c0001t0001g0182a0001c0001t0003g0149others(1): Show | 4 | HG02293.hp1 HG02922.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-317_-33-304dup others(14): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0003g0026a0001c0001t0003g0151 | 3 | HG02622.hp1 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-33-319_-33-304dup others(16): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTGTATAT others(1): Show |
1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-33-304_-33-303ins others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-33-304_-33-303ins others(18): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
GTA | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0075others(2): Show | 8 | HG00558.hp2 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-305_-33-304del others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
GTATA | G | 6 | a0001c0001t0001g0080a0001c0001t0001g0165a0001c0001t0001g0167others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-307_-33-304del others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021814
|
GTATATAT others(9): Show |
G | 33 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0009others(30): Show | 49 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.-33-319_-33-304del others(16): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | ||||||
chrX:14021816
|
A | G | 14 | a0001c0001t0001g0173a0002c0002t0002g0015a0002c0002t0002g0030others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.-33-305T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021816 | ||||||
chrX:14021819
|
T | TATATATA others(38): Show |
1 | a0001c0001t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33-309_-33-308ins others(45): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021819 | ||||||
chrX:14021824
|
A | AC | 1 | a0001c0001t0001g0081 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-33-314_-33-313ins others(1): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021824 | ||||||
chrX:14021832
|
A | G | 33 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0009others(30): Show | 49 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.-33-321T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021832 | ||||||
chrX:14021913
|
TATGTATA | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0080a0001c0001t0001g0165others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-409_-33-403del others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021913 | ||||||
chrX:14021965
|
CAT | C | 8 | a0001c0001t0001g0070a0001c0001t0003g0026a0001c0001t0003g0053others(5): Show | 9 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-456_-33-455del others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021965 | ||||||
chrX:14022004
|
TATGTATG others(7): Show |
T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-33-507_-33-494del others(14): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022004 | ||||||
chrX:14022048
|
G | GTA | 15 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(12): Show | 21 | HG00140.hp1 HG01168.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.-33-539_-33-538dup others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022048 | ||||||
chrX:14022338
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-33-827A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022338 | ||||||
chrX:14022362
|
C | T | 1 | a0001c0001t0004g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-33-851G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022362 | ||||||
chrX:14022599
|
C | CT | 4 | a0001c0001t0002g0016a0001c0001t0002g0035a0001c0001t0002g0036others(1): Show | 5 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33-1089dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022599 | ||||||
chrX:14022599
|
CT | C | 15 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0172others(12): Show | 20 | HG02015.hp1 HG02145.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-33-1089delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022599 | ||||||
chrX:14023015
|
TA | T | 1 | a0001c0001t0001g0077 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-33-1505delT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023015 | ||||||
chrX:14023041
|
A | G | 2 | a0001c0001t0002g0033a0001c0001t0002g0034 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-33-1530T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023041 | ||||||
chrX:14023156
|
T | G | 1 | a0001c0001t0005g0164 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-1645A>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023156 | ||||||
chrX:14023224
|
G | A | 15 | a0001c0001t0001g0173a0002c0002t0002g0015a0002c0002t0002g0030others(12): Show | 20 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.-33-1713C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023224 | ||||||
chrX:14023381
|
C | CT | 1 | a0001c0001t0010g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33-1871_-33-1870i others(3): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023381 | ||||||
chrX:14023382
|
C | CT | 21 | a0001c0001t0001g0028a0001c0001t0001g0158a0001c0001t0001g0165others(18): Show | 27 | HG00597.hp1 HG01884.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-1872dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023382 | ||||||
chrX:14023382
|
C | T | 1 | a0001c0001t0010g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33-1871G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023382 | ||||||
chrX:14023382
|
CT | C | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0002g0029others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-1872delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023382 | ||||||
chrX:14023402
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0005g0027a0001c0001t0005g0162others(2): Show | 9 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-1891G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023402 | ||||||
chrX:14023527
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-33-2016C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023527 | ||||||
chrX:14023648
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-33-2137T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023648 | ||||||
chrX:14023672
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0165a0001c0001t0001g0167others(2): Show | 6 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-2161G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023672 | ||||||
chrX:14023747
|
G | A | 1 | a0001c0001t0005g0164 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-2236C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023747 | ||||||
chrX:14023748
|
C | CA | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-2238dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023748 | ||||||
chrX:14024261
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-34+1879C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024261 | ||||||
chrX:14024283
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0193 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-34+1857C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024283 | ||||||
chrX:14024367
|
C | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0075a0001c0001t0001g0076others(4): Show | 8 | HG00639.hp2 HG01884.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+1773G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024367 | ||||||
chrX:14024396
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0165a0001c0001t0001g0167others(2): Show | 6 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+1744C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024396 | ||||||
chrX:14024522
|
A | C | 27 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0016others(24): Show | 39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-34+1618T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024522 | ||||||
chrX:14024574
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-34+1566G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024574 | ||||||
chrX:14025023
|
T | C | 53 | a0001c0001t0001g0028a0001c0001t0001g0165a0001c0001t0001g0167others(50): Show | 75 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-34+1117A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025023 | ||||||
chrX:14025055
|
T | A | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-34+1085A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025055 | ||||||
chrX:14025260
|
T | TA | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-34+879dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025260 | ||||||
chrX:14025335
|
T | TA | 2 | a0001c0001t0001g0158a0001c0001t0003g0159 | 2 | HG02145.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-34+804dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025335 | ||||||
chrX:14025335
|
TA | T | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-34+804delT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025335 | ||||||
chrX:14025348
|
A | AC | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-34+791_-34+792ins others(1): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025348 | ||||||
chrX:14025348
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-34+792T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025348 | ||||||
chrX:14025377
|
T | TA | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-34+762dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025377 | ||||||
chrX:14025412
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-34+728G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025412 | ||||||
chrX:14025419
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-34+721A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025419 | ||||||
chrX:14025439
|
C | A | 48 | a0001c0001t0001g0173a0001c0001t0002g0004a0001c0001t0002g0008others(45): Show | 69 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.-34+701G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025439 | ||||||
chrX:14025443
|
GT | G | 1 | a0001c0001t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-34+696delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025443 | ||||||
chrX:14025475
|
A | T | 27 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0016others(24): Show | 39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-34+665T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025475 | ||||||
chrX:14026008
|
TA | T | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-34+131delT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14026008 | ||||||
chrX:14026099
|
TTGGTCTT others(3): Show |
T | 1 | a0001c0001t0001g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-34+31_-34+40delTT others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14026099 | ||||||
chrX:14026123
|
G | A | 27 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0016others(24): Show | 39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-34+17C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14026123 | ||||||
chrX:14026339
|
G | A | 33 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0009others(30): Show | 49 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.-115-118C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026339 | ||||||
chrX:14026396
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-115-175T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026396 | ||||||
chrX:14026424
|
C | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0165a0001c0001t0001g0167others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-115-203G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026424 | ||||||
chrX:14026596
|
T | TA | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-115-376dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026596 | ||||||
chrX:14026712
|
A | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(13): Show | 22 | HG00140.hp1 HG01168.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.-115-491T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026712 | ||||||
chrX:14026847
|
C | CA | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-115-627_-115-626i others(3): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026847 | ||||||
chrX:14027033
|
C | CT | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-115-813dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027033 | ||||||
chrX:14027263
|
T | C | 1 | a0002c0002t0002g0192 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-115-1042A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027263 | ||||||
chrX:14027360
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-115-1139T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027360 | ||||||
chrX:14027488
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-115-1267A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027488 | ||||||
chrX:14027809
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 13 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.-115-1588C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027809 | ||||||
chrX:14027852
|
AT | A | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-115-1632delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027852 | ||||||
chrX:14027931
|
TA | T | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-115-1711delT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027931 | ||||||
chrX:14028006
|
A | G | 1 | a0001c0001t0004g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-116+1771T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028006 | ||||||
chrX:14028116
|
CT | C | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-116+1660delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028116 | ||||||
chrX:14028156
|
TG | T | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-116+1620delC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028156 | ||||||
chrX:14028475
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-116+1302C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028475 | ||||||
chrX:14028591
|
C | CT | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-116+1185_-116+118 others(5): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028591 | ||||||
chrX:14028619
|
T | TA | 28 | a0001c0001t0001g0175a0001c0001t0002g0004a0001c0001t0002g0009others(25): Show | 40 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-116+1157dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028619 | ||||||
chrX:14028619
|
TA | T | 1 | a0001c0001t0001g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-116+1157delT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028619 | ||||||
chrX:14028628
|
A | C | 2 | a0001c0001t0003g0053a0001c0001t0011g0054 | 2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-116+1149T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028628 | ||||||
chrX:14028643
|
T | C | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02572.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-116+1134A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028643 | ||||||
chrX:14028783
|
T | C | 1 | a0001c0001t0010g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-116+994A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028783 | ||||||
chrX:14028936
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0052 | 4 | HG02293.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-116+841T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028936 | ||||||
chrX:14029112
|
G | C | 14 | a0002c0002t0002g0015a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.-116+665C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029112 | ||||||
chrX:14029152
|
C | G | 1 | a0002c0002t0002g0050 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-116+625G>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029152 | ||||||
chrX:14029242
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-116+535C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029242 | ||||||
chrX:14029334
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-116+443A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029334 | ||||||
chrX:14029715
|
G | T | 20 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0016others(17): Show | 27 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-116+62C>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029715 |