geneid | 5827 |
---|---|
ensemblid | ENSG00000176894.10 |
hgncid | 9716 |
symbol | PXMP2 |
name | peroxisomal membrane protein 2 |
refseq_nuc | NM_018663.3 |
refseq_prot | NP_061133.1 |
ensembl_nuc | ENST00000317479.8 |
ensembl_prot | ENSP00000321271.3 |
mane_status | MANE Select |
chr | chr12 |
start | 132687587 |
end | 132704985 |
strand | + |
ver | v1.2 |
region | chr12:132687587-132704985 |
region5000 | chr12:132682587-132709985 |
regionname0 | PXMP2_chr12_132687587_132704985 |
regionname5000 | PXMP2_chr12_132682587_132709985 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 195 | 347 | 91 | 80 | 117 | 16 | 41 | 81 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0002 | 0/0 | 195 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0003 | 0/0 | 195 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0004 | 0/0 | 200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 588 | 216 | 63 | 44 | 75 | 10 | 23 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0002 | 0/1 | 588 | 92 | 17 | 27 | 27 | 5 | 15 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0003 | 0/0 | 588 | 25 | 1 | 7 | 13 | 1 | 3 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0004 | 0/0 | 588 | 10 | 8 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0005 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0006 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0007 | 0/0 | 588 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0008 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0009 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
c0010 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 383 | 215 | 62 | 44 | 74 | 10 | 24 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
t0002 | 0/1 | 383 | 94 | 20 | 25 | 28 | 5 | 15 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
t0003 | 0/0 | 383 | 25 | 1 | 7 | 13 | 1 | 3 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
t0004 | 0/0 | 383 | 6 | 5 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
t0005 | 0/0 | 383 | 5 | 4 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
t0006 | 0/0 | 383 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
t0007 | 0/0 | 383 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
t0008 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 47 | 9 | 10 | 23 | 0 | 5 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0002 | 0/0 | 33 | 5 | 12 | 14 | 1 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0003 | 0/0 | 24 | 1 | 8 | 11 | 0 | 4 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0004 | 0/0 | 11 | 0 | 5 | 2 | 0 | 4 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0005 | 0/0 | 9 | 0 | 3 | 0 | 4 | 2 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0006 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0009 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0011 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0021 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0025 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0038 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 588 | 216 | 63 | 44 | 75 | 10 | 23 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0002 | 0/1 | 588 | 92 | 17 | 27 | 27 | 5 | 15 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0003 | 0/0 | 588 | 25 | 1 | 7 | 13 | 1 | 3 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0004 | 0/0 | 588 | 10 | 8 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0005 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0008 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0010 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0002c0007 | 0/0 | 588 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0003c0009 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0004c0006 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 970 | 213 | 62 | 44 | 73 | 10 | 23 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0001t0002 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0001t0007 | 0/0 | 970 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0002t0002 | 0/1 | 970 | 90 | 17 | 25 | 27 | 5 | 15 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0002t0006 | 0/0 | 970 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0003t0003 | 0/0 | 970 | 24 | 1 | 7 | 12 | 1 | 3 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0003t0008 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0004t0002 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0004t0004 | 0/0 | 970 | 6 | 5 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0004t0005 | 0/0 | 970 | 3 | 2 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0005t0005 | 0/0 | 970 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0008t0003 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0001c0010t0001 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0002c0007t0001 | 0/0 | 970 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0003c0009t0002 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
a0004c0006t0002 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | copy fasta | chr12 | 132682587 | 132709985 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 46 | 9 | 10 | 22 | 0 | 5 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0003 | 0/0 | 24 | 1 | 8 | 11 | 0 | 4 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0005 | 0/0 | 9 | 0 | 3 | 0 | 4 | 2 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0038 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0002 | 0/0 | 31 | 5 | 10 | 14 | 1 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0004 | 0/0 | 11 | 0 | 5 | 2 | 0 | 4 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0006 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0009 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0025 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0002t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0003t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0004t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0004t0004g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0004t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0004t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0004t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0004t0005g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0005t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0005t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0008t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0001c0010t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0002c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0003c0009t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
a0004c0006t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0009 | EUR | GBR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00280 | hp1 | a0001 | c0003 | t0003 | g0156 | EUR | FIN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00544 | hp2 | a0001 | c0003 | t0003 | g0043 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00639 | hp1 | a0001 | c0003 | t0003 | g0158 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00639 | hp2 | a0001 | c0003 | t0003 | g0147 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01070 | hp1 | a0001 | c0003 | t0003 | g0154 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01071 | hp1 | a0001 | c0003 | t0003 | g0042 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01109 | hp1 | a0001 | c0004 | t0005 | g0010 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01168 | hp1 | a0001 | c0003 | t0003 | g0041 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01169 | hp2 | a0001 | c0003 | t0003 | g0041 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01243 | hp1 | a0001 | c0004 | t0004 | g0027 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01243 | hp2 | a0001 | c0003 | t0003 | g0042 | AMR | PUR | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01257 | hp2 | a0001 | c0002 | t0006 | g0002 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01258 | hp1 | a0001 | c0002 | t0006 | g0002 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | IBS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0052 | EUR | IBS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02027 | hp2 | a0001 | c0003 | t0003 | g0044 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02071 | hp2 | a0001 | c0010 | t0001 | g0103 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | KHV | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0075 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02630 | hp1 | a0001 | c0004 | t0004 | g0079 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0056 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02717 | hp1 | a0001 | c0004 | t0004 | g0027 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02717 | hp2 | a0001 | c0004 | t0005 | g0010 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0023 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02896 | hp1 | a0001 | c0004 | t0004 | g0028 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02897 | hp1 | a0001 | c0004 | t0004 | g0028 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0074 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03139 | hp1 | a0001 | c0005 | t0005 | g0070 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03139 | hp2 | a0004 | c0006 | t0002 | g0051 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03195 | hp1 | a0001 | c0004 | t0002 | g0080 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03225 | hp2 | a0001 | c0004 | t0004 | g0078 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03453 | hp2 | a0001 | c0004 | t0005 | g0010 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03490 | hp1 | a0001 | c0003 | t0003 | g0149 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0150 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03704 | hp1 | a0002 | c0007 | t0001 | g0108 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0025 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0162 | SAS | BEB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0023 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04204 | hp2 | a0001 | c0003 | t0003 | g0040 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | YRI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18942 | hp1 | a0001 | c0003 | t0003 | g0044 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18954 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18977 | hp1 | a0001 | c0003 | t0003 | g0169 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18977 | hp2 | a0001 | c0003 | t0003 | g0046 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18986 | hp2 | a0001 | c0003 | t0008 | g0155 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18989 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18990 | hp1 | a0001 | c0008 | t0003 | g0095 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18998 | hp2 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19000 | hp1 | a0001 | c0003 | t0003 | g0152 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19002 | hp1 | a0001 | c0003 | t0003 | g0047 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | LWK | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | LWK | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19078 | hp2 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19082 | hp1 | a0001 | c0003 | t0003 | g0170 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0043 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19088 | hp2 | a0003 | c0009 | t0002 | g0062 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | YRI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ASW | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0073 | EUR | TSI | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03471 | hp1 | a0001 | c0005 | t0005 | g0071 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | MSL | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | USA | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA18955 | hp2 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20300 | hp1 | a0001 | c0003 | t0003 | g0040 | AFR | USA | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | LWK | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0025 | REF | REF | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | PXMP2_chr12_132682587_132709985 | PXMP2 | chr12 | 132682587 | 132709985 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132687721
|
G | GCCGCGGC others(8): Show |
1 | a0004 | 1 | HG03139.hp2 | conservative_inframe_insertion | MODERATE | c.52_66dupCCGCGGCGGG others(5): Show |
p.Pro18_Leu22dup | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/5 | 151/970 | 67/588 | 23/195 | INFO_REALIGN_3_PRIME | chr12 | 132687721 | |
chr12:132696008
|
T | C | 1 | a0003 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.361T>C | p.Phe121Leu | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/5 | 445/970 | 361/588 | 121/195 | chr12 | 132696008 | ||
chr12:132701287
|
G | A | 1 | a0002 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.437G>A | p.Gly146Glu | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/5 | 521/970 | 437/588 | 146/195 | chr12 | 132701287 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132687688
|
C | T | 1 | a0001c0010 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.18C>T | p.Ser6Ser | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/5 | 102/970 | 18/588 | 6/195 | chr12 | 132687688 | ||
chr12:132687746
|
C | T | 5 | a0001c0002a0001c0003a0001c0005others(2): Show | 121 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(118): Show |
synonymous_variant | LOW | c.76C>T | p.Leu26Leu | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/5 | 160/970 | 76/588 | 26/195 | chr12 | 132687746 | ||
chr12:132695884
|
G | T | 2 | a0001c0003a0001c0008 | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
splice_region_variant&synonymous_variant | LOW | c.237G>T | p.Gly79Gly | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/5 | 321/970 | 237/588 | 79/195 | chr12 | 132695884 | ||
chr12:132695935
|
T | C | 2 | a0001c0004a0001c0005 | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.288T>C | p.His96His | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/5 | 372/970 | 288/588 | 96/195 | chr12 | 132695935 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132687602
|
C | A | 1 | a0001c0004t0004 | 6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/5 | 69 | chr12 | 132687602 | |||||
chr12:132687646
|
C | T | 1 | a0001c0003t0008 | 1 | NA18986.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/5 | 25 | chr12 | 132687646 | |||||
chr12:132704773
|
G | A | 1 | a0001c0002t0006 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 5/5 | 86 | chr12 | 132704773 | |||||
chr12:132704866
|
A | G | 1 | a0001c0001t0007 | 2 | NA18954.hp2 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*179A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 5/5 | 179 | chr12 | 132704866 | |||||
chr12:132704875
|
C | T | 3 | a0001c0004t0004a0001c0004t0005a0001c0005t0005 | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*188C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 5/5 | 188 | chr12 | 132704875 | |||||
chr12:132704876
|
G | A | 9 | a0001c0001t0002a0001c0002t0002a0001c0002t0006others(6): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*189G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 5/5 | 189 | chr12 | 132704876 | |||||
chr12:132704890
|
G | A | 3 | a0001c0003t0003a0001c0003t0008a0001c0008t0003 | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 5/5 | 203 | chr12 | 132704890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:132687798
|
C | CG | 11 | a0001c0001t0001g0021a0001c0001t0001g0163a0001c0001t0001g0164others(8): Show | 13 | HG01175.hp1 HG01978.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+11dupG | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132687798 | |||||
chr12:132687867
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.122+75C>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132687867 | ||||||
chr12:132688035
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.122+243G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688035 | ||||||
chr12:132688119
|
AGGCGCGG others(32): Show |
A | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.122+402_122+440del others(39): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688119 | |||||
chr12:132688149
|
GGGTCTGC others(31): Show |
G | 1 | a0001c0003t0003g0047 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+360_122+397del others(38): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688149 | |||||
chr12:132688154
|
T | C | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.122+362T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688154 | ||||||
chr12:132688156
|
CG | C | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.122+368delG | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688156 | |||||
chr12:132688158
|
G | A | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.122+366G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688158 | ||||||
chr12:132688166
|
G | A | 1 | a0001c0003t0003g0046 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.122+374G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688166 | ||||||
chr12:132688195
|
CGGGGCGC others(656): Show |
C | 6 | a0001c0004t0002g0080a0001c0004t0004g0027a0001c0004t0004g0028others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+426_122+1088de others(1): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688195 | |||||
chr12:132688210
|
G | T | 1 | a0001c0002t0002g0077 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.122+418G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688210 | ||||||
chr12:132688273
|
CGGGGCGC others(578): Show |
C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG02145.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.122+869_123-1018de others(1): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688273 | |||||
chr12:132688279
|
G | A | 63 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(60): Show | 121 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.122+487G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688279 | ||||||
chr12:132688318
|
ACGGGTGA others(305): Show |
A | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.122+557_122+868del | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688318 | |||||
chr12:132688335
|
C | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+543C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688335 | ||||||
chr12:132688337
|
GGGGAGCG others(149): Show |
G | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.122+557_122+712del | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688337 | |||||
chr12:132688345
|
GGTCCTCA others(32): Show |
G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+557_122+595del others(39): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688345 | |||||
chr12:132688410
|
C | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+618C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688410 | ||||||
chr12:132688428
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+636T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688428 | ||||||
chr12:132688429
|
G | C | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+637G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688429 | ||||||
chr12:132688441
|
A | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+649A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688441 | ||||||
chr12:132688452
|
C | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+660C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688452 | ||||||
chr12:132688466
|
C | T | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+674C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688466 | ||||||
chr12:132688467
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+675T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688467 | ||||||
chr12:132688469
|
A | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+677A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688469 | ||||||
chr12:132688470
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+678T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688470 | ||||||
chr12:132688481
|
G | A | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+689G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688481 | ||||||
chr12:132688493
|
A | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+701A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688493 | ||||||
chr12:132688532
|
A | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+740A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688532 | ||||||
chr12:132688545
|
G | T | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+753G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688545 | ||||||
chr12:132688546
|
C | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+754C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688546 | ||||||
chr12:132688591
|
A | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+799A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688591 | ||||||
chr12:132688597
|
A | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+805A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688597 | ||||||
chr12:132688597
|
AAAGACAG others(71): Show |
A | 1 | a0001c0001t0001g0146 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.122+816_122+893del others(78): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688597 | |||||
chr12:132688610
|
A | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+818A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688610 | ||||||
chr12:132688626
|
T | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+834T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688626 | ||||||
chr12:132688629
|
T | C | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+837T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688629 | ||||||
chr12:132688629
|
T | TGCGGGTG others(71): Show |
1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.122+1050_122+1127d others(80): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688629 | |||||
chr12:132688629
|
TGCGGGTG others(71): Show |
T | 4 | a0001c0001t0001g0045a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG03017.hp1 HG03492.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+1050_122+1127d others(80): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688629 | |||||
chr12:132688647
|
C | G | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.122+855C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688647 | ||||||
chr12:132688662
|
G | T | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.122+870G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688662 | ||||||
chr12:132688663
|
C | G | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.122+871C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688663 | ||||||
chr12:132688667
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122+875G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688667 | ||||||
chr12:132688669
|
A | G | 62 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(59): Show | 120 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.122+877A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688669 | ||||||
chr12:132688686
|
G | C | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.122+894G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688686 | ||||||
chr12:132688701
|
T | G | 62 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(59): Show | 120 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.122+909T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688701 | ||||||
chr12:132688702
|
G | C | 62 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(59): Show | 120 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.122+910G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688702 | ||||||
chr12:132688725
|
C | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+933C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688725 | ||||||
chr12:132688746
|
CACGGGTG others(17): Show |
C | 1 | a0001c0003t0003g0046 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.122+955_122+978del others(24): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688746 | ||||||
chr12:132688747
|
A | G | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.122+955A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688747 | ||||||
chr12:132688764
|
G | C | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.122+972G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688764 | ||||||
chr12:132688779
|
T | C | 1 | a0001c0003t0003g0047 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+987T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688779 | ||||||
chr12:132688779
|
T | G | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.122+987T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688779 | ||||||
chr12:132688780
|
G | C | 20 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.122+988G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688780 | ||||||
chr12:132688786
|
G | A | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+994G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688786 | ||||||
chr12:132688786
|
GCGGGTGA others(32): Show |
G | 3 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0076 | 3 | HG02615.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.122+1011_122+1049d others(41): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688786 | |||||
chr12:132688803
|
C | G | 60 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(57): Show | 118 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.122+1011C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688803 | ||||||
chr12:132688818
|
G | T | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+1026G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688818 | ||||||
chr12:132688819
|
C | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+1027C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688819 | ||||||
chr12:132688819
|
CGGGGCAC others(32): Show |
C | 39 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(36): Show | 92 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.122+1033_122+1071d others(41): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688819 | |||||
chr12:132688825
|
A | G | 21 | a0001c0002t0002g0153a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+1033A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688825 | ||||||
chr12:132688857
|
T | G | 22 | a0001c0001t0001g0088a0001c0002t0002g0153a0001c0003t0003g0040others(19): Show | 27 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.122+1065T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688857 | ||||||
chr12:132688858
|
G | C | 22 | a0001c0001t0001g0088a0001c0002t0002g0153a0001c0003t0003g0040others(19): Show | 27 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.122+1066G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688858 | ||||||
chr12:132688881
|
C | G | 3 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0076 | 3 | HG02615.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.122+1089C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132688881 | ||||||
chr12:132688903
|
ACGGGTGA others(305): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.122+1143_123-1017d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132688903 | |||||
chr12:132689020
|
G | GCGGGTAA others(227): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0168 | 3 | NA18952.hp2 NA19009.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.123-1213_123-1212i others(236): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132689020 | |||||
chr12:132689034
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0090 | 5 | HG02559.hp2 HG02965.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1229G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689034 | ||||||
chr12:132689137
|
G | A | 3 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0147 | 5 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-1126G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689137 | ||||||
chr12:132689150
|
G | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-1113G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689150 | ||||||
chr12:132689154
|
G | C | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-1109G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689154 | ||||||
chr12:132689156
|
G | A | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-1107G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689156 | ||||||
chr12:132689171
|
G | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.123-1092G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689171 | ||||||
chr12:132689289
|
GGGCGCGG others(8): Show |
G | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123-964_123-950del others(15): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 132689289 | |||||
chr12:132689309
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123-954C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689309 | ||||||
chr12:132689335
|
G | A | 3 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079 | 4 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-928G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689335 | ||||||
chr12:132689559
|
C | T | 1 | a0001c0003t0003g0047 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.123-704C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689559 | ||||||
chr12:132689589
|
C | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-674C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689589 | ||||||
chr12:132689617
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0168 | 2 | NA19009.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.123-646C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689617 | ||||||
chr12:132689626
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123-637T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689626 | ||||||
chr12:132689709
|
T | C | 1 | a0001c0001t0001g0032 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.123-554T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132689709 | ||||||
chr12:132690069
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0094 | 2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.123-194T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132690069 | ||||||
chr12:132690076
|
C | G | 1 | a0001c0002t0002g0026 | 2 | HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.123-187C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132690076 | ||||||
chr12:132690227
|
G | T | 2 | a0001c0002t0002g0025a0001c0002t0002g0073 | 3 | HG03704.hp2 NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.123-36G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 1/4 | chr12 | 132690227 | ||||||
chr12:132690503
|
A | G | 1 | a0001c0004t0005g0010 | 3 | HG01109.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.236+127A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132690503 | ||||||
chr12:132690512
|
A | G | 1 | a0001c0002t0002g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.236+136A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132690512 | ||||||
chr12:132690578
|
CT | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(75): Show | 148 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.236+211delT | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132690578 | |||||
chr12:132690734
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.236+358A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132690734 | ||||||
chr12:132690763
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.236+387T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132690763 | ||||||
chr12:132690776
|
A | G | 3 | a0001c0003t0003g0046a0001c0003t0003g0156a0001c0003t0003g0157 | 3 | HG00280.hp1 NA18977.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.236+400A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132690776 | ||||||
chr12:132690857
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+481A>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132690857 | ||||||
chr12:132691050
|
A | T | 1 | a0001c0003t0008g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.236+674A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132691050 | ||||||
chr12:132691051
|
AT | A | 56 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0029others(53): Show | 115 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.236+693delT | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132691051 | |||||
chr12:132691051
|
ATT | A | 21 | a0001c0002t0002g0052a0001c0002t0002g0053a0001c0003t0003g0040others(18): Show | 27 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.236+692_236+693del others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132691051 | |||||
chr12:132691053
|
T | A | 1 | a0001c0003t0008g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.236+677T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132691053 | ||||||
chr12:132691107
|
G | A | 1 | a0001c0010t0001g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.236+731G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132691107 | ||||||
chr12:132691242
|
G | A | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.236+866G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132691242 | ||||||
chr12:132691343
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.236+967T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132691343 | ||||||
chr12:132691763
|
G | A | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.236+1387G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132691763 | ||||||
chr12:132691801
|
C | T | 1 | a0001c0002t0002g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.236+1425C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132691801 | ||||||
chr12:132692006
|
A | G | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.236+1630A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692006 | ||||||
chr12:132692035
|
TGCCAGTT others(91): Show |
T | 1 | a0001c0002t0002g0054 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.236+1660_236+1757d others(100): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692035 | ||||||
chr12:132692105
|
TGCCAGTT others(18): Show |
T | 1 | a0001c0001t0001g0020 | 3 | HG01884.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.236+1754_236+1778d others(27): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692105 | |||||
chr12:132692133
|
CAGTT | C | 40 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(37): Show | 93 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.236+1765_236+1768d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692133 | |||||
chr12:132692136
|
T | C | 1 | a0001c0002t0002g0054 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.236+1760T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692136 | ||||||
chr12:132692137
|
T | C | 1 | a0001c0002t0002g0054 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.236+1761T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692137 | ||||||
chr12:132692257
|
T | TAGTTAGT others(186): Show |
1 | a0001c0001t0001g0140 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.236+1966_236+1967i others(195): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692257 | |||||
chr12:132692275
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.236+1899A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692275 | ||||||
chr12:132692299
|
TGCCAGTT others(92): Show |
T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2006_236+2104d others(101): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692299 | |||||
chr12:132692343
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0098a0001c0001t0001g0105others(2): Show | 6 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+1967G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692343 | ||||||
chr12:132692343
|
G | T | 70 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(67): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.236+1967G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692343 | ||||||
chr12:132692368
|
T | G | 70 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(67): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.236+1992T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692368 | ||||||
chr12:132692373
|
T | TGCCAGTT others(190): Show |
18 | a0001c0003t0003g0040a0001c0003t0003g0042a0001c0003t0003g0043others(15): Show | 22 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.236+2015_236+2016i others(199): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692373 | |||||
chr12:132692373
|
T | TGCCAGTT others(189): Show |
1 | a0001c0003t0008g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.236+2015_236+2016i others(198): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692373 | |||||
chr12:132692382
|
GTTAGTGA others(92): Show |
G | 40 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(37): Show | 86 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.236+2031_236+2129d others(101): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692382 | |||||
chr12:132692392
|
T | G | 11 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0003t0003g0041others(8): Show | 23 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.236+2016T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692392 | ||||||
chr12:132692398
|
AGCCAGTT others(164): Show |
A | 2 | a0001c0002t0002g0006a0001c0002t0002g0009 | 9 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.236+2031_236+2201d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692398 | |||||
chr12:132692407
|
A | G | 28 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(25): Show | 37 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.236+2031A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692407 | ||||||
chr12:132692417
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.236+2041T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692417 | ||||||
chr12:132692417
|
T | G | 9 | a0001c0003t0003g0041a0001c0003t0003g0157a0001c0004t0004g0027others(6): Show | 14 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.236+2041T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692417 | ||||||
chr12:132692419
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.236+2043C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692419 | ||||||
chr12:132692421
|
T | TTGCCAGT others(115): Show |
1 | a0001c0003t0003g0041 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.236+2046_236+2047i others(124): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692421 | |||||
chr12:132692422
|
TA | T | 8 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+2047delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692422 | ||||||
chr12:132692423
|
A | T | 1 | a0001c0003t0003g0041 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.236+2047A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692423 | ||||||
chr12:132692432
|
G | C | 8 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+2056G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692432 | ||||||
chr12:132692442
|
G | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0167a0001c0003t0003g0041 | 4 | HG01168.hp1 HG01169.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+2066G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692442 | ||||||
chr12:132692447
|
T | G | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.236+2071T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692447 | ||||||
chr12:132692447
|
TA | T | 7 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+2072delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692447 | ||||||
chr12:132692451
|
CAGTT | C | 2 | a0001c0001t0001g0035a0002c0007t0001g0108 | 3 | HG02129.hp2 HG02155.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.236+2083_236+2086d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692451 | |||||
chr12:132692458
|
T | G | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.236+2082T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692458 | ||||||
chr12:132692471
|
T | TG | 8 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+2095_236+2096i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692471 | ||||||
chr12:132692472
|
T | A | 8 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+2096T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692472 | ||||||
chr12:132692481
|
A | G | 27 | a0001c0003t0003g0040a0001c0003t0003g0042a0001c0003t0003g0043others(24): Show | 35 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.236+2105A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692481 | ||||||
chr12:132692482
|
T | G | 8 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+2106T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692482 | ||||||
chr12:132692491
|
T | G | 59 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(56): Show | 109 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.236+2115T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692491 | ||||||
chr12:132692495
|
T | TTGCCAGT others(455): Show |
1 | a0001c0003t0003g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.236+2120_236+2121i others(464): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692495 | |||||
chr12:132692495
|
T | TTGCCAGT others(455): Show |
17 | a0001c0003t0003g0040a0001c0003t0003g0042a0001c0003t0003g0043others(14): Show | 21 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.236+2120_236+2121i others(464): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692495 | |||||
chr12:132692495
|
T | TTGCCAGT others(454): Show |
1 | a0001c0003t0008g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.236+2120_236+2121i others(463): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692495 | |||||
chr12:132692496
|
T | G | 8 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+2120T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692496 | ||||||
chr12:132692497
|
A | T | 19 | a0001c0003t0003g0040a0001c0003t0003g0042a0001c0003t0003g0043others(16): Show | 23 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.236+2121A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692497 | ||||||
chr12:132692507
|
T | G | 7 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+2131T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692507 | ||||||
chr12:132692516
|
T | G | 41 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(38): Show | 87 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.236+2140T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692516 | ||||||
chr12:132692516
|
TCCCTTGC others(17): Show |
T | 7 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 15 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.236+2164_236+2187d others(26): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692516 | |||||
chr12:132692520
|
T | TG | 7 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+2144_236+2145i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692520 | ||||||
chr12:132692521
|
T | A | 7 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+2145T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692521 | ||||||
chr12:132692521
|
T | TA | 19 | a0001c0003t0003g0040a0001c0003t0003g0042a0001c0003t0003g0043others(16): Show | 23 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.236+2145_236+2146i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692521 | ||||||
chr12:132692521
|
T | TAGCCAGT others(826): Show |
1 | a0001c0003t0003g0041 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.236+2145_236+2146i others(835): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692521 | ||||||
chr12:132692530
|
G | C | 40 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(37): Show | 86 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.236+2154G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692530 | ||||||
chr12:132692531
|
T | G | 7 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+2155T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692531 | ||||||
chr12:132692540
|
G | T | 20 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.236+2164G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692540 | ||||||
chr12:132692553
|
AGTTAGTG others(40): Show |
A | 2 | a0001c0002t0002g0022a0001c0002t0002g0055 | 3 | HG00738.hp2 HG03490.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.236+2178_236+2224d others(49): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692553 | ||||||
chr12:132692556
|
TAGTGAGC others(42): Show |
T | 38 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0023others(35): Show | 83 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.236+2188_236+2236d others(51): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692556 | |||||
chr12:132692564
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0102others(8): Show | 18 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.236+2188A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692564 | ||||||
chr12:132692564
|
A | T | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.236+2188A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692564 | ||||||
chr12:132692568
|
TTGCCAGT others(276): Show |
T | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.236+2194_236+2476d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692568 | |||||
chr12:132692576
|
TAGTTAGT others(22): Show |
T | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.236+2204_236+2232d others(31): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692576 | |||||
chr12:132692587
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.236+2211C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692587 | ||||||
chr12:132692604
|
TA | T | 9 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0022others(6): Show | 21 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.236+2230delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692604 | |||||
chr12:132692613
|
G | T | 44 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(41): Show | 97 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.236+2237G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692613 | ||||||
chr12:132692618
|
T | G | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.236+2242T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692618 | ||||||
chr12:132692629
|
A | G | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.236+2253A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692629 | ||||||
chr12:132692629
|
A | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0102others(7): Show | 17 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.236+2253A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692629 | ||||||
chr12:132692630
|
T | TA | 3 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0102 | 6 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+2255dupA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692630 | |||||
chr12:132692638
|
G | T | 44 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(41): Show | 97 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.236+2262G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692638 | ||||||
chr12:132692642
|
T | TTGCCAGT others(82): Show |
1 | a0001c0004t0004g0028 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+2267_236+2268i others(91): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692642 | |||||
chr12:132692643
|
T | G | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.236+2267T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692643 | ||||||
chr12:132692643
|
TA | T | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2268delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692643 | ||||||
chr12:132692644
|
A | T | 1 | a0001c0004t0004g0028 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+2268A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692644 | ||||||
chr12:132692647
|
CAGTT | C | 5 | a0001c0001t0001g0099a0001c0004t0004g0027a0001c0004t0004g0078others(2): Show | 8 | HG00099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+2279_236+2282d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692647 | |||||
chr12:132692654
|
T | G | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.236+2278T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692654 | ||||||
chr12:132692663
|
G | T | 48 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(45): Show | 104 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.236+2287G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692663 | ||||||
chr12:132692668
|
T | G | 42 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(39): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.236+2292T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692668 | ||||||
chr12:132692684
|
G | GAGCGCCC others(6): Show |
1 | a0001c0004t0004g0028 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+2317_236+2318i others(15): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692684 | |||||
chr12:132692688
|
G | T | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2312G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692688 | ||||||
chr12:132692693
|
T | TA | 24 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0081others(21): Show | 32 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.236+2317_236+2318i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692693 | ||||||
chr12:132692700
|
TAGTTAGT others(38): Show |
T | 6 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+2336_236+2380d others(47): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692700 | |||||
chr12:132692712
|
A | G | 44 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(41): Show | 98 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.236+2336A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692712 | ||||||
chr12:132692730
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.236+2354G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692730 | ||||||
chr12:132692736
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2360T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692736 | ||||||
chr12:132692745
|
C | CAGTT | 8 | a0001c0002t0002g0048a0001c0002t0002g0049a0001c0002t0002g0050others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+2373_236+2376d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692745 | |||||
chr12:132692747
|
G | A | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2371G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692747 | ||||||
chr12:132692748
|
TTAGTGAG others(10): Show |
T | 32 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(29): Show | 85 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.236+2377_236+2393d others(19): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692748 | |||||
chr12:132692749
|
TAGTGAGC others(218): Show |
T | 1 | a0001c0002t0002g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.236+2377_236+2601d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692749 | |||||
chr12:132692752
|
TGAGCTCC others(288): Show |
T | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.236+2377_236+2671d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692752 | ||||||
chr12:132692757
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2381T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692757 | ||||||
chr12:132692763
|
AGCTAGTT others(13): Show |
A | 8 | a0001c0002t0002g0048a0001c0002t0002g0049a0001c0002t0002g0050others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+2390_236+2409d others(22): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692763 | |||||
chr12:132692766
|
T | C | 6 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+2390T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692766 | ||||||
chr12:132692773
|
A | T | 39 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(36): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.236+2397A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692773 | ||||||
chr12:132692778
|
T | G | 7 | a0001c0001t0001g0081a0001c0004t0004g0027a0001c0004t0004g0078others(4): Show | 10 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+2402T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692778 | ||||||
chr12:132692783
|
T | TA | 33 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(30): Show | 86 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.236+2407_236+2408i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692783 | ||||||
chr12:132692794
|
T | TA | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2419dupA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692794 | |||||
chr12:132692802
|
T | G | 47 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(44): Show | 103 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+2426T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692802 | ||||||
chr12:132692806
|
T | TTGCCAGT others(91): Show |
11 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+2431_236+2432i others(100): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692806 | |||||
chr12:132692807
|
TA | T | 49 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(46): Show | 104 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.236+2432delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692807 | ||||||
chr12:132692808
|
A | AGTCAGTT others(67): Show |
1 | a0001c0003t0003g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.236+2433_236+2434i others(76): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692808 | |||||
chr12:132692808
|
A | T | 11 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+2432A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692808 | ||||||
chr12:132692827
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2451T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692827 | ||||||
chr12:132692827
|
T | G | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2451T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692827 | ||||||
chr12:132692833
|
A | AGTCAGTT others(185): Show |
8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+2458_236+2459i others(194): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692833 | |||||
chr12:132692836
|
C | CAGTT | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.236+2464_236+2467d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692836 | |||||
chr12:132692844
|
G | T | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2468G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692844 | ||||||
chr12:132692848
|
T | G | 52 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(49): Show | 110 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.236+2472T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692848 | ||||||
chr12:132692853
|
T | A | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.236+2477T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692853 | ||||||
chr12:132692859
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2483T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692859 | ||||||
chr12:132692867
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2491T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692867 | ||||||
chr12:132692872
|
T | A | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.236+2496T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692872 | ||||||
chr12:132692872
|
T | G | 12 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(9): Show | 17 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.236+2496T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692872 | ||||||
chr12:132692879
|
CCAGTTAG others(18): Show |
C | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.236+2520_236+2544d others(27): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692879 | |||||
chr12:132692896
|
T | G | 30 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(27): Show | 76 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.236+2520T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692896 | ||||||
chr12:132692901
|
TAGTCAGT others(272): Show |
T | 30 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(27): Show | 76 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.236+2526_237-2704d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692901 | ||||||
chr12:132692904
|
T | C | 16 | a0001c0001t0001g0081a0001c0003t0003g0042a0001c0003t0003g0043others(13): Show | 21 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.236+2528T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692904 | ||||||
chr12:132692905
|
CAGTT | C | 5 | a0001c0001t0001g0032a0001c0004t0004g0027a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+2537_236+2540d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692905 | |||||
chr12:132692905
|
CAGTTAGT others(498): Show |
C | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.236+2545_237-2459d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692905 | |||||
chr12:132692921
|
G | T | 13 | a0001c0001t0001g0081a0001c0003t0003g0042a0001c0003t0003g0043others(10): Show | 18 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.236+2545G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692921 | ||||||
chr12:132692926
|
T | TA | 6 | a0001c0001t0001g0081a0001c0003t0003g0157a0001c0004t0004g0027others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+2550_236+2551i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692926 | ||||||
chr12:132692929
|
C | CAGTTAGT others(257): Show |
12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.236+2588_236+2589i others(266): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692929 | |||||
chr12:132692929
|
C | CAGTTAGT others(164): Show |
8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+2560_236+2561i others(173): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692929 | |||||
chr12:132692929
|
C | T | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2553C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692929 | ||||||
chr12:132692933
|
TAGTGAGC others(34): Show |
T | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.236+2561_236+2601d others(43): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692933 | |||||
chr12:132692936
|
T | A | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2560T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692936 | ||||||
chr12:132692941
|
G | T | 15 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(12): Show | 25 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.236+2565G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692941 | ||||||
chr12:132692946
|
T | TA | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.236+2570_236+2571i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692946 | ||||||
chr12:132692949
|
CAGTTAGT others(199): Show |
C | 1 | a0001c0004t0004g0028 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+2595_237-2708d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692949 | |||||
chr12:132692971
|
AGCCAGTT others(13): Show |
A | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.236+2610_236+2629d others(22): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692971 | |||||
chr12:132692973
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2597C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692973 | ||||||
chr12:132692974
|
C | CAGTT | 24 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(21): Show | 32 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.236+2602_236+2605d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692974 | |||||
chr12:132692974
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2598C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692974 | ||||||
chr12:132692991
|
T | TA | 5 | a0001c0002t0002g0056a0001c0004t0004g0027a0001c0004t0004g0078others(2): Show | 8 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+2615_236+2616i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692991 | ||||||
chr12:132692993
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2617C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692993 | ||||||
chr12:132692994
|
C | CAGTT | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.236+2622_236+2625d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132692994 | |||||
chr12:132692994
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2618C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132692994 | ||||||
chr12:132693006
|
G | T | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2630G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693006 | ||||||
chr12:132693022
|
TA | T | 6 | a0001c0001t0001g0081a0001c0002t0002g0056a0001c0004t0004g0027others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+2648delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693022 | |||||
chr12:132693031
|
G | A | 1 | a0001c0002t0002g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.236+2655G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693031 | ||||||
chr12:132693031
|
G | T | 6 | a0001c0001t0001g0081a0001c0002t0002g0056a0001c0004t0004g0027others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+2655G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693031 | ||||||
chr12:132693036
|
TA | T | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2661delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693036 | ||||||
chr12:132693043
|
TTAGA | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0081others(1): Show | 9 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+2671_236+2674d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693043 | |||||
chr12:132693047
|
A | T | 15 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(12): Show | 25 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.236+2671A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693047 | ||||||
chr12:132693056
|
G | T | 7 | a0001c0001t0001g0081a0001c0003t0003g0157a0001c0004t0002g0080others(4): Show | 10 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+2680G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693056 | ||||||
chr12:132693064
|
C | T | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2688C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693064 | ||||||
chr12:132693065
|
CAGTT | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0090others(2): Show | 7 | HG02559.hp2 HG02809.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+2697_236+2700d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693065 | |||||
chr12:132693073
|
TAGTG | T | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.236+2700_236+2703d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693073 | |||||
chr12:132693081
|
G | T | 2 | a0001c0002t0002g0056a0001c0004t0002g0080 | 2 | HG02698.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.236+2705G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693081 | ||||||
chr12:132693086
|
T | TA | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.236+2710_236+2711i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693086 | ||||||
chr12:132693089
|
CAGTT | C | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+2721_236+2724d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693089 | |||||
chr12:132693105
|
A | G | 18 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(15): Show | 28 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.236+2729A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693105 | ||||||
chr12:132693105
|
A | T | 2 | a0001c0001t0001g0081a0001c0003t0003g0157 | 2 | HG02145.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.236+2729A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693105 | ||||||
chr12:132693112
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2736C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693112 | ||||||
chr12:132693113
|
CAGTTAGT others(35): Show |
C | 3 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079 | 4 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-2749_237-2708d others(44): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693113 | |||||
chr12:132693113
|
CAGTTAGT others(63): Show |
C | 1 | a0001c0002t0002g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.236+2745_237-2694d others(72): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693113 | |||||
chr12:132693129
|
T | G | 3 | a0001c0001t0001g0081a0001c0003t0003g0157a0001c0004t0005g0010 | 5 | HG01109.hp1 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+2753T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693129 | ||||||
chr12:132693134
|
TA | T | 3 | a0001c0001t0001g0081a0001c0003t0003g0157a0001c0004t0005g0010 | 5 | HG01109.hp1 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-2749delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693134 | ||||||
chr12:132693138
|
CAGTTAGT others(10): Show |
C | 1 | a0001c0004t0005g0010 | 3 | HG01109.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.237-2738_237-2722d others(19): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693138 | |||||
chr12:132693138
|
CAGTTAGT others(38): Show |
C | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-2726_237-2682d others(47): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693138 | |||||
chr12:132693138
|
CAGTTAGT others(179): Show |
C | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.237-2734_237-2549d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693138 | |||||
chr12:132693150
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2734T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693150 | ||||||
chr12:132693158
|
T | C | 30 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(27): Show | 42 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.237-2726T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693158 | ||||||
chr12:132693166
|
T | A | 30 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(27): Show | 42 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.237-2718T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693166 | ||||||
chr12:132693171
|
T | G | 6 | a0001c0001t0001g0081a0001c0004t0004g0027a0001c0004t0004g0028others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-2713T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693171 | ||||||
chr12:132693182
|
T | C | 30 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(27): Show | 76 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.237-2702T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693182 | ||||||
chr12:132693183
|
T | C | 30 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(27): Show | 76 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.237-2701T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693183 | ||||||
chr12:132693183
|
T | TAGTTACT others(132): Show |
16 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(13): Show | 19 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-2696_237-2695i others(141): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693183 | |||||
chr12:132693185
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2699G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693185 | ||||||
chr12:132693189
|
G | C | 6 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0150others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-2695G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693189 | ||||||
chr12:132693195
|
T | G | 16 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(13): Show | 19 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-2689T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693195 | ||||||
chr12:132693201
|
A | AGCCAGTT others(17): Show |
16 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(13): Show | 19 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-2665_237-2664i others(26): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693201 | |||||
chr12:132693219
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-2665C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693219 | ||||||
chr12:132693220
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2664T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693220 | ||||||
chr12:132693225
|
TA | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2658delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693225 | ||||||
chr12:132693228
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2656C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693228 | ||||||
chr12:132693229
|
C | CAGTT | 16 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(13): Show | 19 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-2651_237-2648d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693229 | |||||
chr12:132693229
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2655C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693229 | ||||||
chr12:132693233
|
TAGTGAGC others(9): Show |
T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2647_237-2632d others(18): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693233 | |||||
chr12:132693240
|
CTCCCTTG others(13): Show |
C | 32 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(29): Show | 78 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-2643_237-2624d others(22): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693240 | ||||||
chr12:132693241
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2643T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693241 | ||||||
chr12:132693243
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0033 | 7 | HG01106.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-2641C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693243 | ||||||
chr12:132693249
|
C | CAGTT | 16 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(13): Show | 19 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-2631_237-2628d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693249 | |||||
chr12:132693249
|
C | CAGTTAGT others(167): Show |
1 | a0001c0003t0003g0169 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.237-2628_237-2627i others(176): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693249 | |||||
chr12:132693249
|
C | CAGTTAGT others(164): Show |
5 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0150others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-2628_237-2627i others(173): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693249 | |||||
chr12:132693249
|
CAGTTAGT others(154): Show |
C | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2627_237-2467d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693249 | |||||
chr12:132693257
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2627G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693257 | ||||||
chr12:132693260
|
T | C | 25 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(22): Show | 34 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.237-2624T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693260 | ||||||
chr12:132693286
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2598G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693286 | ||||||
chr12:132693294
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2590C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693294 | ||||||
chr12:132693302
|
A | T | 33 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(30): Show | 79 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.237-2582A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693302 | ||||||
chr12:132693311
|
G | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2573G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693311 | ||||||
chr12:132693328
|
TAGTG | T | 32 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(29): Show | 78 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-2553_237-2550d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693328 | |||||
chr12:132693336
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.237-2548G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693336 | ||||||
chr12:132693341
|
T | TA | 21 | a0001c0001t0001g0081a0001c0003t0003g0040a0001c0003t0003g0041others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.237-2543_237-2542i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693341 | ||||||
chr12:132693344
|
CAGTTAGT others(59): Show |
C | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-2524_237-2459d others(68): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693344 | |||||
chr12:132693360
|
A | G | 32 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(29): Show | 78 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-2524A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693360 | ||||||
chr12:132693360
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2524A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693360 | ||||||
chr12:132693384
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2500T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693384 | ||||||
chr12:132693392
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2492C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693392 | ||||||
chr12:132693392
|
CCAGTTAG others(14): Show |
C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2491_237-2471d others(23): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693392 | ||||||
chr12:132693393
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2491C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693393 | ||||||
chr12:132693405
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2479T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693405 | ||||||
chr12:132693413
|
T | C | 51 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(48): Show | 102 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.237-2471T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693413 | ||||||
chr12:132693421
|
T | A | 56 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(53): Show | 111 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.237-2463T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693421 | ||||||
chr12:132693455
|
T | G | 1 | a0001c0001t0001g0039 | 2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.237-2429T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693455 | ||||||
chr12:132693458
|
C | T | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2426C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693458 | ||||||
chr12:132693475
|
T | G | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2409T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693475 | ||||||
chr12:132693480
|
TA | T | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2403delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693480 | ||||||
chr12:132693484
|
C | CAGTTAGT others(17): Show |
12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2358_237-2335d others(26): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693484 | |||||
chr12:132693496
|
T | G | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2388T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693496 | ||||||
chr12:132693507
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2377T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693507 | ||||||
chr12:132693515
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2369T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693515 | ||||||
chr12:132693520
|
T | G | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2364T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693520 | ||||||
chr12:132693552
|
T | C | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2332T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693552 | ||||||
chr12:132693557
|
TAGTTAGT others(61): Show |
T | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-2323_237-2256d others(70): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693557 | |||||
chr12:132693561
|
TAGTGAGC others(57): Show |
T | 2 | a0001c0004t0004g0028a0001c0004t0005g0010 | 5 | HG01109.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-2259_237-2196d others(66): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693561 | |||||
chr12:132693569
|
G | T | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2315G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693569 | ||||||
chr12:132693577
|
C | CAGTT | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2303_237-2300d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693577 | |||||
chr12:132693577
|
C | CAGTTAGT others(17): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0094others(1): Show | 6 | HG01891.hp2 HG01934.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-2283_237-2260d others(26): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693577 | |||||
chr12:132693589
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2295G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693589 | ||||||
chr12:132693601
|
TAGTTAGT others(33): Show |
T | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.237-2259_237-2220d others(42): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693601 | |||||
chr12:132693613
|
G | T | 19 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(16): Show | 28 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.237-2271G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693613 | ||||||
chr12:132693613
|
GCCCTTGC others(106): Show |
G | 3 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079 | 4 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-2259_237-2147d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693613 | |||||
chr12:132693613
|
GCCCTTGC others(204): Show |
G | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-2259_237-2049d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693613 | |||||
chr12:132693617
|
TTGCCAGT others(12): Show |
T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2265_237-2247d others(21): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693617 | |||||
chr12:132693618
|
T | TA | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-2266_237-2265i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693618 | ||||||
chr12:132693621
|
C | CAGTT | 17 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(14): Show | 26 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.237-2260_237-2259i others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693621 | |||||
chr12:132693621
|
C | CAGTTAGT others(22): Show |
12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2260_237-2259i others(31): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693621 | |||||
chr12:132693624
|
TCAGTGAG others(9): Show |
T | 2 | a0001c0004t0002g0080a0004c0006t0002g0051 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.237-2255_237-2240d others(18): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693624 | |||||
chr12:132693625
|
C | T | 29 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(26): Show | 41 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.237-2259C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693625 | ||||||
chr12:132693633
|
G | T | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2251G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693633 | ||||||
chr12:132693638
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2246T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693638 | ||||||
chr12:132693641
|
C | CAGTT | 20 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.237-2239_237-2236d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693641 | |||||
chr12:132693641
|
C | T | 2 | a0001c0004t0002g0080a0004c0006t0002g0051 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.237-2243C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693641 | ||||||
chr12:132693653
|
G | A | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2231G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693653 | ||||||
chr12:132693653
|
G | T | 2 | a0001c0001t0001g0081a0001c0004t0002g0080 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.237-2231G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693653 | ||||||
chr12:132693664
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2220T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693664 | ||||||
chr12:132693672
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2212T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693672 | ||||||
chr12:132693677
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2207G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693677 | ||||||
chr12:132693691
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.237-2193G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693691 | ||||||
chr12:132693693
|
T | TA | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2190dupA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693693 | |||||
chr12:132693701
|
T | A | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.237-2183T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693701 | ||||||
chr12:132693701
|
T | G | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2183T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693701 | ||||||
chr12:132693710
|
CAGTT | C | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2166_237-2163d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693710 | |||||
chr12:132693717
|
T | A | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2167T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693717 | ||||||
chr12:132693726
|
T | G | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.237-2158T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693726 | ||||||
chr12:132693731
|
T | TA | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2153_237-2152i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693731 | ||||||
chr12:132693731
|
TGCC | T | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2152_237-2150d others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693731 | ||||||
chr12:132693737
|
T | C | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2147T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693737 | ||||||
chr12:132693738
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2146T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693738 | ||||||
chr12:132693745
|
T | A | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2139T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693745 | ||||||
chr12:132693750
|
T | A | 32 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(29): Show | 78 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-2134T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693750 | ||||||
chr12:132693750
|
T | G | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.237-2134T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693750 | ||||||
chr12:132693755
|
TA | T | 50 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(47): Show | 105 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.237-2128delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693755 | ||||||
chr12:132693766
|
T | A | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.237-2118T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693766 | ||||||
chr12:132693770
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-2114T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693770 | ||||||
chr12:132693775
|
G | A | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2109G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693775 | ||||||
chr12:132693775
|
G | T | 12 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(9): Show | 19 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.237-2109G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693775 | ||||||
chr12:132693780
|
T | TA | 11 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2104_237-2103i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693780 | ||||||
chr12:132693791
|
T | TA | 6 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-2092dupA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693791 | |||||
chr12:132693792
|
AGTTAGCT others(41): Show |
A | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.237-2091_237-2044d others(50): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693792 | ||||||
chr12:132693795
|
T | G | 44 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(41): Show | 68 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.237-2089T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693795 | ||||||
chr12:132693799
|
T | G | 7 | a0001c0003t0003g0157a0001c0004t0002g0080a0001c0004t0004g0027others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.237-2085T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693799 | ||||||
chr12:132693808
|
CAGTT | C | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-2068_237-2065d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693808 | |||||
chr12:132693815
|
T | A | 2 | a0001c0003t0003g0157a0001c0004t0002g0080 | 2 | HG03195.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.237-2069T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693815 | ||||||
chr12:132693823
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.237-2061C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693823 | ||||||
chr12:132693824
|
T | G | 7 | a0001c0003t0003g0157a0001c0004t0002g0080a0001c0004t0004g0027others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.237-2060T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693824 | ||||||
chr12:132693824
|
T | TCCCTTAG others(64): Show |
7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2055_237-2054i others(73): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693824 | |||||
chr12:132693829
|
T | TA | 15 | a0001c0001t0001g0081a0001c0003t0003g0040a0001c0003t0003g0041others(12): Show | 18 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2055_237-2054i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693829 | ||||||
chr12:132693829
|
TGCC | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2054_237-2052d others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693829 | ||||||
chr12:132693831
|
C | T | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2053C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693831 | ||||||
chr12:132693835
|
T | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2049T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693835 | ||||||
chr12:132693836
|
T | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2048T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693836 | ||||||
chr12:132693836
|
T | TAGTTAGT others(13): Show |
12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2037_237-2036i others(22): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693836 | |||||
chr12:132693836
|
TAGTTAGT others(252): Show |
T | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.237-2036_237-1778d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693836 | |||||
chr12:132693848
|
T | G | 52 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(49): Show | 103 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.237-2036T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693848 | ||||||
chr12:132693848
|
TCCCTTGC others(87): Show |
T | 5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-1996_237-1903d others(96): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693848 | |||||
chr12:132693853
|
T | TA | 32 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(29): Show | 78 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-2031_237-2030i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693853 | ||||||
chr12:132693856
|
CAGTT | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2020_237-2017d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693856 | |||||
chr12:132693859
|
T | C | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-2025T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693859 | ||||||
chr12:132693860
|
T | C | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-2024T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693860 | ||||||
chr12:132693863
|
T | A | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.237-2021T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693863 | ||||||
chr12:132693872
|
T | G | 35 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(32): Show | 81 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.237-2012T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693872 | ||||||
chr12:132693877
|
TA | T | 7 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.237-2006delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693877 | ||||||
chr12:132693878
|
AGCCAGTT others(38): Show |
A | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-1996_237-1952d others(47): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693878 | |||||
chr12:132693880
|
C | T | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-2004C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693880 | ||||||
chr12:132693884
|
TTAGA | T | 7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1996_237-1993d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693884 | |||||
chr12:132693888
|
A | T | 31 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(28): Show | 45 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.237-1996A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693888 | ||||||
chr12:132693897
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.237-1987G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693897 | ||||||
chr12:132693897
|
G | T | 12 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(9): Show | 18 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.237-1987G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693897 | ||||||
chr12:132693902
|
T | TGCC | 13 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(10): Show | 16 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-1982_237-1981i others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693902 | ||||||
chr12:132693902
|
TA | T | 13 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(10): Show | 20 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.237-1981delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693902 | ||||||
chr12:132693905
|
C | T | 18 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(15): Show | 25 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.237-1979C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693905 | ||||||
chr12:132693906
|
C | CAGTT | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.237-1974_237-1971d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693906 | |||||
chr12:132693906
|
C | T | 20 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.237-1978C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693906 | ||||||
chr12:132693906
|
CAGTTAGT others(17): Show |
C | 1 | a0001c0001t0001g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.237-1942_237-1919d others(26): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693906 | |||||
chr12:132693913
|
T | A | 7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1971T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693913 | ||||||
chr12:132693918
|
G | T | 7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1966G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693918 | ||||||
chr12:132693942
|
G | A | 32 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(29): Show | 78 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-1942G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693942 | ||||||
chr12:132693942
|
G | T | 9 | a0001c0001t0001g0081a0001c0003t0003g0042a0001c0003t0003g0043others(6): Show | 11 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.237-1942G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693942 | ||||||
chr12:132693946
|
TTGCCAGT others(37): Show |
T | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1936_237-1893d others(46): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693946 | |||||
chr12:132693947
|
T | TA | 8 | a0001c0001t0001g0081a0001c0003t0003g0042a0001c0003t0003g0043others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1937_237-1936i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693947 | ||||||
chr12:132693953
|
T | C | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1931T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693953 | ||||||
chr12:132693954
|
T | C | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1930T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693954 | ||||||
chr12:132693954
|
TAGTTAGT others(14): Show |
T | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.237-1912_237-1892d others(23): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693954 | |||||
chr12:132693966
|
T | G | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1918T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693966 | ||||||
chr12:132693974
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-1910C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693974 | ||||||
chr12:132693975
|
C | CAGTT | 53 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(50): Show | 109 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.237-1905_237-1902d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693975 | |||||
chr12:132693975
|
C | T | 2 | a0001c0001t0001g0081a0001c0003t0003g0158 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.237-1909C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693975 | ||||||
chr12:132693982
|
T | A | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1902T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693982 | ||||||
chr12:132693983
|
G | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1901G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693983 | ||||||
chr12:132693987
|
T | G | 12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-1897T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693987 | ||||||
chr12:132693992
|
T | A | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1892T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693992 | ||||||
chr12:132693992
|
TGCC | T | 6 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1891_237-1889d others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693992 | ||||||
chr12:132693994
|
C | CCAGTTAG others(42): Show |
7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1868_237-1867i others(51): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132693994 | |||||
chr12:132693998
|
T | C | 6 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1886T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693998 | ||||||
chr12:132693999
|
T | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1885T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132693999 | ||||||
chr12:132694002
|
T | A | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1882T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694002 | ||||||
chr12:132694006
|
T | A | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-1878T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694006 | ||||||
chr12:132694011
|
T | G | 13 | a0001c0001t0001g0081a0001c0003t0003g0040a0001c0003t0003g0041others(10): Show | 16 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.237-1873T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694011 | ||||||
chr12:132694016
|
TA | T | 14 | a0001c0001t0001g0081a0001c0003t0003g0040a0001c0003t0003g0041others(11): Show | 17 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-1867delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694016 | ||||||
chr12:132694017
|
A | AGCCAGTT others(88): Show |
1 | a0001c0001t0001g0109 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.237-1830_237-1736d others(97): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694017 | |||||
chr12:132694017
|
A | AGCCAGTT others(38): Show |
1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1849_237-1848i others(47): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694017 | |||||
chr12:132694024
|
TAGTTAGT others(64): Show |
T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1830_237-1760d others(73): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694024 | |||||
chr12:132694036
|
G | T | 2 | a0001c0003t0003g0157a0001c0003t0003g0158 | 2 | HG00639.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.237-1848G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694036 | ||||||
chr12:132694041
|
T | TA | 32 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(29): Show | 78 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-1843_237-1842i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694041 | ||||||
chr12:132694051
|
T | A | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-1833T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694051 | ||||||
chr12:132694052
|
TA | T | 25 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(22): Show | 35 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.237-1830delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694052 | |||||
chr12:132694061
|
G | T | 14 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(11): Show | 17 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1823G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694061 | ||||||
chr12:132694069
|
C | T | 2 | a0001c0003t0003g0157a0001c0003t0003g0158 | 2 | HG00639.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.237-1815C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694069 | ||||||
chr12:132694073
|
TTAGA | T | 11 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-1807_237-1804d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694073 | |||||
chr12:132694077
|
A | T | 14 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(11): Show | 17 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1807A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694077 | ||||||
chr12:132694086
|
G | T | 13 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(10): Show | 16 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-1798G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694086 | ||||||
chr12:132694092
|
AGCCAGTT others(13): Show |
A | 2 | a0001c0002t0002g0002a0001c0002t0002g0022 | 2 | HG02004.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.237-1781_237-1762d others(22): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694092 | |||||
chr12:132694094
|
C | T | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1790C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694094 | ||||||
chr12:132694095
|
C | CAGTT | 13 | a0001c0001t0001g0081a0001c0002t0002g0006a0001c0002t0002g0009others(10): Show | 20 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.237-1785_237-1782d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694095 | |||||
chr12:132694095
|
C | CAGTTAGT others(18): Show |
7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1772_237-1771i others(27): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694095 | |||||
chr12:132694095
|
C | CAGTTAGT others(43): Show |
12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-1782_237-1781i others(52): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694095 | |||||
chr12:132694095
|
C | T | 2 | a0001c0005t0005g0070a0001c0005t0005g0071 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1789C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694095 | ||||||
chr12:132694101
|
GTGAGCGC others(402): Show |
G | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 75 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.237-1781_237-1373d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694101 | |||||
chr12:132694119
|
T | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1765T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694119 | ||||||
chr12:132694131
|
G | A | 3 | a0001c0001t0001g0100a0001c0005t0005g0070a0001c0005t0005g0071 | 3 | HG01074.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1753G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694131 | ||||||
chr12:132694143
|
T | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1741T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694143 | ||||||
chr12:132694146
|
T | A | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1738T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694146 | ||||||
chr12:132694146
|
TTAGTGAG others(383): Show |
T | 2 | a0001c0002t0002g0002a0001c0002t0002g0022 | 2 | HG02004.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.237-1729_237-1340d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694146 | |||||
chr12:132694155
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1729T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694155 | ||||||
chr12:132694160
|
T | G | 7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1724T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694160 | ||||||
chr12:132694167
|
TTAGTGAG others(10): Show |
T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1712_237-1696d others(19): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694167 | |||||
chr12:132694176
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1708T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694176 | ||||||
chr12:132694181
|
T | TGCC | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1703_237-1702i others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694181 | ||||||
chr12:132694184
|
C | T | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1700C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694184 | ||||||
chr12:132694192
|
A | T | 14 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(11): Show | 20 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.237-1692A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694192 | ||||||
chr12:132694197
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1687T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694197 | ||||||
chr12:132694213
|
T | TA | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1670dupA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694213 | |||||
chr12:132694221
|
T | G | 6 | a0001c0003t0003g0158a0001c0004t0004g0027a0001c0004t0004g0028others(3): Show | 10 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1663T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694221 | ||||||
chr12:132694229
|
C | T | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1655C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694229 | ||||||
chr12:132694237
|
T | A | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1647T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694237 | ||||||
chr12:132694246
|
T | G | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1638T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694246 | ||||||
chr12:132694251
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1633T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694251 | ||||||
chr12:132694255
|
C | CAGTT | 7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1625_237-1622d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694255 | |||||
chr12:132694259
|
TAGTGAGC others(102): Show |
T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1621_237-1513d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694259 | |||||
chr12:132694267
|
T | G | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1617T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694267 | ||||||
chr12:132694272
|
T | TA | 7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1612_237-1611i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694272 | ||||||
chr12:132694291
|
T | G | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1593T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694291 | ||||||
chr12:132694323
|
T | C | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1561T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694323 | ||||||
chr12:132694328
|
TAGTTAGT others(13): Show |
T | 1 | a0001c0010t0001g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.237-1508_237-1489d others(22): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694328 | |||||
chr12:132694340
|
G | T | 20 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.237-1544G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694340 | ||||||
chr12:132694345
|
T | TA | 13 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(10): Show | 16 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-1539_237-1538i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694345 | ||||||
chr12:132694348
|
C | CAGTTAGT others(403): Show |
1 | a0001c0003t0003g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.237-1529_237-1528i others(412): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694348 | |||||
chr12:132694348
|
C | CAGTTAGT others(407): Show |
10 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(7): Show | 13 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.237-1529_237-1528i others(416): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694348 | |||||
chr12:132694348
|
C | CAGTTAGT others(408): Show |
1 | a0001c0003t0003g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.237-1529_237-1528i others(417): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694348 | |||||
chr12:132694348
|
C | CAGTTAGT others(46): Show |
7 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(4): Show | 9 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1529_237-1528i others(55): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694348 | |||||
chr12:132694352
|
TAGTGAGC others(9): Show |
T | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-1528_237-1513d others(18): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694352 | |||||
chr12:132694368
|
C | CAGTT | 13 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(10): Show | 20 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.237-1512_237-1509d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694368 | |||||
chr12:132694368
|
C | CAGTTAGT others(46): Show |
1 | a0001c0003t0003g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237-1509_237-1508i others(55): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694368 | |||||
chr12:132694372
|
TAGTGAGC others(33): Show |
T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-1508_237-1469d others(42): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694372 | |||||
chr12:132694380
|
G | A | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-1504G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694380 | ||||||
chr12:132694380
|
G | T | 11 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(8): Show | 18 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-1504G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694380 | ||||||
chr12:132694385
|
T | TA | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1499_237-1498i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694385 | ||||||
chr12:132694392
|
T | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1492T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694392 | ||||||
chr12:132694392
|
TAGTTAGT others(13): Show |
T | 2 | a0001c0002t0002g0075a0001c0005t0005g0071 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.237-1480_237-1461d others(22): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694392 | |||||
chr12:132694392
|
TAGTTAGT others(59): Show |
T | 2 | a0001c0004t0002g0080a0001c0005t0005g0070 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.237-1480_237-1415d others(68): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694392 | |||||
chr12:132694404
|
G | T | 9 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(6): Show | 16 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-1480G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694404 | ||||||
chr12:132694412
|
C | CAGTT | 35 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 55 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.237-1468_237-1465d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694412 | |||||
chr12:132694415
|
TTAGTGAG others(35): Show |
T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1468_237-1427d others(44): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694415 | ||||||
chr12:132694419
|
TGAGCTCC others(59): Show |
T | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-1464_237-1399d others(68): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694419 | ||||||
chr12:132694424
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-1460T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694424 | ||||||
chr12:132694449
|
T | G | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1435T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694449 | ||||||
chr12:132694454
|
T | TGCC | 22 | a0001c0001t0001g0081a0001c0003t0003g0040a0001c0003t0003g0041others(19): Show | 27 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.237-1430_237-1429i others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694454 | ||||||
chr12:132694454
|
TA | T | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1429delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694454 | ||||||
chr12:132694457
|
C | T | 22 | a0001c0001t0001g0081a0001c0003t0003g0040a0001c0003t0003g0041others(19): Show | 27 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.237-1427C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694457 | ||||||
chr12:132694458
|
C | T | 22 | a0001c0001t0001g0081a0001c0003t0003g0040a0001c0003t0003g0041others(19): Show | 27 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.237-1426C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694458 | ||||||
chr12:132694462
|
T | TAGTTA | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1419_237-1418i others(7): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694462 | |||||
chr12:132694470
|
T | A | 20 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.237-1414T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694470 | ||||||
chr12:132694470
|
T | G | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1414T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694470 | ||||||
chr12:132694475
|
TA | T | 20 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(17): Show | 25 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.237-1408delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694475 | ||||||
chr12:132694486
|
T | A | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1398T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694486 | ||||||
chr12:132694487
|
T | A | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-1397T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694487 | ||||||
chr12:132694495
|
G | T | 2 | a0001c0004t0002g0080a0001c0005t0005g0070 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.237-1389G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694495 | ||||||
chr12:132694500
|
T | TA | 11 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-1384_237-1383i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694500 | ||||||
chr12:132694507
|
TAGTTA | T | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-1373_237-1369d others(7): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694507 | |||||
chr12:132694510
|
T | A | 1 | a0001c0003t0003g0157 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.237-1374T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694510 | ||||||
chr12:132694511
|
TA | T | 3 | a0001c0003t0003g0157a0001c0004t0002g0080a0001c0005t0005g0070 | 3 | HG03139.hp1 HG03195.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.237-1371delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694511 | |||||
chr12:132694512
|
A | T | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 75 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.237-1372A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694512 | ||||||
chr12:132694520
|
G | T | 2 | a0001c0004t0002g0080a0001c0005t0005g0070 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.237-1364G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694520 | ||||||
chr12:132694520
|
GCCCTTAG others(132): Show |
G | 1 | a0001c0005t0005g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.237-1348_237-1210d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694520 | |||||
chr12:132694525
|
TA | T | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 75 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.237-1358delA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694525 | ||||||
chr12:132694526
|
AGCCAGTT others(266): Show |
A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-1348_237-1076d others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694526 | |||||
chr12:132694536
|
A | T | 44 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(41): Show | 95 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.237-1348A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694536 | ||||||
chr12:132694545
|
G | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1339G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694545 | ||||||
chr12:132694550
|
T | TA | 6 | a0001c0003t0003g0157a0001c0004t0004g0027a0001c0004t0004g0028others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1334_237-1333i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694550 | ||||||
chr12:132694550
|
T | TAGCCACT others(19): Show |
8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-1334_237-1333i others(28): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694550 | ||||||
chr12:132694550
|
T | TAGCCAGT others(19): Show |
12 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-1334_237-1333i others(28): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694550 | ||||||
chr12:132694553
|
CAGTT | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG02572.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-1323_237-1320d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694553 | |||||
chr12:132694562
|
AGTGAGCG others(82): Show |
A | 2 | a0001c0004t0002g0080a0001c0005t0005g0070 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.237-1321_237-1233d others(91): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694562 | ||||||
chr12:132694569
|
G | A | 22 | a0001c0001t0001g0110a0001c0003t0003g0040a0001c0003t0003g0041others(19): Show | 27 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.237-1315G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694569 | ||||||
chr12:132694598
|
T | TGCC | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1286_237-1285i others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694598 | ||||||
chr12:132694601
|
C | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1283C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694601 | ||||||
chr12:132694602
|
C | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1282C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694602 | ||||||
chr12:132694622
|
C | CCAGT | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1262_237-1261i others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694622 | ||||||
chr12:132694630
|
A | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1254A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694630 | ||||||
chr12:132694635
|
T | G | 4 | a0001c0004t0004g0027a0001c0004t0004g0078a0001c0004t0004g0079others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-1249T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694635 | ||||||
chr12:132694640
|
TGCCAGTT others(18): Show |
T | 1 | a0001c0001t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.237-1208_237-1184d others(27): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694640 | |||||
chr12:132694651
|
T | TA | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1232dupA | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694651 | |||||
chr12:132694659
|
T | G | 7 | a0001c0004t0002g0080a0001c0004t0004g0027a0001c0004t0004g0028others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.237-1225T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694659 | ||||||
chr12:132694708
|
C | T | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.237-1176C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694708 | ||||||
chr12:132694732
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.237-1152C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694732 | ||||||
chr12:132694748
|
CTCCCTTA others(14): Show |
C | 1 | a0001c0002t0002g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.237-1135_237-1115d others(23): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694748 | ||||||
chr12:132694758
|
C | CAGTT | 67 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(64): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.237-1122_237-1119d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694758 | |||||
chr12:132694769
|
T | C | 69 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(66): Show | 131 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.237-1115T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694769 | ||||||
chr12:132694793
|
C | T | 1 | a0001c0002t0002g0077 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.237-1091C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694793 | ||||||
chr12:132694827
|
CAGTT | C | 3 | a0001c0001t0001g0133a0001c0002t0002g0006a0001c0002t0002g0009 | 10 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-1050_237-1047d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694827 | |||||
chr12:132694921
|
CAGTT | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0132others(1): Show | 5 | HG01255.hp2 HG01993.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-959_237-956del others(4): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694921 | |||||
chr12:132694921
|
CAGTTAGT others(42): Show |
C | 61 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(58): Show | 119 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.237-920_237-872del others(49): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132694921 | |||||
chr12:132694933
|
T | G | 1 | a0001c0002t0002g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.237-951T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694933 | ||||||
chr12:132694938
|
TAGCCAGT others(18): Show |
T | 1 | a0001c0002t0002g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.237-945_237-921del others(25): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694938 | ||||||
chr12:132694970
|
T | C | 1 | a0001c0002t0002g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.237-914T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132694970 | ||||||
chr12:132695031
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-853C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695031 | ||||||
chr12:132695032
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-852T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695032 | ||||||
chr12:132695038
|
AGCCAGTT others(17): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.237-828_237-805del others(24): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 132695038 | |||||
chr12:132695342
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.237-542G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695342 | ||||||
chr12:132695624
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.237-260C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695624 | ||||||
chr12:132695658
|
G | A | 1 | a0002c0007t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.237-226G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695658 | ||||||
chr12:132695663
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.237-221C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695663 | ||||||
chr12:132695740
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237-144G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695740 | ||||||
chr12:132695794
|
G | C | 70 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(67): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.237-90G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695794 | ||||||
chr12:132695815
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.237-69G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 2/4 | chr12 | 132695815 | ||||||
chr12:132696175
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.399+129T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696175 | ||||||
chr12:132696191
|
A | T | 1 | a0001c0002t0002g0024 | 2 | HG02056.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.399+145A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696191 | ||||||
chr12:132696669
|
A | G | 71 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(68): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.399+623A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696669 | ||||||
chr12:132696716
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0033 | 7 | HG01106.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+670C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696716 | ||||||
chr12:132696747
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.399+701C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696747 | ||||||
chr12:132696756
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.399+710C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696756 | ||||||
chr12:132696777
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.399+731G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696777 | ||||||
chr12:132696781
|
T | C | 1 | a0001c0005t0005g0070 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.399+735T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696781 | ||||||
chr12:132696867
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.399+821C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696867 | ||||||
chr12:132696955
|
A | G | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.399+909A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696955 | ||||||
chr12:132696971
|
C | T | 1 | a0001c0002t0002g0068 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.399+925C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132696971 | ||||||
chr12:132697131
|
A | G | 1 | a0001c0004t0002g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.399+1085A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697131 | ||||||
chr12:132697174
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.399+1128G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697174 | ||||||
chr12:132697271
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.399+1225C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697271 | ||||||
chr12:132697293
|
A | AAAAT | 61 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(58): Show | 119 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.399+1267_399+1270d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132697293 | |||||
chr12:132697393
|
T | TTTTA | 44 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(41): Show | 63 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.399+1367_399+1370d others(6): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132697393 | |||||
chr12:132697393
|
T | TTTTATTT others(1): Show |
33 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0002t0002g0002others(30): Show | 84 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.399+1363_399+1370d others(10): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132697393 | |||||
chr12:132697466
|
G | C | 1 | a0001c0002t0002g0058 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.399+1420G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697466 | ||||||
chr12:132697471
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.399+1425G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697471 | ||||||
chr12:132697500
|
C | T | 1 | a0001c0005t0005g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.399+1454C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697500 | ||||||
chr12:132697556
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.399+1510C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697556 | ||||||
chr12:132697559
|
T | C | 71 | a0001c0001t0001g0081a0001c0002t0002g0002a0001c0002t0002g0004others(68): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.399+1513T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697559 | ||||||
chr12:132697613
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.399+1567G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697613 | ||||||
chr12:132697693
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.399+1647A>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697693 | ||||||
chr12:132697727
|
A | G | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+1681A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697727 | ||||||
chr12:132697786
|
CAAG | C | 10 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(7): Show | 17 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.399+1744_399+1746d others(5): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132697786 | |||||
chr12:132697987
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.399+1941G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132697987 | ||||||
chr12:132698005
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.399+1959G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698005 | ||||||
chr12:132698009
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.399+1963C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698009 | ||||||
chr12:132698201
|
G | A | 1 | a0001c0002t0002g0023 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.399+2155G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698201 | ||||||
chr12:132698215
|
T | C | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+2169T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698215 | ||||||
chr12:132698267
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.399+2221C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698267 | ||||||
chr12:132698284
|
A | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0094others(1): Show | 6 | HG01891.hp2 HG01934.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+2238A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698284 | ||||||
chr12:132698289
|
T | C | 8 | a0001c0004t0002g0080a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.399+2243T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698289 | ||||||
chr12:132698313
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.399+2267C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698313 | ||||||
chr12:132698389
|
C | T | 8 | a0001c0004t0002g0080a0001c0004t0004g0027a0001c0004t0004g0028others(5): Show | 12 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.399+2343C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698389 | ||||||
chr12:132698458
|
C | T | 31 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(28): Show | 77 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+2412C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698458 | ||||||
chr12:132698464
|
T | C | 70 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(67): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.399+2418T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698464 | ||||||
chr12:132698664
|
T | C | 1 | a0001c0002t0002g0023 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.400-2586T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698664 | ||||||
chr12:132698771
|
C | T | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.400-2479C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132698771 | ||||||
chr12:132699123
|
C | T | 2 | a0001c0002t0002g0075a0001c0002t0002g0076 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.400-2127C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699123 | ||||||
chr12:132699332
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.400-1918A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699332 | ||||||
chr12:132699386
|
G | T | 1 | a0001c0002t0002g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.400-1864G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699386 | ||||||
chr12:132699388
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0082a0001c0001t0001g0099others(4): Show | 15 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.400-1862A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699388 | ||||||
chr12:132699526
|
C | CT | 17 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0036others(14): Show | 22 | HG01255.hp2 HG01361.hp1 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.400-1702dupT | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132699526 | |||||
chr12:132699526
|
C | CTT | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-1703_400-1702d others(4): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132699526 | |||||
chr12:132699526
|
CT | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.400-1702delT | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132699526 | |||||
chr12:132699526
|
CTT | C | 17 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0025others(14): Show | 50 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.400-1703_400-1702d others(4): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132699526 | |||||
chr12:132699623
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0033 | 7 | HG01106.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-1627C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699623 | ||||||
chr12:132699698
|
T | C | 62 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(59): Show | 120 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.400-1552T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699698 | ||||||
chr12:132699730
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0166 | 4 | HG00323.hp2 HG00741.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-1520C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699730 | ||||||
chr12:132699806
|
G | A | 2 | a0001c0002t0002g0006a0001c0002t0002g0009 | 9 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-1444G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699806 | ||||||
chr12:132699817
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.400-1433C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699817 | ||||||
chr12:132699833
|
C | T | 1 | a0001c0002t0002g0063 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.400-1417C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699833 | ||||||
chr12:132699884
|
G | A | 1 | a0001c0002t0002g0006 | 6 | HG01346.hp2 HG01358.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-1366G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132699884 | ||||||
chr12:132700040
|
AC | A | 3 | a0001c0002t0002g0055a0001c0002t0002g0064a0001c0003t0003g0149 | 3 | HG01884.hp2 HG03490.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.400-1208delC | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132700040 | |||||
chr12:132700041
|
C | CT | 5 | a0001c0002t0002g0058a0001c0002t0002g0077a0001c0002t0002g0162others(2): Show | 5 | HG03831.hp1 NA18977.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-1209_400-1208i others(3): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700041 | ||||||
chr12:132700042
|
C | T | 67 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(64): Show | 129 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.400-1208C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700042 | ||||||
chr12:132700111
|
G | A | 1 | a0001c0002t0002g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.400-1139G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700111 | ||||||
chr12:132700216
|
A | G | 2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.400-1034A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700216 | ||||||
chr12:132700334
|
A | G | 1 | a0001c0004t0004g0028 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.400-916A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700334 | ||||||
chr12:132700449
|
CAT | C | 2 | a0001c0002t0002g0006a0001c0002t0002g0009 | 9 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-798_400-797del others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132700449 | |||||
chr12:132700504
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.400-746C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700504 | ||||||
chr12:132700751
|
C | T | 1 | a0003c0009t0002g0062 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.400-499C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700751 | ||||||
chr12:132700752
|
G | A | 1 | a0004c0006t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400-498G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700752 | ||||||
chr12:132700848
|
C | CT | 67 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(64): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.400-387dupT | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132700848 | |||||
chr12:132700848
|
C | CTT | 6 | a0001c0002t0002g0077a0001c0002t0002g0162a0001c0004t0004g0028others(3): Show | 9 | HG01109.hp1 HG02717.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-388_400-387dup others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 132700848 | |||||
chr12:132700924
|
T | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.400-326T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700924 | ||||||
chr12:132700950
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.400-300T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132700950 | ||||||
chr12:132701115
|
CAT | C | 2 | a0001c0002t0002g0022a0001c0002t0002g0055 | 3 | HG00738.hp2 HG03490.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.400-134_400-133del others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132701115 | ||||||
chr12:132701130
|
C | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-120C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132701130 | ||||||
chr12:132701225
|
A | C | 1 | a0001c0002t0002g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.400-25A>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 3/4 | chr12 | 132701225 | ||||||
chr12:132701397
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(169): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.519+28T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701397 | ||||||
chr12:132701452
|
C | CT | 11 | a0001c0001t0001g0030a0001c0001t0001g0090a0001c0003t0003g0043others(8): Show | 14 | HG00280.hp1 HG00544.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.519+84dupT | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 132701452 | |||||
chr12:132701452
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.519+83C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701452 | ||||||
chr12:132701489
|
G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 269 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.519+120G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701489 | ||||||
chr12:132701500
|
G | A | 4 | a0001c0001t0001g0090a0001c0002t0002g0075a0001c0002t0002g0076others(1): Show | 6 | HG01109.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+131G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701500 | ||||||
chr12:132701518
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.519+149C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701518 | ||||||
chr12:132701623
|
T | G | 1 | a0001c0001t0001g0032 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.519+254T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701623 | ||||||
chr12:132701895
|
G | A | 1 | a0001c0004t0005g0010 | 3 | HG01109.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.519+526G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701895 | ||||||
chr12:132701895
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.519+526G>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701895 | ||||||
chr12:132701907
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0090 | 5 | HG02559.hp2 HG02965.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+538T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132701907 | ||||||
chr12:132702033
|
T | G | 7 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(4): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+664T>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702033 | ||||||
chr12:132702048
|
C | T | 62 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(59): Show | 120 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.519+679C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702048 | ||||||
chr12:132702172
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.519+803A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702172 | ||||||
chr12:132702182
|
C | A | 1 | a0004c0006t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.519+813C>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702182 | ||||||
chr12:132702212
|
G | A | 4 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(1): Show | 6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+843G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702212 | ||||||
chr12:132702392
|
AG | A | 1 | a0001c0001t0001g0007 | 5 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+1025delG | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 132702392 | |||||
chr12:132702517
|
G | A | 1 | a0001c0002t0002g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.519+1148G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702517 | ||||||
chr12:132702518
|
A | C | 11 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0048others(8): Show | 18 | HG00140.hp2 HG00733.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.519+1149A>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702518 | ||||||
chr12:132702521
|
C | T | 8 | a0001c0003t0003g0042a0001c0003t0003g0043a0001c0003t0003g0149others(5): Show | 10 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.519+1152C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702521 | ||||||
chr12:132702544
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.519+1175C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702544 | ||||||
chr12:132702557
|
C | T | 1 | a0001c0002t0002g0059 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.519+1188C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702557 | ||||||
chr12:132702848
|
G | A | 13 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0044others(10): Show | 16 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+1479G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702848 | ||||||
chr12:132702883
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(13): Show | 31 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(28): Show |
intron_variant | MODIFIER | c.519+1514G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702883 | ||||||
chr12:132702893
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0127 | 4 | HG02109.hp2 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1524G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702893 | ||||||
chr12:132702909
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.519+1540C>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702909 | ||||||
chr12:132702909
|
C | G | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.519+1540C>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132702909 | ||||||
chr12:132703033
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.520-1586C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703033 | ||||||
chr12:132703050
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.520-1569G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703050 | ||||||
chr12:132703078
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.520-1541A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703078 | ||||||
chr12:132703168
|
C | T | 1 | a0001c0002t0002g0023 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.520-1451C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703168 | ||||||
chr12:132703190
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.520-1429T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703190 | ||||||
chr12:132703280
|
T | A | 6 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0004g0078others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-1339T>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703280 | ||||||
chr12:132703318
|
G | A | 1 | a0001c0003t0003g0169 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.520-1301G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703318 | ||||||
chr12:132703398
|
A | T | 4 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0076others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-1221A>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703398 | ||||||
chr12:132703400
|
G | T | 5 | a0001c0004t0004g0027a0001c0004t0004g0028a0001c0004t0005g0010others(2): Show | 9 | HG01109.hp1 HG01243.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-1219G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703400 | ||||||
chr12:132703472
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0004t0004g0027others(5): Show | 17 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-1147A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703472 | ||||||
chr12:132703657
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0002t0002g0002others(69): Show | 139 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.520-962G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703657 | ||||||
chr12:132703690
|
A | G | 1 | a0001c0002t0002g0061 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.520-929A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703690 | ||||||
chr12:132703766
|
A | G | 52 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0022others(49): Show | 103 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.520-853A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703766 | ||||||
chr12:132703849
|
A | G | 1 | a0001c0002t0002g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.520-770A>G | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132703849 | ||||||
chr12:132703888
|
TGA | T | 21 | a0001c0003t0003g0040a0001c0003t0003g0041a0001c0003t0003g0042others(18): Show | 26 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.520-728_520-727del others(2): Show |
PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 132703888 | |||||
chr12:132704008
|
C | T | 1 | a0001c0001t0001g0020 | 3 | HG01884.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.520-611C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704008 | ||||||
chr12:132704077
|
C | T | 1 | a0001c0002t0002g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.520-542C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704077 | ||||||
chr12:132704124
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.520-495T>C | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704124 | ||||||
chr12:132704250
|
C | T | 1 | a0001c0002t0002g0066 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.520-369C>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704250 | ||||||
chr12:132704251
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.520-368G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704251 | ||||||
chr12:132704387
|
G | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01074.hp1 HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.520-232G>T | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704387 | ||||||
chr12:132704420
|
G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0004t0004g0027others(6): Show | 18 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.520-199G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704420 | ||||||
chr12:132704479
|
G | A | 1 | a0001c0001t0001g0013 | 3 | NA18983.hp1 NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.520-140G>A | PXMP2 | ENSG00000176894.10 | transcript | ENST00000317479.8 | protein_coding | 4/4 | chr12 | 132704479 |