geneid | 79868 |
---|---|
ensemblid | ENSG00000101901.13 |
hgncid | 30881 |
symbol | ALG13 |
name | ALG13 UDP-N-acetylglucosaminyltransferase subunit |
refseq_nuc | NM_001099922.3 |
refseq_prot | NP_001093392.1 |
ensembl_nuc | ENST00000394780.8 |
ensembl_prot | ENSP00000378260.3 |
mane_status | MANE Select |
chr | chrX |
start | 111681170 |
end | 111760649 |
strand | + |
ver | v1.2 |
region | chrX:111681170-111760649 |
region5000 | chrX:111676170-111765649 |
regionname0 | ALG13_chrX_111681170_111760649 |
regionname5000 | ALG13_chrX_111676170_111765649 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1137 | 160 | 61 | 21 | 58 | 5 | 13 | 44 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002 | 0/0 | 1138 | 16 | 6 | 1 | 7 | 0 | 2 | 5 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0003 | 0/0 | 1136 | 5 | 4 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0004 | 0/0 | 1139 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0005 | 0/0 | 1135 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0006 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0007 | 0/0 | 947 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0008 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0009 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0010 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0011 | 0/0 | 66 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3414 | 134 | 39 | 20 | 57 | 5 | 12 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0002 | 0/0 | 3414 | 21 | 21 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0003 | 0/0 | 3417 | 11 | 2 | 1 | 7 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0004 | 0/0 | 3411 | 4 | 4 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0005 | 0/0 | 3417 | 3 | 3 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0006 | 0/1 | 3414 | 2 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0007 | 0/0 | 3414 | 2 | 0 | 0 | 1 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0008 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0009 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0010 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0011 | 0/0 | 3415 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0012 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0013 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0014 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0015 | 0/0 | 3408 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0016 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0017 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0018 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0019 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
c0020 | 0/0 | 3413 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3414 | 134 | 39 | 20 | 57 | 5 | 12 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0002 | 0/0 | 3414 | 21 | 21 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0006 | 0/1 | 3414 | 2 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0007 | 0/0 | 3414 | 2 | 0 | 0 | 1 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0017 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0003 | 0/0 | 3417 | 11 | 2 | 1 | 7 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0005 | 0/0 | 3417 | 3 | 3 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0009 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0012 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0003c0004 | 0/0 | 3411 | 4 | 4 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0003c0014 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0004c0008 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0004c0010 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0005c0015 | 0/0 | 3408 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0006c0013 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0007c0011 | 0/0 | 3415 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0008c0016 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0009c0019 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0010c0018 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0011c0020 | 0/0 | 3413 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4113 | 133 | 39 | 20 | 56 | 5 | 12 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0001t0002 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0002t0001 | 0/0 | 4113 | 21 | 21 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0006t0001 | 0/1 | 4113 | 2 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0007t0001 | 0/0 | 4113 | 2 | 0 | 0 | 1 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0001c0017t0001 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0003t0001 | 0/0 | 4116 | 11 | 2 | 1 | 7 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0005t0001 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0009t0001 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0002c0012t0001 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0003c0004t0001 | 0/0 | 4110 | 4 | 4 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0003c0014t0001 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0004c0008t0001 | 0/0 | 4119 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0004c0010t0001 | 0/0 | 4119 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0005c0015t0001 | 0/0 | 4107 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0006c0013t0001 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0007c0011t0001 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0008c0016t0001 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0009c0019t0001 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0010c0018t0001 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
a0011c0020t0001 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | copy fasta | chrX | 111676170 | 111765649 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0006t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0006t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0001c0017t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0005t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0009t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0002c0012t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0003c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0003c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0003c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0003c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0003c0014t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0004c0008t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0004c0008t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0004c0010t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0005c0015t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0006c0013t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0007c0011t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0008c0016t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0009c0019t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0010c0018t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
a0011c0020t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | FIN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00558 | hp1 | a0003 | c0014 | t0001 | g0095 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00558 | hp2 | a0001 | c0007 | t0001 | g0101 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01099 | hp1 | a0002 | c0003 | t0001 | g0080 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01358 | hp1 | a0001 | c0006 | t0001 | g0153 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01496 | hp2 | a0008 | c0016 | t0001 | g0106 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0176 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02257 | hp1 | a0002 | c0005 | t0001 | g0077 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02258 | hp1 | a0004 | c0010 | t0001 | g0046 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02602 | hp1 | a0001 | c0007 | t0001 | g0130 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02698 | hp1 | a0002 | c0012 | t0001 | g0084 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02738 | hp1 | a0005 | c0015 | t0001 | g0156 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02897 | hp2 | a0001 | c0017 | t0001 | g0042 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02965 | hp1 | a0003 | c0004 | t0001 | g0067 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02976 | hp1 | a0003 | c0004 | t0001 | g0010 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02976 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03139 | hp1 | a0002 | c0009 | t0001 | g0047 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0065 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0068 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03579 | hp1 | a0002 | c0005 | t0001 | g0026 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0181 | SAS | BEB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18967 | hp1 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18995 | hp1 | a0006 | c0013 | t0001 | g0163 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19006 | hp1 | a0007 | c0011 | t0001 | g0155 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0050 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19058 | hp1 | a0011 | c0020 | t0001 | g0006 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19063 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0148 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19068 | hp1 | a0009 | c0019 | t0001 | g0132 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19086 | hp1 | a0010 | c0018 | t0001 | g0145 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ASW | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG03471 | hp1 | a0003 | c0004 | t0001 | g0069 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
HG06807 | hp2 | a0004 | c0008 | t0001 | g0017 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA20300 | hp1 | a0004 | c0008 | t0001 | g0018 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
homoSapiens_chm13v2 | hp1 | a0001 | c0006 | t0001 | g0179 | REF | REF | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0093 | REF | REF | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
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:111682131
|
GA | G | 1 | a0011 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.85delA | p.Ile29fs | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/27 | 134/4113 | 85/3414 | 29/1137 | INFO_REALIGN_3_PRIME | chrX | 111682131 | |
chrX:111711720
|
C | T | 1 | a0010 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.880C>T | p.Pro294Ser | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 6/27 | 929/4113 | 880/3414 | 294/1137 | chrX | 111711720 | ||
chrX:111712521
|
T | C | 1 | a0009 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.923T>C | p.Leu308Pro | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 7/27 | 972/4113 | 923/3414 | 308/1137 | chrX | 111712521 | ||
chrX:111721664
|
A | G | 1 | a0008 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1388A>G | p.Glu463Gly | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 12/27 | 1437/4113 | 1388/3414 | 463/1137 | chrX | 111721664 | ||
chrX:111744725
|
T | TACC | 2 | a0001a0002 | 16 | HG00558.hp2 HG01099.hp1 HG02027.hp1 others(13): Show |
disruptive_inframe_insertion | MODERATE | c.2796_2798dupACC | p.Pro933dup | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2848/4113 | 2799/3414 | 933/1137 | INFO_REALIGN_3_PRIME | chrX | 111744725 | |
chrX:111744725
|
T | TACCACC | 1 | a0004 | 3 | HG02258.hp1 HG06807.hp2 NA20300.hp1 |
disruptive_inframe_insertion | MODERATE | c.2793_2798dupACCACC | p.Pro932_Pro933dup | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2848/4113 | 2799/3414 | 933/1137 | INFO_REALIGN_3_PRIME | chrX | 111744725 | |
chrX:111744725
|
TACC | T | 1 | a0003 | 1 | HG00558.hp1 | disruptive_inframe_deletion | MODERATE | c.2796_2798delACC | p.Pro933del | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2845/4113 | 2796/3414 | 932/1137 | INFO_REALIGN_3_PRIME | chrX | 111744725 | |
chrX:111744725
|
TACCACC | T | 1 | a0005 | 1 | HG02738.hp1 | disruptive_inframe_deletion | MODERATE | c.2793_2798delACCACC | p.Pro932_Pro933del | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2842/4113 | 2793/3414 | 931/1137 | INFO_REALIGN_3_PRIME | chrX | 111744725 | |
chrX:111744768
|
A | AC | 1 | a0007 | 1 | NA19006.hp1 | frameshift_variant | HIGH | c.2798dupC | p.Pro934fs | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2848/4113 | 2799/3414 | 933/1137 | INFO_REALIGN_3_PRIME | chrX | 111744768 | |
chrX:111744768
|
A | ACCT | 1 | a0002 | 1 | HG02698.hp1 | conservative_inframe_insertion | MODERATE | c.2833_2835dupCCT | p.Pro945dup | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2885/4113 | 2836/3414 | 946/1137 | INFO_REALIGN_3_PRIME | chrX | 111744768 | |
chrX:111744768
|
ACCT | A | 2 | a0001a0003 | 5 | HG00558.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
conservative_inframe_deletion | MODERATE | c.2833_2835delCCT | p.Pro945del | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2882/4113 | 2833/3414 | 945/1137 | INFO_REALIGN_3_PRIME | chrX | 111744768 | |
chrX:111744806
|
C | T | 1 | a0006 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.2834C>T | p.Pro945Leu | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2883/4113 | 2834/3414 | 945/1137 | chrX | 111744806 |
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:111685054
|
C | T | 1 | a0009c0019 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.334C>T | p.Leu112Leu | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/27 | 383/4113 | 334/3414 | 112/1137 | chrX | 111685054 | ||
chrX:111718176
|
G | A | 1 | a0002c0009 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1152G>A | p.Ala384Ala | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/27 | 1201/4113 | 1152/3414 | 384/1137 | chrX | 111718176 | ||
chrX:111720110
|
T | C | 1 | a0001c0006 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.1266T>C | p.Gly422Gly | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/27 | 1315/4113 | 1266/3414 | 422/1137 | chrX | 111720110 | ||
chrX:111720137
|
A | G | 5 | a0001c0002a0001c0017a0002c0005others(2): Show | 28 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
synonymous_variant | LOW | c.1293A>G | p.Pro431Pro | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/27 | 1342/4113 | 1293/3414 | 431/1137 | chrX | 111720137 | ||
chrX:111744771
|
T | A | 1 | a0001c0007 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.2799T>A | p.Pro933Pro | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2848/4113 | 2799/3414 | 933/1137 | chrX | 111744771 | ||
chrX:111757653
|
A | G | 1 | a0001c0017 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.3039A>G | p.Val1013Val | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/27 | 3088/4113 | 3039/3414 | 1013/1137 | chrX | 111757653 |
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:111760578
|
C | T | 1 | a0001c0001t0002 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 27/27 | 579 | chrX | 111760578 |
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:111681395
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.81+96C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681395 | ||||||
chrX:111681512
|
TC | T | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.81+216delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681512 | |||||
chrX:111681562
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.81+263G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681562 | ||||||
chrX:111681572
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81+273G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681572 | ||||||
chrX:111681595
|
T | TCCTCCGC others(1): Show |
1 | a0001c0001t0001g0009 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.81+302_81+309dupGC others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681595 | |||||
chrX:111681630
|
G | A | 1 | a0003c0004t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.81+331G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681630 | ||||||
chrX:111681644
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+345C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681644 | ||||||
chrX:111681757
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01934.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.82-375G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681757 | ||||||
chrX:111681852
|
GT | G | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.82-278delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681852 | |||||
chrX:111681872
|
TC | T | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.82-258delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681872 | |||||
chrX:111681890
|
TC | T | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.82-240delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681890 | |||||
chrX:111681928
|
G | GC | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.82-203dupC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681928 | |||||
chrX:111681980
|
A | ATACTT | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.82-150_82-149insCT others(3): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681980 | |||||
chrX:111682072
|
TC | T | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.82-58delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111682072 | |||||
chrX:111682362
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.244+68C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111682362 | ||||||
chrX:111682469
|
T | TC | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.244+178dupC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111682469 | |||||
chrX:111682860
|
C | CA | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.244+567dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111682860 | |||||
chrX:111682900
|
GC | G | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.244+609delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111682900 | |||||
chrX:111682980
|
G | GA | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.244+688dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111682980 | |||||
chrX:111682994
|
C | T | 1 | a0002c0005t0001g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.244+700C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111682994 | ||||||
chrX:111683007
|
CT | C | 1 | a0001c0001t0001g0079 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.244+725delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683007 | |||||
chrX:111683010
|
T | TA | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.244+716_244+717ins others(1): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683010 | ||||||
chrX:111683156
|
T | TG | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.244+862_244+863ins others(1): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683156 | ||||||
chrX:111683289
|
GT | G | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.244+997delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683289 | |||||
chrX:111683326
|
A | AT | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(11): Show | 14 | HG02257.hp2 HG02818.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+1051dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683326 | |||||
chrX:111683326
|
A | ATT | 1 | a0001c0001t0001g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.244+1050_244+1051d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683326 | |||||
chrX:111683326
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244+1032A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683326 | ||||||
chrX:111683326
|
AT | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+1051delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683326 | |||||
chrX:111683394
|
A | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+1100A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683394 | ||||||
chrX:111683398
|
C | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0058a0001c0002t0001g0059others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+1104C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683398 | ||||||
chrX:111683497
|
AT | A | 1 | a0002c0003t0001g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.244+1213delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683497 | |||||
chrX:111683856
|
G | A | 3 | a0001c0002t0001g0019a0004c0008t0001g0017a0004c0008t0001g0018 | 3 | HG01891.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.245-1109G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683856 | ||||||
chrX:111684039
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.245-926C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111684039 | ||||||
chrX:111684096
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 5 | NA18943.hp1 NA18959.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-869G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111684096 | ||||||
chrX:111684318
|
C | CT | 1 | a0011c0020t0001g0006 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.245-637dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111684318 | |||||
chrX:111685341
|
G | GT | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.383+239dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111685341 | |||||
chrX:111685364
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383+261G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111685364 | ||||||
chrX:111685846
|
C | T | 1 | a0001c0006t0001g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.383+743C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111685846 | ||||||
chrX:111685923
|
A | G | 1 | a0002c0005t0001g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.383+820A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111685923 | ||||||
chrX:111685934
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(19): Show | 23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.383+831G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111685934 | ||||||
chrX:111686132
|
A | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.383+1029A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686132 | ||||||
chrX:111686164
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.383+1061C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686164 | ||||||
chrX:111686232
|
G | A | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+1129G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686232 | ||||||
chrX:111686689
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.383+1586A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686689 | ||||||
chrX:111686727
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.383+1624A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686727 | ||||||
chrX:111686822
|
G | A | 1 | a0001c0006t0001g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.383+1719G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686822 | ||||||
chrX:111686831
|
A | T | 1 | a0002c0003t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.383+1728A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686831 | ||||||
chrX:111687023
|
T | C | 1 | a0001c0002t0001g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.383+1920T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687023 | ||||||
chrX:111687102
|
G | A | 26 | a0001c0001t0001g0036a0001c0002t0001g0001a0001c0002t0001g0019others(23): Show | 27 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.383+1999G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687102 | ||||||
chrX:111687209
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(7): Show | 10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.383+2106T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687209 | ||||||
chrX:111687309
|
A | G | 1 | a0002c0003t0001g0176 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.383+2206A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687309 | ||||||
chrX:111687612
|
T | C | 1 | a0002c0012t0001g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.383+2509T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687612 | ||||||
chrX:111687763
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383+2660T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687763 | ||||||
chrX:111687766
|
CAT | C | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.383+2664_383+2665d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687766 | ||||||
chrX:111688035
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.383+2932C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688035 | ||||||
chrX:111688374
|
TA | T | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.383+3278delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111688374 | |||||
chrX:111688420
|
A | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.383+3317A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688420 | ||||||
chrX:111688566
|
CT | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+3472delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111688566 | |||||
chrX:111688580
|
A | AACAT | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.383+3481_383+3484d others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111688580 | |||||
chrX:111688632
|
G | A | 2 | a0004c0008t0001g0017a0004c0008t0001g0018 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.383+3529G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688632 | ||||||
chrX:111688684
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+3581A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688684 | ||||||
chrX:111688862
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.383+3759A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688862 | ||||||
chrX:111688988
|
A | G | 23 | a0001c0001t0001g0036a0001c0002t0001g0001a0001c0002t0001g0019others(20): Show | 24 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+3885A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688988 | ||||||
chrX:111689114
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.383+4011G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689114 | ||||||
chrX:111689303
|
T | G | 3 | a0001c0002t0001g0019a0004c0008t0001g0017a0004c0008t0001g0018 | 3 | HG01891.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.383+4200T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689303 | ||||||
chrX:111689315
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383+4212C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689315 | ||||||
chrX:111689561
|
G | C | 23 | a0001c0001t0001g0036a0001c0002t0001g0001a0001c0002t0001g0019others(20): Show | 24 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+4458G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689561 | ||||||
chrX:111689926
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG01884.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.383+4823G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689926 | ||||||
chrX:111690333
|
G | A | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+5230G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690333 | ||||||
chrX:111690344
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.383+5241C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690344 | ||||||
chrX:111690453
|
T | G | 1 | a0001c0001t0001g0086 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.383+5350T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690453 | ||||||
chrX:111690613
|
A | AT | 1 | a0001c0017t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.383+5523dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111690613 | |||||
chrX:111690631
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.383+5528T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690631 | ||||||
chrX:111690646
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.383+5543G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690646 | ||||||
chrX:111690798
|
G | GAC | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.383+5696_383+5697i others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111690798 | |||||
chrX:111691000
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0003t0001g0090others(1): Show | 4 | HG02027.hp1 NA18967.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+5897G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691000 | ||||||
chrX:111691027
|
C | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.383+5924C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691027 | ||||||
chrX:111691048
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG01884.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.383+5945A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691048 | ||||||
chrX:111691376
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.383+6273C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691376 | ||||||
chrX:111691739
|
G | GGTATGCT others(1): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG02451.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.383+6638_383+6645d others(10): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111691739 | |||||
chrX:111691859
|
G | A | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+6756G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691859 | ||||||
chrX:111691894
|
C | A | 1 | a0001c0002t0001g0022 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383+6791C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691894 | ||||||
chrX:111691905
|
G | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.383+6802G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691905 | ||||||
chrX:111692031
|
A | G | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+6928A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111692031 | ||||||
chrX:111692801
|
A | AT | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+7708dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111692801 | |||||
chrX:111692822
|
A | AG | 1 | a0001c0001t0001g0088 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.383+7722dupG | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111692822 | |||||
chrX:111692863
|
A | C | 28 | a0001c0001t0001g0036a0001c0002t0001g0001a0001c0002t0001g0019others(25): Show | 29 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.383+7760A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111692863 | ||||||
chrX:111693130
|
C | T | 25 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0020others(22): Show | 26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.383+8027C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693130 | ||||||
chrX:111693164
|
C | CT | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | NA18955.hp1 NA18977.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+8083dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111693164 | |||||
chrX:111693164
|
CT | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0096others(3): Show | 6 | HG00558.hp1 HG00642.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+8083delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111693164 | |||||
chrX:111693164
|
CTT | C | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.383+8082_383+8083d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111693164 | |||||
chrX:111693260
|
A | AT | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+8171dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111693260 | |||||
chrX:111693260
|
A | ATT | 1 | a0001c0001t0001g0175 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.383+8170_383+8171d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111693260 | |||||
chrX:111693263
|
T | TA | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+8160_383+8161i others(3): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693263 | ||||||
chrX:111693264
|
T | A | 25 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0020others(22): Show | 26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.383+8161T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693264 | ||||||
chrX:111693387
|
A | C | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+8284A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693387 | ||||||
chrX:111693429
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0086others(8): Show | 12 | NA18952.hp1 NA18965.hp1 NA18966.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+8326A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693429 | ||||||
chrX:111693899
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(19): Show | 23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.383+8796G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693899 | ||||||
chrX:111694051
|
A | AT | 23 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0037others(20): Show | 24 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+8958dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694051 | |||||
chrX:111694055
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.383+8952T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111694055 | ||||||
chrX:111694075
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.383+8972G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111694075 | ||||||
chrX:111694135
|
TC | T | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9033delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111694135 | ||||||
chrX:111694148
|
A | AT | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9047dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694148 | |||||
chrX:111694340
|
C | CG | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9239dupG | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694340 | |||||
chrX:111694530
|
A | G | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.383+9427A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111694530 | ||||||
chrX:111694640
|
A | AC | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9540dupC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694640 | |||||
chrX:111694712
|
T | TTA | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9610_383+9611i others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694712 | |||||
chrX:111694719
|
C | CA | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9617dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694719 | |||||
chrX:111694727
|
C | CA | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9625dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694727 | |||||
chrX:111694762
|
AG | A | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9663delG | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694762 | |||||
chrX:111694961
|
G | GT | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9860dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694961 | |||||
chrX:111695006
|
T | C | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+9903T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695006 | ||||||
chrX:111695078
|
GT | G | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+9978delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111695078 | |||||
chrX:111695164
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.383+10061G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695164 | ||||||
chrX:111695251
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+10148C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695251 | ||||||
chrX:111695433
|
T | G | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(71): Show | 75 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(72): Show |
intron_variant | MODIFIER | c.383+10330T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695433 | ||||||
chrX:111695517
|
CTG | C | 1 | a0002c0003t0001g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.383+10416_383+1041 others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111695517 | |||||
chrX:111695522
|
T | TA | 2 | a0001c0001t0001g0009a0001c0001t0001g0100 | 2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.383+10435dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111695522 | |||||
chrX:111695522
|
TA | T | 1 | a0001c0001t0001g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.383+10435delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111695522 | |||||
chrX:111695535
|
A | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG01069.hp1 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.383+10432A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695535 | ||||||
chrX:111695555
|
G | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.383+10452G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695555 | ||||||
chrX:111695695
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | NA18990.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.383+10592C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695695 | ||||||
chrX:111695961
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(19): Show | 23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.383+10858G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695961 | ||||||
chrX:111696068
|
G | T | 1 | a0001c0002t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383+10965G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696068 | ||||||
chrX:111696149
|
A | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+11046A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696149 | ||||||
chrX:111696176
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.383+11073A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696176 | ||||||
chrX:111696582
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.384-11445G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696582 | ||||||
chrX:111696587
|
G | A | 1 | a0001c0007t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.384-11440G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696587 | ||||||
chrX:111696916
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.384-11111G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696916 | ||||||
chrX:111696982
|
C | CT | 36 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0036others(33): Show | 36 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.384-11024dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111696982 | |||||
chrX:111696982
|
C | CTT | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0074 | 3 | HG01106.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.384-11025_384-1102 others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111696982 | |||||
chrX:111696982
|
CT | C | 29 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(26): Show | 30 | HG01167.hp1 HG01256.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.384-11024delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111696982 | |||||
chrX:111696982
|
CTT | C | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.384-11025_384-1102 others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111696982 | |||||
chrX:111696982
|
CTTT | C | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.384-11026_384-1102 others(7): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111696982 | |||||
chrX:111697929
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.384-10098A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111697929 | ||||||
chrX:111698040
|
A | AT | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.384-9985dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111698040 | |||||
chrX:111698499
|
C | T | 2 | a0001c0001t0001g0105a0008c0016t0001g0106 | 2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.384-9528C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698499 | ||||||
chrX:111698627
|
C | G | 1 | a0001c0006t0001g0153 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.384-9400C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698627 | ||||||
chrX:111698682
|
A | G | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-9345A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698682 | ||||||
chrX:111698695
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-9332G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698695 | ||||||
chrX:111698914
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-9113A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698914 | ||||||
chrX:111699047
|
A | G | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.384-8980A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699047 | ||||||
chrX:111699187
|
T | C | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(69): Show | 73 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.384-8840T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699187 | ||||||
chrX:111699242
|
G | GT | 1 | a0005c0015t0001g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.384-8775dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111699242 | |||||
chrX:111699894
|
A | AT | 3 | a0001c0017t0001g0042a0002c0003t0001g0091a0005c0015t0001g0156 | 3 | HG02738.hp1 HG02897.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.384-8122dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111699894 | |||||
chrX:111699894
|
AT | A | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-8122delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111699894 | |||||
chrX:111699905
|
TC | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0058a0001c0002t0001g0059others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-8121delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699905 | ||||||
chrX:111699906
|
C | T | 18 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.384-8121C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699906 | ||||||
chrX:111700038
|
G | GT | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(41): Show | 44 | HG00621.hp1 HG01099.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.384-7973dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700038 | |||||
chrX:111700038
|
G | GTT | 3 | a0001c0001t0001g0152a0001c0002t0001g0035a0004c0010t0001g0046 | 3 | HG02258.hp1 HG03486.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.384-7974_384-7973d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700038 | |||||
chrX:111700038
|
G | GTTT | 1 | a0001c0001t0001g0180 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.384-7975_384-7973d others(5): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700038 | |||||
chrX:111700038
|
GT | G | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0107others(7): Show | 10 | HG01074.hp1 HG01106.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.384-7973delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700038 | |||||
chrX:111700191
|
G | A | 27 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0020others(24): Show | 28 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.384-7836G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700191 | ||||||
chrX:111700202
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.384-7825A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700202 | ||||||
chrX:111700494
|
CT | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-7532delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700494 | ||||||
chrX:111700575
|
G | GT | 1 | a0001c0001t0001g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.384-7443dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700575 | |||||
chrX:111700585
|
G | GT | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.384-7433dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700585 | |||||
chrX:111700677
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0174 | 2 | HG02083.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.384-7350A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700677 | ||||||
chrX:111700751
|
A | AT | 34 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0001g0053others(31): Show | 35 | HG01106.hp1 HG01891.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.384-7255dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700751 | |||||
chrX:111700751
|
A | ATT | 6 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.384-7256_384-7255d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700751 | |||||
chrX:111700751
|
AT | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0166a0001c0001t0001g0183 | 3 | HG03516.hp1 NA18984.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.384-7255delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700751 | |||||
chrX:111701557
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.384-6470C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111701557 | ||||||
chrX:111701895
|
T | A | 1 | a0001c0002t0001g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.384-6132T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111701895 | ||||||
chrX:111701902
|
CT | C | 1 | a0007c0011t0001g0155 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.384-6120delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111701902 | |||||
chrX:111702224
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.384-5803T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702224 | ||||||
chrX:111702660
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.384-5367A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702660 | ||||||
chrX:111702731
|
A | G | 11 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0049others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.384-5296A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702731 | ||||||
chrX:111702780
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-5247T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702780 | ||||||
chrX:111702827
|
C | A | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.384-5200C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702827 | ||||||
chrX:111702841
|
C | CT | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-5175dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111702841 | |||||
chrX:111703152
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-4875T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111703152 | ||||||
chrX:111703185
|
G | GTCA | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(7): Show | 10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.384-4813_384-4811d others(5): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111703185 | |||||
chrX:111703185
|
GTCATCA | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-4816_384-4811d others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111703185 | |||||
chrX:111703472
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.384-4555C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111703472 | ||||||
chrX:111703758
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0058a0001c0002t0001g0059others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-4269A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111703758 | ||||||
chrX:111704381
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.384-3646T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704381 | ||||||
chrX:111704399
|
T | C | 1 | a0001c0002t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.384-3628T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704399 | ||||||
chrX:111704557
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.384-3470T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704557 | ||||||
chrX:111704883
|
T | G | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.384-3144T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704883 | ||||||
chrX:111704954
|
A | G | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.384-3073A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704954 | ||||||
chrX:111705181
|
A | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-2846A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705181 | ||||||
chrX:111705420
|
C | CT | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-2606dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111705420 | |||||
chrX:111705563
|
G | C | 1 | a0002c0003t0001g0176 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.384-2464G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705563 | ||||||
chrX:111705632
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.384-2395T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705632 | ||||||
chrX:111705642
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.384-2385A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705642 | ||||||
chrX:111706059
|
C | CT | 12 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(9): Show | 12 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.384-1955dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111706059 | |||||
chrX:111706140
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.384-1887C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111706140 | ||||||
chrX:111706923
|
C | CA | 2 | a0001c0001t0001g0113a0002c0005t0001g0077 | 2 | HG02257.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.384-1088dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111706923 | |||||
chrX:111706923
|
CA | C | 2 | a0001c0001t0001g0167a0001c0017t0001g0042 | 2 | HG02897.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.384-1088delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111706923 | |||||
chrX:111707378
|
G | A | 4 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0033others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-649G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707378 | ||||||
chrX:111707428
|
T | C | 1 | a0001c0017t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.384-599T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707428 | ||||||
chrX:111707814
|
C | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.384-213C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707814 | ||||||
chrX:111707883
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.384-144C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707883 | ||||||
chrX:111708780
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.751-185A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 4/26 | chrX | 111708780 | ||||||
chrX:111709163
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG02257.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+115T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111709163 | ||||||
chrX:111709242
|
A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+194A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111709242 | ||||||
chrX:111709685
|
C | CT | 26 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0001g0110others(23): Show | 27 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.834+651dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chrX | 111709685 | |||||
chrX:111709814
|
A | G | 1 | a0002c0003t0001g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.834+766A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111709814 | ||||||
chrX:111710027
|
C | CT | 1 | a0002c0003t0001g0091 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.834+992dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chrX | 111710027 | |||||
chrX:111710027
|
C | CTT | 1 | a0001c0001t0001g0097 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.834+991_834+992dup others(2): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chrX | 111710027 | |||||
chrX:111710027
|
CT | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(18): Show | 21 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.834+992delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chrX | 111710027 | |||||
chrX:111710122
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.834+1074G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710122 | ||||||
chrX:111710179
|
C | T | 1 | a0002c0005t0001g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.834+1131C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710179 | ||||||
chrX:111710189
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.834+1141C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710189 | ||||||
chrX:111710301
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | NA18966.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.834+1253G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710301 | ||||||
chrX:111710727
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.835-948T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710727 | ||||||
chrX:111710904
|
C | T | 1 | a0004c0010t0001g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.835-771C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710904 | ||||||
chrX:111710918
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.835-757C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710918 | ||||||
chrX:111710977
|
G | A | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(5): Show | 8 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-698G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710977 | ||||||
chrX:111711307
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-368C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711307 | ||||||
chrX:111711403
|
A | G | 1 | a0001c0007t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.835-272A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711403 | ||||||
chrX:111711411
|
T | G | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.835-264T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711411 | ||||||
chrX:111711653
|
T | C | 59 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(56): Show | 60 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.835-22T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711653 | ||||||
chrX:111712880
|
T | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.933-345T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 7/26 | chrX | 111712880 | ||||||
chrX:111713016
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.933-209A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 7/26 | chrX | 111713016 | ||||||
chrX:111713738
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1005+441C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111713738 | ||||||
chrX:111713892
|
G | A | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1005+595G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111713892 | ||||||
chrX:111713899
|
G | C | 2 | a0001c0001t0001g0105a0008c0016t0001g0106 | 2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1005+602G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111713899 | ||||||
chrX:111714032
|
G | T | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+735G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714032 | ||||||
chrX:111714033
|
A | T | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+736A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714033 | ||||||
chrX:111714049
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1005+752G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714049 | ||||||
chrX:111714680
|
A | C | 1 | a0001c0002t0001g0019 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1005+1383A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714680 | ||||||
chrX:111714898
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1005+1601T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714898 | ||||||
chrX:111715602
|
C | T | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1006-2244C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715602 | ||||||
chrX:111715649
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1006-2197C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715649 | ||||||
chrX:111715696
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1006-2150C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715696 | ||||||
chrX:111715753
|
A | C | 1 | a0002c0003t0001g0090 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1006-2093A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715753 | ||||||
chrX:111716076
|
A | G | 2 | a0004c0008t0001g0017a0004c0008t0001g0018 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1006-1770A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111716076 | ||||||
chrX:111716154
|
C | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1006-1692C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111716154 | ||||||
chrX:111716597
|
TAACTTA | T | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-1243_1006-123 others(10): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111716597 | |||||
chrX:111716672
|
A | G | 17 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(14): Show | 18 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1006-1174A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111716672 | ||||||
chrX:111716929
|
A | AT | 2 | a0001c0001t0001g0053a0002c0003t0001g0181 | 2 | HG02630.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1006-908dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111716929 | |||||
chrX:111717361
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1006-485C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717361 | ||||||
chrX:111717541
|
C | CT | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 17 | HG00642.hp1 HG00673.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-286dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111717541 | |||||
chrX:111717541
|
C | CTT | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1006-287_1006-286d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111717541 | |||||
chrX:111717541
|
C | CTTT | 1 | a0002c0003t0001g0091 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1006-288_1006-286d others(5): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111717541 | |||||
chrX:111717541
|
CT | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0002t0001g0021 | 3 | HG02615.hp2 HG02735.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1006-286delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111717541 | |||||
chrX:111717679
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1006-167G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717679 | ||||||
chrX:111717726
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1006-120A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717726 | ||||||
chrX:111717732
|
T | C | 1 | a0007c0011t0001g0155 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1006-114T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717732 | ||||||
chrX:111717749
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-97A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717749 | ||||||
chrX:111718057
|
A | G | 1 | a0001c0017t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1088-55A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 9/26 | chrX | 111718057 | ||||||
chrX:111718385
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250+111C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718385 | ||||||
chrX:111718425
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1250+151A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718425 | ||||||
chrX:111718590
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1250+316C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718590 | ||||||
chrX:111718623
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0003t0001g0090others(1): Show | 4 | HG02027.hp1 NA18967.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+349G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718623 | ||||||
chrX:111719025
|
C | CT | 16 | a0001c0001t0001g0009a0001c0001t0001g0100a0001c0001t0001g0111others(13): Show | 16 | HG00609.hp1 HG00673.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1250+770dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chrX | 111719025 | |||||
chrX:111719025
|
C | CTT | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA19076.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1250+769_1250+770d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chrX | 111719025 | |||||
chrX:111719025
|
CT | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(44): Show | 47 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1250+770delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chrX | 111719025 | |||||
chrX:111719025
|
CTT | C | 25 | a0001c0001t0001g0038a0001c0002t0001g0001a0001c0002t0001g0019others(22): Show | 26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1250+769_1250+770d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chrX | 111719025 | |||||
chrX:111719657
|
G | A | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(66): Show | 70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.1251-438G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111719657 | ||||||
chrX:111720008
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1251-87C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111720008 | ||||||
chrX:111720217
|
G | A | 1 | a0001c0002t0001g0022 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1326+47G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | chrX | 111720217 | ||||||
chrX:111720824
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1326+654G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | chrX | 111720824 | ||||||
chrX:111720919
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1327-684G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | chrX | 111720919 | ||||||
chrX:111721056
|
G | GT | 5 | a0001c0001t0001g0104a0001c0001t0001g0136a0001c0001t0001g0174others(2): Show | 5 | HG01256.hp1 NA19005.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-533dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721056 | |||||
chrX:111721056
|
GT | G | 3 | a0001c0001t0001g0114a0002c0003t0001g0148a0011c0020t0001g0006 | 3 | NA18953.hp1 NA19058.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1327-533delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721056 | |||||
chrX:111721071
|
A | AAGAAGGA others(25): Show |
28 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0085others(25): Show | 29 | HG01261.hp1 HG01433.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1327-73_1327-42dup others(32): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(57): Show |
31 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(28): Show | 32 | HG00621.hp1 HG01167.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1327-105_1327-42du others(65): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(89): Show |
26 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0038others(23): Show | 26 | HG01069.hp1 HG01099.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.1327-137_1327-42du others(97): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(121): Show |
9 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0071others(6): Show | 9 | HG01255.hp1 HG01928.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327-169_1327-42du others(129): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(153): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0036others(4): Show | 8 | HG00609.hp1 HG02622.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1327-201_1327-42du others(161): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(185): Show |
5 | a0001c0001t0001g0037a0001c0001t0001g0061a0001c0001t0001g0070others(2): Show | 5 | HG01243.hp1 HG02897.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-233_1327-42du others(193): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(217): Show |
9 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(6): Show | 9 | HG00673.hp1 HG01106.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327-265_1327-42du others(225): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(249): Show |
8 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0057others(5): Show | 8 | HG01109.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1327-297_1327-42du others(257): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(281): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0078 | 2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1327-329_1327-42du others(289): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(313): Show |
7 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0052others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1327-361_1327-42du others(321): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(345): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0002t0001g0020others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327-393_1327-42du others(353): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(377): Show |
3 | a0001c0001t0001g0016a0001c0002t0001g0021a0004c0008t0001g0018 | 3 | HG02615.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1327-425_1327-42du others(385): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(409): Show |
5 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1327-457_1327-42du others(417): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(441): Show |
4 | a0001c0002t0001g0001a0001c0002t0001g0058a0001c0002t0001g0059others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-489_1327-42du others(449): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(473): Show |
2 | a0001c0002t0001g0019a0002c0005t0001g0023 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1327-521_1327-42du others(481): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(505): Show |
3 | a0001c0002t0001g0033a0001c0002t0001g0060a0002c0005t0001g0026 | 3 | HG02486.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1327-42_1327-41ins others(512): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(537): Show |
1 | a0001c0002t0001g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1327-42_1327-41ins others(544): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
A | AAGAAGGA others(569): Show |
1 | a0001c0002t0001g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1327-42_1327-41ins others(576): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
AAGAAGGA others(25): Show |
A | 6 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0139others(3): Show | 6 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1327-73_1327-42del others(32): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
AAGAAGGA others(57): Show |
A | 2 | a0001c0001t0001g0157a0001c0001t0001g0173 | 2 | HG00280.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1327-105_1327-42de others(65): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721071
|
AAGAAGGA others(89): Show |
A | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1327-137_1327-42de others(97): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | |||||
chrX:111721716
|
A | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
splice_region_variant&intron_variant | LOW | c.1435+5A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 12/26 | chrX | 111721716 | ||||||
chrX:111721754
|
CAGG | C | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1435+46_1435+48del others(3): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chrX | 111721754 | |||||
chrX:111722341
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1436-452G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 12/26 | chrX | 111722341 | ||||||
chrX:111723112
|
T | G | 1 | a0002c0005t0001g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1500+255T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723112 | ||||||
chrX:111723153
|
A | T | 1 | a0001c0001t0001g0103 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1500+296A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723153 | ||||||
chrX:111723415
|
G | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1501-383G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723415 | ||||||
chrX:111723500
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG02451.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1501-298G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723500 | ||||||
chrX:111723595
|
CTG | C | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1501-199_1501-198d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chrX | 111723595 | |||||
chrX:111724032
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1601+134T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 14/26 | chrX | 111724032 | ||||||
chrX:111724740
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1602-194C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 14/26 | chrX | 111724740 | ||||||
chrX:111724743
|
TA | T | 1 | a0001c0001t0001g0147 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1602-190delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 14/26 | chrX | 111724743 | ||||||
chrX:111725122
|
G | A | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(66): Show | 70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.1729+61G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111725122 | ||||||
chrX:111725199
|
T | C | 1 | a0003c0014t0001g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1729+138T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111725199 | ||||||
chrX:111725603
|
G | T | 1 | a0001c0002t0001g0019 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1729+542G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111725603 | ||||||
chrX:111726007
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1730-802T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726007 | ||||||
chrX:111726045
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730-764G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726045 | ||||||
chrX:111726132
|
A | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1730-677A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726132 | ||||||
chrX:111726232
|
G | GT | 29 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0072others(26): Show | 29 | HG00642.hp1 HG01192.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1730-556dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chrX | 111726232 | |||||
chrX:111726232
|
G | GTT | 9 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0001g0074others(6): Show | 9 | HG02056.hp1 HG02257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1730-557_1730-556d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chrX | 111726232 | |||||
chrX:111726232
|
G | GTTT | 1 | a0003c0004t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1730-558_1730-556d others(5): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chrX | 111726232 | |||||
chrX:111726232
|
GT | G | 39 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00558.hp2 HG01106.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1730-556delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chrX | 111726232 | |||||
chrX:111726415
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1730-394G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726415 | ||||||
chrX:111726422
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | NA18990.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1730-387C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726422 | ||||||
chrX:111726424
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(19): Show | 23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1730-385G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726424 | ||||||
chrX:111728143
|
A | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2248-42A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 18/26 | chrX | 111728143 | ||||||
chrX:111728181
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | splice_region_variant&intron_variant | LOW | c.2248-4A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 18/26 | chrX | 111728181 | ||||||
chrX:111728706
|
C | T | 25 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0020others(22): Show | 26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2368+401C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111728706 | ||||||
chrX:111728796
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2368+491T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111728796 | ||||||
chrX:111728924
|
T | C | 1 | a0001c0002t0001g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2368+619T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111728924 | ||||||
chrX:111728999
|
G | GTTTTTTA | 1 | a0001c0001t0001g0151 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2368+697_2368+703d others(9): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chrX | 111728999 | |||||
chrX:111729247
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2368+942T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729247 | ||||||
chrX:111729296
|
T | C | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2368+991T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729296 | ||||||
chrX:111729398
|
G | GA | 1 | a0001c0001t0001g0100 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2369-989dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chrX | 111729398 | |||||
chrX:111729444
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2369-951G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729444 | ||||||
chrX:111729533
|
T | TGG | 1 | a0001c0017t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2369-862_2369-861i others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729533 | ||||||
chrX:111729597
|
A | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2369-798A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729597 | ||||||
chrX:111729714
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369-681C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729714 | ||||||
chrX:111729726
|
G | A | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(66): Show | 70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.2369-669G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729726 | ||||||
chrX:111729818
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2369-577A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729818 | ||||||
chrX:111729923
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0058a0001c0002t0001g0059others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2369-472T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729923 | ||||||
chrX:111730177
|
A | AT | 2 | a0001c0006t0001g0153a0001c0006t0001g0179 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2369-214dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chrX | 111730177 | |||||
chrX:111730297
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2369-98A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111730297 | ||||||
chrX:111730439
|
C | A | 1 | a0001c0002t0001g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2401+12C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 20/26 | chrX | 111730439 | ||||||
chrX:111730613
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2457+33T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111730613 | ||||||
chrX:111731018
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2457+438C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731018 | ||||||
chrX:111731452
|
A | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2457+872A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731452 | ||||||
chrX:111731588
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2457+1008C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731588 | ||||||
chrX:111731739
|
G | A | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(66): Show | 70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.2457+1159G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731739 | ||||||
chrX:111732013
|
G | A | 7 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0125others(4): Show | 7 | HG01934.hp1 NA18944.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.2457+1433G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732013 | ||||||
chrX:111732150
|
A | G | 2 | a0001c0001t0001g0105a0008c0016t0001g0106 | 2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2457+1570A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732150 | ||||||
chrX:111732370
|
T | C | 1 | a0002c0003t0001g0116 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2457+1790T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732370 | ||||||
chrX:111732770
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2457+2190C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732770 | ||||||
chrX:111732849
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2458-2202A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732849 | ||||||
chrX:111733058
|
C | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(7): Show | 10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2458-1993C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733058 | ||||||
chrX:111733067
|
A | G | 1 | a0006c0013t0001g0163 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2458-1984A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733067 | ||||||
chrX:111733116
|
T | TA | 1 | a0001c0002t0001g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2458-1926dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chrX | 111733116 | |||||
chrX:111733262
|
A | G | 1 | a0005c0015t0001g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2458-1789A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733262 | ||||||
chrX:111733287
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2458-1764C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733287 | ||||||
chrX:111733379
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2458-1672A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733379 | ||||||
chrX:111733409
|
A | G | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2458-1642A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733409 | ||||||
chrX:111733426
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2458-1625G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733426 | ||||||
chrX:111733464
|
T | G | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2458-1587T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733464 | ||||||
chrX:111734127
|
G | GT | 1 | a0001c0001t0001g0114 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2458-918dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chrX | 111734127 | |||||
chrX:111734160
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2458-891C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111734160 | ||||||
chrX:111734589
|
G | A | 1 | a0009c0019t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2458-462G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111734589 | ||||||
chrX:111734667
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2458-384G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111734667 | ||||||
chrX:111735131
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2529+9C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111735131 | ||||||
chrX:111735397
|
C | T | 2 | a0001c0001t0001g0105a0008c0016t0001g0106 | 2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2529+275C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111735397 | ||||||
chrX:111735712
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2529+590G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111735712 | ||||||
chrX:111735946
|
G | GA | 2 | a0001c0017t0001g0042a0002c0005t0001g0077 | 2 | HG02257.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2530-757dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chrX | 111735946 | |||||
chrX:111736404
|
G | T | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2530-310G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111736404 | ||||||
chrX:111736452
|
C | T | 26 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0020others(23): Show | 27 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.2530-262C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111736452 | ||||||
chrX:111736926
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2695+47A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111736926 | ||||||
chrX:111737317
|
C | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+438C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111737317 | ||||||
chrX:111737334
|
T | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0150a0002c0003t0001g0116others(2): Show | 5 | HG01192.hp1 NA18953.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.2695+455T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111737334 | ||||||
chrX:111738135
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2695+1256A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738135 | ||||||
chrX:111738222
|
G | A | 1 | a0001c0002t0001g0022 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2695+1343G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738222 | ||||||
chrX:111738247
|
T | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG01884.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2695+1368T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738247 | ||||||
chrX:111738415
|
G | A | 1 | a0002c0003t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2695+1536G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738415 | ||||||
chrX:111738479
|
G | C | 4 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0033others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+1600G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738479 | ||||||
chrX:111738499
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2695+1620C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738499 | ||||||
chrX:111738797
|
A | G | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+1918A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738797 | ||||||
chrX:111738847
|
G | GAA | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG01884.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2695+1980_2695+198 others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111738847 | |||||
chrX:111738847
|
GA | G | 1 | a0001c0017t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2695+1981delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111738847 | |||||
chrX:111738945
|
A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2695+2066A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738945 | ||||||
chrX:111739369
|
A | C | 1 | a0001c0002t0001g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2695+2490A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739369 | ||||||
chrX:111739397
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0058a0001c0002t0001g0059others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2695+2518A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739397 | ||||||
chrX:111739584
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2695+2705T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739584 | ||||||
chrX:111739855
|
T | C | 1 | a0001c0002t0001g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2695+2976T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739855 | ||||||
chrX:111739877
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2695+2998C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739877 | ||||||
chrX:111740735
|
A | G | 1 | a0001c0002t0001g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2695+3856A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111740735 | ||||||
chrX:111741196
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2696-3472T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741196 | ||||||
chrX:111741204
|
G | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2696-3464G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741204 | ||||||
chrX:111741394
|
A | G | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2696-3274A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741394 | ||||||
chrX:111741406
|
A | G | 1 | a0002c0003t0001g0091 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2696-3262A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741406 | ||||||
chrX:111741782
|
C | T | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2696-2886C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741782 | ||||||
chrX:111741810
|
C | CA | 6 | a0001c0001t0001g0054a0001c0001t0001g0088a0001c0001t0001g0144others(3): Show | 6 | HG01106.hp1 HG02132.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2696-2842dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111741810 | |||||
chrX:111741810
|
CA | C | 27 | a0001c0001t0001g0086a0001c0001t0001g0164a0001c0001t0001g0166others(24): Show | 28 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2696-2842delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111741810 | |||||
chrX:111741825
|
A | T | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2696-2843A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741825 | ||||||
chrX:111742090
|
A | G | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-2578A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742090 | ||||||
chrX:111742440
|
C | CA | 3 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0078 | 3 | HG01106.hp1 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2696-2214dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111742440 | |||||
chrX:111742440
|
CA | C | 1 | a0001c0017t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2696-2214delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111742440 | |||||
chrX:111742653
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2696-2015G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742653 | ||||||
chrX:111742729
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 6 | NA18943.hp1 NA18959.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.2696-1939G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742729 | ||||||
chrX:111742833
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(19): Show | 23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2696-1835G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742833 | ||||||
chrX:111742981
|
A | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2696-1687A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742981 | ||||||
chrX:111743069
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2696-1599C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111743069 | ||||||
chrX:111743752
|
C | G | 25 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0020others(22): Show | 26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2696-916C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111743752 | ||||||
chrX:111743906
|
T | TA | 2 | a0001c0017t0001g0042a0003c0004t0001g0069 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2696-750dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111743906 | |||||
chrX:111743906
|
T | TAA | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(7): Show | 10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2696-751_2696-750d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111743906 | |||||
chrX:111743906
|
TA | T | 2 | a0001c0001t0001g0144a0002c0003t0001g0065 | 2 | HG02132.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2696-750delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111743906 | |||||
chrX:111743916
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2696-752A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111743916 | ||||||
chrX:111744164
|
G | A | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2696-504G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111744164 | ||||||
chrX:111744994
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2932+90G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111744994 | ||||||
chrX:111745767
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932+863A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111745767 | ||||||
chrX:111746130
|
T | TA | 1 | a0001c0001t0001g0117 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2932+1231dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111746130 | |||||
chrX:111746184
|
T | C | 2 | a0001c0006t0001g0153a0001c0006t0001g0179 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2932+1280T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746184 | ||||||
chrX:111746405
|
T | G | 22 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(19): Show | 23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2932+1501T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746405 | ||||||
chrX:111746966
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2932+2062T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746966 | ||||||
chrX:111746977
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2932+2073C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746977 | ||||||
chrX:111747190
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2932+2286G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747190 | ||||||
chrX:111747579
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932+2675C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747579 | ||||||
chrX:111747592
|
T | C | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2932+2688T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747592 | ||||||
chrX:111747636
|
A | G | 1 | a0001c0002t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2932+2732A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747636 | ||||||
chrX:111748478
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2932+3574G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748478 | ||||||
chrX:111748817
|
T | A | 1 | a0001c0002t0001g0019 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2932+3913T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748817 | ||||||
chrX:111748841
|
C | G | 1 | a0001c0001t0001g0137 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2932+3937C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748841 | ||||||
chrX:111748864
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2933-3926A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748864 | ||||||
chrX:111749097
|
CA | C | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2933-3685delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111749097 | |||||
chrX:111749116
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0075 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2933-3674C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749116 | ||||||
chrX:111749145
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2933-3645C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749145 | ||||||
chrX:111749249
|
A | AT | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2933-3532dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111749249 | |||||
chrX:111749485
|
C | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2933-3305C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749485 | ||||||
chrX:111749501
|
C | CA | 19 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0081others(16): Show | 19 | HG00558.hp1 HG01243.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2933-3276dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111749501 | |||||
chrX:111749515
|
C | G | 1 | a0001c0002t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2933-3275C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749515 | ||||||
chrX:111749572
|
A | G | 19 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(16): Show | 19 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2933-3218A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749572 | ||||||
chrX:111749671
|
T | TG | 1 | a0001c0001t0001g0088 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2933-3117dupG | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111749671 | |||||
chrX:111749959
|
CTT | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0136a0011c0020t0001g0006 | 3 | NA18974.hp1 NA19005.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2933-2829_2933-282 others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111749959 | |||||
chrX:111750084
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2933-2706T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111750084 | ||||||
chrX:111750551
|
A | G | 1 | a0003c0014t0001g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2933-2239A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111750551 | ||||||
chrX:111750619
|
AGTATT | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0175 | 2 | HG02074.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.2933-2158_2933-215 others(9): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750619 | |||||
chrX:111750632
|
ATTGT | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2933-2143_2933-214 others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750632 | |||||
chrX:111750656
|
C | CTTAT | 5 | a0001c0001t0001g0133a0001c0001t0001g0144a0001c0001t0001g0171others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933-2107_2933-210 others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750656 | |||||
chrX:111750656
|
CTTAT | C | 3 | a0001c0002t0001g0020a0001c0002t0001g0035a0001c0002t0001g0185 | 3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2933-2107_2933-210 others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750656 | |||||
chrX:111750692
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2933-2098T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111750692 | ||||||
chrX:111751066
|
C | CT | 5 | a0001c0001t0001g0008a0001c0001t0001g0088a0001c0001t0001g0131others(2): Show | 5 | HG00609.hp1 HG03516.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933-1703dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111751066 | |||||
chrX:111751066
|
CT | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(53): Show | 57 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.2933-1703delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111751066 | |||||
chrX:111751066
|
CTT | C | 1 | a0001c0001t0001g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2933-1704_2933-170 others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111751066 | |||||
chrX:111751092
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2933-1698C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751092 | ||||||
chrX:111751342
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2933-1448C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751342 | ||||||
chrX:111751358
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0021others(19): Show | 23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2933-1432C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751358 | ||||||
chrX:111751564
|
G | A | 1 | a0001c0002t0001g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2933-1226G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751564 | ||||||
chrX:111751625
|
C | G | 5 | a0001c0001t0001g0086a0001c0001t0001g0164a0001c0001t0001g0166others(2): Show | 5 | NA18952.hp1 NA18970.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933-1165C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751625 | ||||||
chrX:111751724
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2933-1066T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751724 | ||||||
chrX:111751724
|
T | TA | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2933-1057dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111751724 | |||||
chrX:111751849
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2933-941G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751849 | ||||||
chrX:111752426
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2933-364T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752426 | ||||||
chrX:111752447
|
G | A | 2 | a0001c0001t0001g0043a0004c0010t0001g0046 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2933-343G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752447 | ||||||
chrX:111752485
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2933-305G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752485 | ||||||
chrX:111752576
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2933-214C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752576 | ||||||
chrX:111752733
|
A | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2933-57A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752733 | ||||||
chrX:111753512
|
GT | G | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2973+686delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | 111753512 | |||||
chrX:111753539
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2973+709G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111753539 | ||||||
chrX:111753766
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2973+936A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111753766 | ||||||
chrX:111754008
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2973+1178G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754008 | ||||||
chrX:111754023
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2973+1193A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754023 | ||||||
chrX:111754358
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2973+1528C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754358 | ||||||
chrX:111754360
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2973+1530G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754360 | ||||||
chrX:111754433
|
G | A | 25 | a0001c0002t0001g0001a0001c0002t0001g0019a0001c0002t0001g0020others(22): Show | 26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2973+1603G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754433 | ||||||
chrX:111754965
|
C | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(34): Show | 37 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.2973+2135C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754965 | ||||||
chrX:111755469
|
AAAAG | A | 1 | a0001c0001t0001g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2974-2116_2974-211 others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | 111755469 | |||||
chrX:111755549
|
T | C | 1 | a0001c0002t0001g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2974-2039T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111755549 | ||||||
chrX:111755572
|
A | AAATTTAC others(3): Show |
2 | a0001c0001t0001g0114a0002c0003t0001g0148 | 2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2974-2013_2974-200 others(14): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | 111755572 | |||||
chrX:111755678
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2974-1910A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111755678 | ||||||
chrX:111756152
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(7): Show | 10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2974-1436A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756152 | ||||||
chrX:111756160
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2974-1428G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756160 | ||||||
chrX:111756255
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2974-1333C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756255 | ||||||
chrX:111756261
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(60): Show | 64 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(61): Show |
intron_variant | MODIFIER | c.2974-1327C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756261 | ||||||
chrX:111756262
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2974-1326G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756262 | ||||||
chrX:111756263
|
G | C | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2974-1325G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756263 | ||||||
chrX:111756383
|
A | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0070others(6): Show | 9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2974-1205A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756383 | ||||||
chrX:111756489
|
C | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2974-1099C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756489 | ||||||
chrX:111757248
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2974-340G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111757248 | ||||||
chrX:111757400
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2974-188A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111757400 | ||||||
chrX:111757493
|
A | AT | 7 | a0001c0001t0001g0088a0001c0001t0001g0109a0001c0001t0001g0117others(4): Show | 7 | HG01255.hp1 HG01515.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2974-79dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | 111757493 | |||||
chrX:111757493
|
AT | A | 2 | a0001c0001t0001g0137a0006c0013t0001g0163 | 2 | NA18612.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2974-79delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | 111757493 | |||||
chrX:111757547
|
A | C | 4 | a0003c0004t0001g0010a0003c0004t0001g0067a0003c0004t0001g0068others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2974-41A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111757547 | ||||||
chrX:111758317
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(70): Show | 74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.3148+555G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758317 | ||||||
chrX:111758444
|
A | G | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3148+682A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758444 | ||||||
chrX:111758475
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3148+713C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758475 | ||||||
chrX:111758643
|
AT | A | 1 | a0001c0001t0001g0167 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3148+886delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | 111758643 | |||||
chrX:111758827
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3149-907C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758827 | ||||||
chrX:111759029
|
CT | C | 3 | a0001c0001t0001g0137a0002c0003t0001g0116a0002c0003t0001g0146 | 3 | NA18612.hp1 NA18961.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3149-695delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | 111759029 | |||||
chrX:111759144
|
A | AT | 10 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0088others(7): Show | 10 | HG01928.hp1 HG01943.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.3149-572dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | 111759144 | |||||
chrX:111759144
|
AT | A | 34 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(31): Show | 35 | HG01256.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.3149-572delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | 111759144 | |||||
chrX:111759179
|
CATT | C | 1 | a0002c0009t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3149-552_3149-550d others(5): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | 111759179 | |||||
chrX:111759343
|
G | C | 1 | a0006c0013t0001g0163 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3149-391G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111759343 | ||||||
chrX:111759595
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 6 | NA18943.hp1 NA18959.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.3149-139G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111759595 |