Item | Value |
---|---|
geneid | 29899 |
ensemblid | ENSG00000121957.15 |
hgncid | 29501 |
symbol | GPSM2 |
name | G protein signaling modulator 2 |
refseq_nuc | NM_013296.5 |
refseq_prot | NP_037428.3 |
ensembl_nuc | ENST00000264126.9 |
ensembl_prot | ENSP00000264126.3 |
mane_status | MANE Select |
chr | chr1 |
start | 108876985 |
end | 108934545 |
strand | + |
ver | v1.2 |
region | chr1:108876985-108934545 |
region5000 | chr1:108871985-108939545 |
regionname0 | GPSM2_chr1_108876985_108934545 |
regionname5000 | GPSM2_chr1_108871985_108939545 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 684 | 154 | 25 | 31 | 73 | 6 | 17 | 53 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002 | 0/0 | 683 | 57 | 31 | 10 | 9 | 4 | 3 | 9 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0003 | 0/0 | 683 | 19 | 14 | 1 | 0 | 2 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004 | 0/0 | 683 | 18 | 6 | 0 | 4 | 0 | 8 | 4 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0005 | 0/0 | 684 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0006 | 0/0 | 683 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0007 | 0/0 | 684 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0008 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0009 | 0/0 | 683 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0010 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2055 | 153 | 25 | 31 | 73 | 6 | 16 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0002 | 0/0 | 2052 | 41 | 16 | 9 | 9 | 4 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0003 | 0/0 | 2052 | 19 | 14 | 1 | 0 | 2 | 2 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0004 | 0/0 | 2052 | 18 | 6 | 0 | 4 | 0 | 8 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0005 | 0/0 | 2052 | 10 | 9 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0006 | 0/0 | 2052 | 5 | 5 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0007 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0008 | 0/0 | 2052 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0009 | 0/0 | 2055 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0010 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0011 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0012 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0013 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
c0014 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 5098 | 82 | 21 | 19 | 29 | 3 | 9 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0002 | 0/0 | 5098 | 48 | 1 | 6 | 32 | 3 | 6 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0003 | 0/0 | 5098 | 13 | 12 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0004 | 0/0 | 5103 | 9 | 1 | 0 | 3 | 0 | 5 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0005 | 0/0 | 5243 | 9 | 5 | 4 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0006 | 0/0 | 4952 | 8 | 0 | 1 | 5 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0007 | 0/0 | 5098 | 6 | 6 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0008 | 0/0 | 5098 | 6 | 5 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0009 | 0/0 | 4952 | 5 | 3 | 0 | 0 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0010 | 0/0 | 4953 | 5 | 5 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0011 | 0/0 | 5099 | 4 | 0 | 2 | 0 | 0 | 2 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0012 | 0/0 | 5102 | 4 | 0 | 0 | 4 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0013 | 0/0 | 5103 | 4 | 0 | 0 | 1 | 0 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0014 | 0/0 | 5094 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0015 | 0/0 | 5098 | 3 | 0 | 3 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0016 | 0/0 | 5098 | 3 | 0 | 0 | 3 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0017 | 0/0 | 5099 | 3 | 0 | 0 | 2 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0018 | 0/0 | 5099 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0019 | 0/0 | 4952 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0020 | 0/0 | 5098 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0021 | 0/0 | 5098 | 3 | 0 | 0 | 0 | 2 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0022 | 0/0 | 5099 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0023 | 0/0 | 5098 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0024 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0025 | 0/0 | 4952 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0026 | 0/0 | 5099 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0027 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0028 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0029 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0030 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0031 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0032 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0033 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0034 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0035 | 0/1 | 5098 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0036 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0037 | 0/0 | 5099 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0038 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0039 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0040 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0041 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0042 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0043 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0044 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0045 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0046 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0047 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0048 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0049 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0050 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0051 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
t0052 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0007 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2055 | 153 | 25 | 31 | 73 | 6 | 16 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0014 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002 | 0/0 | 2052 | 41 | 16 | 9 | 9 | 4 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0005 | 0/0 | 2052 | 10 | 9 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0006 | 0/0 | 2052 | 5 | 5 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0010 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0003c0003 | 0/0 | 2052 | 19 | 14 | 1 | 0 | 2 | 2 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004c0004 | 0/0 | 2052 | 18 | 6 | 0 | 4 | 0 | 8 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0005c0007 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0006c0008 | 0/0 | 2052 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0007c0009 | 0/0 | 2055 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0008c0011 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0009c0013 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0010c0012 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7152 | 75 | 16 | 18 | 29 | 3 | 8 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0002 | 0/0 | 7152 | 47 | 1 | 6 | 31 | 3 | 6 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0007 | 0/0 | 7152 | 6 | 6 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0012 | 0/0 | 7156 | 4 | 0 | 0 | 4 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0015 | 0/0 | 7152 | 3 | 0 | 3 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0016 | 0/0 | 7152 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0023 | 0/0 | 7152 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0024 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0028 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0029 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0030 | 0/0 | 7152 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0035 | 0/1 | 7152 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0036 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0037 | 0/0 | 7153 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0038 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0039 | 0/0 | 7152 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0040 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0041 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0042 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0046 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0001t0052 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0001c0014t0001 | 0/0 | 7152 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0002 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0005 | 0/0 | 7294 | 9 | 5 | 4 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0006 | 0/0 | 7003 | 7 | 0 | 1 | 4 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0009 | 0/0 | 7003 | 5 | 3 | 0 | 0 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0011 | 0/0 | 7150 | 4 | 0 | 2 | 0 | 0 | 2 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0017 | 0/0 | 7150 | 3 | 0 | 0 | 2 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0018 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0019 | 0/0 | 7003 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0020 | 0/0 | 7149 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0025 | 0/0 | 7003 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0026 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0027 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0043 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0002t0045 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0005t0008 | 0/0 | 7149 | 6 | 5 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0005t0014 | 0/0 | 7145 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0005t0051 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0006t0010 | 0/0 | 7004 | 5 | 5 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0002c0010t0032 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0003c0003t0003 | 0/0 | 7149 | 13 | 12 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0003c0003t0021 | 0/0 | 7149 | 3 | 0 | 0 | 0 | 2 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0003c0003t0047 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0003c0003t0048 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0003c0003t0049 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004c0004t0004 | 0/0 | 7154 | 9 | 1 | 0 | 3 | 0 | 5 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004c0004t0013 | 0/0 | 7154 | 4 | 0 | 0 | 1 | 0 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004c0004t0022 | 0/0 | 7150 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004c0004t0031 | 0/0 | 7154 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004c0004t0033 | 0/0 | 7152 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0004c0004t0034 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0005c0007t0001 | 0/0 | 7152 | 4 | 4 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0006c0008t0018 | 0/0 | 7150 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0006c0008t0044 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0007c0009t0001 | 0/0 | 7152 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0008c0011t0006 | 0/0 | 7003 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0009c0013t0050 | 0/0 | 7016 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
a0010c0012t0016 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | copy fasta | chr1 | 108871985 | 108939545 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0012g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0012g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0012g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0015g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0015g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0015g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0016g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0016g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0023g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0024g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0028g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0029g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0030g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0035g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0036g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0037g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0038g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0039g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0040g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0041g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0042g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0046g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0001t0052g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0001c0014t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0005g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0005g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0005g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0006g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0006g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0009g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0009g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0011g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0011g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0011g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0017g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0017g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0017g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0019g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0019g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0019g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0020g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0025g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0026g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0027g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0043g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0002t0045g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0008g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0008g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0014g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0005t0051g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0006t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0006t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0006t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0006t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0002c0010t0032g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0021g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0021g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0021g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0047g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0048g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0003c0003t0049g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0013g0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0013g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0022g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0022g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0031g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0033g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0004c0004t0034g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0005c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0005c0007t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0005c0007t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0005c0007t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0006c0008t0018g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0006c0008t0018g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0006c0008t0044g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0007c0009t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0007c0009t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0008c0011t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0009c0013t0050g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
a0010c0012t0016g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00140 | hp1 | a0003 | c0003 | t0021 | g0227 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00280 | hp2 | a0003 | c0003 | t0021 | g0228 | EUR | FIN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00408 | hp2 | a0001 | c0001 | t0012 | g0176 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG00741 | hp2 | a0001 | c0001 | t0029 | g0179 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01071 | hp1 | a0007 | c0009 | t0001 | g0166 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01071 | hp2 | a0001 | c0001 | t0037 | g0159 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01081 | hp1 | a0001 | c0001 | t0042 | g0158 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01099 | hp1 | a0002 | c0002 | t0019 | g0035 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01099 | hp2 | a0002 | c0002 | t0011 | g0044 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01109 | hp1 | a0006 | c0008 | t0018 | g0018 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01109 | hp2 | a0001 | c0001 | t0015 | g0086 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01167 | hp2 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01169 | hp1 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01175 | hp1 | a0002 | c0002 | t0011 | g0048 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01243 | hp1 | a0001 | c0001 | t0038 | g0167 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01243 | hp2 | a0003 | c0003 | t0003 | g0230 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01346 | hp2 | a0002 | c0002 | t0025 | g0002 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01433 | hp2 | a0002 | c0005 | t0008 | g0059 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01515 | hp2 | a0002 | c0002 | t0006 | g0028 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01516 | hp1 | a0002 | c0002 | t0009 | g0038 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0116 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01517 | hp1 | a0002 | c0002 | t0006 | g0023 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01517 | hp2 | a0002 | c0002 | t0009 | g0036 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01884 | hp1 | a0002 | c0002 | t0043 | g0047 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01884 | hp2 | a0002 | c0006 | t0010 | g0004 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01891 | hp2 | a0003 | c0003 | t0003 | g0232 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01952 | hp1 | a0002 | c0002 | t0005 | g0014 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01952 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01981 | hp1 | a0001 | c0001 | t0015 | g0085 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02027 | hp1 | a0001 | c0001 | t0024 | g0090 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02040 | hp2 | a0001 | c0001 | t0046 | g0068 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02055 | hp1 | a0002 | c0010 | t0032 | g0205 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02132 | hp1 | a0001 | c0001 | t0041 | g0191 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02132 | hp2 | a0001 | c0001 | t0028 | g0108 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02145 | hp1 | a0002 | c0005 | t0014 | g0062 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02257 | hp2 | a0003 | c0003 | t0003 | g0243 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02258 | hp1 | a0002 | c0002 | t0005 | g0203 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02258 | hp2 | a0002 | c0005 | t0051 | g0057 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02300 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02451 | hp1 | a0003 | c0003 | t0047 | g0234 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02572 | hp1 | a0003 | c0003 | t0003 | g0244 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02572 | hp2 | a0002 | c0002 | t0020 | g0039 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02615 | hp2 | a0004 | c0004 | t0034 | g0032 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02622 | hp2 | a0005 | c0007 | t0001 | g0139 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02630 | hp2 | a0002 | c0005 | t0008 | g0005 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02647 | hp1 | a0003 | c0003 | t0003 | g0237 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02647 | hp2 | a0002 | c0006 | t0010 | g0043 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02698 | hp2 | a0002 | c0002 | t0011 | g0045 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02717 | hp2 | a0006 | c0008 | t0044 | g0017 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02723 | hp1 | a0001 | c0001 | t0023 | g0049 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02723 | hp2 | a0002 | c0005 | t0008 | g0055 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02735 | hp1 | a0002 | c0002 | t0011 | g0046 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02738 | hp2 | a0003 | c0003 | t0021 | g0229 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02809 | hp1 | a0003 | c0003 | t0003 | g0233 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02809 | hp2 | a0005 | c0007 | t0001 | g0220 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02818 | hp1 | a0002 | c0006 | t0010 | g0021 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02818 | hp2 | a0002 | c0002 | t0005 | g0202 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02886 | hp1 | a0004 | c0004 | t0031 | g0201 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02886 | hp2 | a0002 | c0002 | t0020 | g0003 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02895 | hp1 | a0002 | c0002 | t0009 | g0041 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02895 | hp2 | a0003 | c0003 | t0003 | g0239 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02897 | hp1 | a0002 | c0002 | t0009 | g0040 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02897 | hp2 | a0002 | c0005 | t0008 | g0058 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02922 | hp1 | a0005 | c0007 | t0001 | g0221 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02922 | hp2 | a0002 | c0005 | t0008 | g0005 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02965 | hp1 | a0002 | c0002 | t0019 | g0034 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02965 | hp2 | a0005 | c0007 | t0001 | g0223 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02970 | hp1 | a0004 | c0004 | t0004 | g0200 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02970 | hp2 | a0002 | c0002 | t0020 | g0003 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02976 | hp2 | a0002 | c0006 | t0010 | g0004 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03041 | hp1 | a0004 | c0004 | t0033 | g0042 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03041 | hp2 | a0002 | c0002 | t0005 | g0013 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03098 | hp1 | a0003 | c0003 | t0003 | g0240 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03098 | hp2 | a0009 | c0013 | t0050 | g0056 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03130 | hp2 | a0003 | c0003 | t0003 | g0245 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03139 | hp2 | a0002 | c0002 | t0045 | g0019 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03195 | hp1 | a0006 | c0008 | t0018 | g0218 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03209 | hp1 | a0002 | c0002 | t0005 | g0013 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03209 | hp2 | a0001 | c0001 | t0023 | g0050 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03239 | hp1 | a0001 | c0014 | t0001 | g0132 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03239 | hp2 | a0001 | c0001 | t0030 | g0136 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03453 | hp2 | a0002 | c0006 | t0010 | g0020 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0242 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03490 | hp2 | a0004 | c0004 | t0013 | g0001 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03491 | hp2 | a0004 | c0004 | t0004 | g0199 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03492 | hp1 | a0004 | c0004 | t0004 | g0197 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03492 | hp2 | a0004 | c0004 | t0013 | g0001 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03540 | hp1 | a0002 | c0002 | t0019 | g0037 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03540 | hp2 | a0002 | c0002 | t0018 | g0016 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03579 | hp1 | a0004 | c0004 | t0022 | g0063 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03579 | hp2 | a0002 | c0005 | t0008 | g0054 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03654 | hp1 | a0004 | c0004 | t0004 | g0195 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03704 | hp1 | a0004 | c0004 | t0013 | g0001 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG04115 | hp1 | a0003 | c0003 | t0049 | g0231 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG04115 | hp2 | a0004 | c0004 | t0004 | g0198 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG04228 | hp1 | a0002 | c0002 | t0017 | g0026 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG04228 | hp2 | a0001 | c0001 | t0039 | g0065 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18522 | hp2 | a0003 | c0003 | t0003 | g0241 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18906 | hp1 | a0003 | c0003 | t0003 | g0236 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18906 | hp2 | a0002 | c0005 | t0014 | g0061 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18944 | hp1 | a0004 | c0004 | t0004 | g0194 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18945 | hp2 | a0001 | c0001 | t0052 | g0100 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18948 | hp1 | a0008 | c0011 | t0006 | g0025 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18959 | hp1 | a0001 | c0001 | t0016 | g0214 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18959 | hp2 | a0001 | c0001 | t0012 | g0152 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18965 | hp1 | a0002 | c0002 | t0006 | g0051 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18968 | hp2 | a0002 | c0002 | t0006 | g0052 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18969 | hp2 | a0004 | c0004 | t0004 | g0196 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18970 | hp2 | a0002 | c0002 | t0017 | g0022 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18972 | hp1 | a0001 | c0001 | t0016 | g0175 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18983 | hp2 | a0002 | c0002 | t0026 | g0030 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18990 | hp1 | a0004 | c0004 | t0004 | g0011 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA18990 | hp2 | a0001 | c0001 | t0012 | g0010 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19000 | hp2 | a0010 | c0012 | t0016 | g0169 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19001 | hp1 | a0002 | c0002 | t0006 | g0031 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19003 | hp2 | a0001 | c0001 | t0036 | g0174 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19005 | hp2 | a0001 | c0001 | t0012 | g0181 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19030 | hp1 | a0003 | c0003 | t0048 | g0235 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0144 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19043 | hp2 | a0004 | c0004 | t0022 | g0064 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19066 | hp2 | a0004 | c0004 | t0013 | g0011 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19075 | hp1 | a0002 | c0002 | t0027 | g0027 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19080 | hp2 | a0001 | c0001 | t0040 | g0097 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19084 | hp2 | a0002 | c0002 | t0017 | g0029 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19085 | hp1 | a0002 | c0002 | t0006 | g0053 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ASW | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA20129 | hp2 | a0002 | c0002 | t0005 | g0204 | AFR | ASW | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
NA20905 | hp2 | a0004 | c0004 | t0004 | g0193 | SAS | GIH | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG01123 | hp2 | a0002 | c0002 | t0005 | g0014 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02109 | hp2 | a0002 | c0005 | t0014 | g0060 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02486 | hp2 | a0002 | c0002 | t0009 | g0033 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02559 | hp1 | a0007 | c0009 | t0001 | g0157 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG02559 | hp2 | a0003 | c0003 | t0003 | g0238 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0035 | g0007 | REF | REF | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0225 | REF | REF | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:108897593
|
G | A | 2 | a0003a0005 | 23 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(20): Show |
missense_variant | MODERATE | c.380G>A | p.Arg127Gln | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 4/15 | 872/7152 | 380/2055 | 127/684 | chr1 | 108897593 | ||
chr1:108901810
|
G | A | 1 | a0008 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.818G>A | p.Arg273Gln | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/15 | 1310/7152 | 818/2055 | 273/684 | chr1 | 108901810 | ||
chr1:108904128
|
G | A | 1 | a0007 | 2 | HG01071.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.1066G>A | p.Gly356Arg | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/15 | 1558/7152 | 1066/2055 | 356/684 | chr1 | 108904128 | ||
chr1:108914392
|
A | G | 1 | a0010 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.1247A>G | p.Lys416Arg | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/15 | 1739/7152 | 1247/2055 | 416/684 | chr1 | 108914392 | ||
chr1:108918719
|
C | T | 2 | a0004a0009 | 19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
missense_variant | MODERATE | c.1370C>T | p.Thr457Met | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/15 | 1862/7152 | 1370/2055 | 457/684 | chr1 | 108918719 | ||
chr1:108922543
|
ACTT | A | 6 | a0002a0003a0004others(3): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
disruptive_inframe_deletion | MODERATE | c.1572_1574delTTC | p.Ser525del | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/15 | 2064/7152 | 1572/2055 | 524/684 | INFO_REALIGN_3_PRIME | chr1 | 108922543 | |
chr1:108924138
|
C | T | 1 | a0009 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1739C>T | p.Ser580Leu | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/15 | 2231/7152 | 1739/2055 | 580/684 | chr1 | 108924138 | ||
chr1:108929705
|
C | T | 1 | a0006 | 3 | HG01109.hp1 HG02717.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.1820C>T | p.Ser607Phe | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2312/7152 | 1820/2055 | 607/684 | chr1 | 108929705 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:108896894
|
G | A | 1 | a0002c0010 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.87G>A | p.Leu29Leu | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/15 | 579/7152 | 87/2055 | 29/684 | chr1 | 108896894 | ||
chr1:108896993
|
C | T | 1 | a0001c0014 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.186C>T | p.Ser62Ser | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/15 | 678/7152 | 186/2055 | 62/684 | chr1 | 108896993 | ||
chr1:108898950
|
A | G | 2 | a0002c0005a0009c0013 | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
synonymous_variant | LOW | c.753A>G | p.Ala251Ala | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/15 | 1245/7152 | 753/2055 | 251/684 | chr1 | 108898950 | ||
chr1:108901820
|
A | G | 1 | a0002c0006 | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
synonymous_variant | LOW | c.828A>G | p.Lys276Lys | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/15 | 1320/7152 | 828/2055 | 276/684 | chr1 | 108901820 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:108876991
|
G | C | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-486G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | 8532 | chr1 | 108876991 | |||||
chr1:108877008
|
C | G | 1 | a0001c0001t0052 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-469C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | 8515 | chr1 | 108877008 | |||||
chr1:108877048
|
C | T | 4 | a0002c0005t0008a0002c0005t0014a0002c0005t0051others(1): Show | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-429C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | chr1 | 108877048 | ||||||
chr1:108877219
|
C | T | 5 | a0003c0003t0003a0003c0003t0021a0003c0003t0047others(2): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-258C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | 8304 | chr1 | 108877219 | |||||
chr1:108885293
|
G | A | 1 | a0001c0001t0024 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-230G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/15 | 230 | chr1 | 108885293 | |||||
chr1:108885409
|
C | T | 1 | a0001c0001t0046 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/15 | 114 | chr1 | 108885409 | |||||
chr1:108930151
|
G | A | 30 | a0001c0001t0002a0001c0001t0015a0001c0001t0016others(27): Show | 119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*211G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 211 | chr1 | 108930151 | |||||
chr1:108930191
|
T | C | 14 | a0001c0001t0002a0001c0001t0015a0001c0001t0016others(11): Show | 64 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*251T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 251 | chr1 | 108930191 | |||||
chr1:108930291
|
C | T | 1 | a0002c0005t0051 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 351 | chr1 | 108930291 | |||||
chr1:108930299
|
T | G | 6 | a0002c0002t0006a0002c0002t0017a0002c0002t0025others(3): Show | 14 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*359T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 359 | chr1 | 108930299 | |||||
chr1:108930395
|
C | T | 20 | a0002c0002t0005a0002c0002t0009a0002c0002t0011others(17): Show | 61 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*455C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 455 | chr1 | 108930395 | |||||
chr1:108930407
|
G | T | 1 | a0003c0003t0048 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 467 | chr1 | 108930407 | |||||
chr1:108930432
|
G | T | 1 | a0002c0006t0010 | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 492 | chr1 | 108930432 | |||||
chr1:108930496
|
TCCTGTAA others(124): Show |
T | 1 | a0009c0013t0050 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*573_*703del | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 573 | INFO_REALIGN_3_PRIME | chr1 | 108930496 | ||||
chr1:108930538
|
G | A | 1 | a0001c0001t0035 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*598G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 598 | chr1 | 108930538 | |||||
chr1:108930614
|
C | A | 1 | a0001c0001t0028 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 674 | chr1 | 108930614 | |||||
chr1:108930654
|
C | T | 1 | a0004c0004t0033 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 714 | chr1 | 108930654 | |||||
chr1:108930664
|
G | A | 1 | a0001c0001t0036 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*724G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 724 | chr1 | 108930664 | |||||
chr1:108930696
|
C | G | 1 | a0009c0013t0050 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 756 | chr1 | 108930696 | |||||
chr1:108930808
|
G | A | 1 | a0001c0001t0029 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 868 | chr1 | 108930808 | |||||
chr1:108930890
|
CAA | C | 31 | a0002c0002t0005a0002c0002t0006a0002c0002t0009others(28): Show | 94 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*963_*964delAA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 963 | INFO_REALIGN_3_PRIME | chr1 | 108930890 | ||||
chr1:108930905
|
C | T | 33 | a0002c0002t0005a0002c0002t0006a0002c0002t0009others(30): Show | 98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*965C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 965 | chr1 | 108930905 | |||||
chr1:108930983
|
T | C | 7 | a0002c0002t0006a0002c0002t0025a0004c0004t0004others(4): Show | 24 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1043T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1043 | chr1 | 108930983 | |||||
chr1:108930991
|
G | A | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1051G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1051 | chr1 | 108930991 | |||||
chr1:108931019
|
TC | T | 1 | a0002c0002t0005 | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1081delC | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1081 | INFO_REALIGN_3_PRIME | chr1 | 108931019 | ||||
chr1:108931104
|
A | C | 1 | a0002c0010t0032 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1164 | chr1 | 108931104 | |||||
chr1:108931184
|
G | A | 1 | a0001c0001t0015 | 3 | HG01109.hp2 HG01952.hp2 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1244G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1244 | chr1 | 108931184 | |||||
chr1:108931204
|
G | A | 33 | a0002c0002t0005a0002c0002t0006a0002c0002t0009others(30): Show | 98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1264G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1264 | chr1 | 108931204 | |||||
chr1:108931211
|
TAAAC | T | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1277_*1280delAACA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1277 | INFO_REALIGN_3_PRIME | chr1 | 108931211 | ||||
chr1:108931316
|
T | C | 1 | a0003c0003t0047 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1376 | chr1 | 108931316 | |||||
chr1:108931399
|
AG | A | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1460delG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1460 | chr1 | 108931399 | |||||
chr1:108931400
|
G | A | 1 | a0004c0004t0031 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1460 | chr1 | 108931400 | |||||
chr1:108931599
|
C | T | 33 | a0002c0002t0005a0002c0002t0006a0002c0002t0009others(30): Show | 98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1659C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1659 | chr1 | 108931599 | |||||
chr1:108931628
|
T | TA | 3 | a0001c0001t0037a0002c0002t0027a0002c0005t0014 | 5 | HG01071.hp2 HG02109.hp2 HG02145.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1703dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1704 | INFO_REALIGN_3_PRIME | chr1 | 108931628 | ||||
chr1:108931628
|
T | TAA | 26 | a0002c0002t0005a0002c0002t0006a0002c0002t0009others(23): Show | 74 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1702_*1703dupAA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1704 | INFO_REALIGN_3_PRIME | chr1 | 108931628 | ||||
chr1:108931628
|
T | TAAA | 4 | a0002c0006t0010a0004c0004t0004a0004c0004t0013others(1): Show | 19 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1701_*1703dupAAA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1704 | INFO_REALIGN_3_PRIME | chr1 | 108931628 | ||||
chr1:108931679
|
T | C | 2 | a0002c0002t0009a0002c0002t0019 | 8 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1739T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1739 | chr1 | 108931679 | |||||
chr1:108931725
|
G | GGTAA | 1 | a0001c0001t0012 | 4 | HG00408.hp2 NA18959.hp2 NA18990.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1788_*1791dupAAGT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1792 | INFO_REALIGN_3_PRIME | chr1 | 108931725 | ||||
chr1:108931959
|
T | C | 1 | a0001c0001t0007 | 6 | HG02055.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2019T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2019 | chr1 | 108931959 | |||||
chr1:108932093
|
T | C | 5 | a0002c0002t0011a0002c0002t0017a0002c0002t0026others(2): Show | 10 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2153T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2153 | chr1 | 108932093 | |||||
chr1:108932110
|
T | TA | 12 | a0002c0002t0011a0002c0002t0017a0002c0002t0018others(9): Show | 19 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2176dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2177 | INFO_REALIGN_3_PRIME | chr1 | 108932110 | ||||
chr1:108932113
|
A | AAAAT | 3 | a0004c0004t0004a0004c0004t0013a0004c0004t0031 | 14 | HG02886.hp1 HG02970.hp1 HG03490.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2178dupAATA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2179 | INFO_REALIGN_3_PRIME | chr1 | 108932113 | ||||
chr1:108932122
|
A | T | 1 | a0002c0010t0032 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2182A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2182 | chr1 | 108932122 | |||||
chr1:108932545
|
T | G | 1 | a0009c0013t0050 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2605T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2605 | chr1 | 108932545 | |||||
chr1:108932548
|
A | T | 1 | a0001c0001t0042 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2608A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2608 | chr1 | 108932548 | |||||
chr1:108932805
|
T | C | 2 | a0004c0004t0022a0004c0004t0034 | 3 | HG02615.hp2 HG03579.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2865T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2865 | chr1 | 108932805 | |||||
chr1:108932814
|
T | C | 2 | a0001c0001t0029a0001c0001t0030 | 2 | HG00741.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2874T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2874 | chr1 | 108932814 | |||||
chr1:108932826
|
T | C | 1 | a0001c0001t0038 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2886T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2886 | chr1 | 108932826 | |||||
chr1:108933081
|
GCTTAAGC others(139): Show |
G | 7 | a0002c0002t0006a0002c0002t0009a0002c0002t0019others(4): Show | 23 | HG01099.hp1 HG01346.hp2 HG01515.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3425_*3570del | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3425 | INFO_REALIGN_3_PRIME | chr1 | 108933081 | ||||
chr1:108933209
|
C | CTGCATTT others(139): Show |
1 | a0002c0002t0005 | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3414_*3415insTTGC others(142): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3415 | INFO_REALIGN_3_PRIME | chr1 | 108933209 | ||||
chr1:108933287
|
G | A | 1 | a0002c0010t0032 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3347 | chr1 | 108933287 | |||||
chr1:108933392
|
C | G | 1 | a0001c0001t0041 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3452C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3452 | chr1 | 108933392 | |||||
chr1:108933453
|
T | C | 1 | a0003c0003t0049 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3513T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3513 | chr1 | 108933453 | |||||
chr1:108933651
|
T | C | 1 | a0002c0002t0005 | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3711T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3711 | chr1 | 108933651 | |||||
chr1:108933676
|
G | C | 1 | a0004c0004t0033 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3736G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3736 | chr1 | 108933676 | |||||
chr1:108933733
|
T | C | 4 | a0004c0004t0004a0004c0004t0013a0004c0004t0031others(1): Show | 15 | HG02886.hp1 HG02970.hp1 HG03098.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3793T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3793 | chr1 | 108933733 | |||||
chr1:108933741
|
A | G | 33 | a0002c0002t0005a0002c0002t0006a0002c0002t0009others(30): Show | 98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*3801A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3801 | chr1 | 108933741 | |||||
chr1:108933828
|
T | C | 2 | a0001c0001t0016a0010c0012t0016 | 3 | NA18959.hp1 NA18972.hp1 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3888T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3888 | chr1 | 108933828 | |||||
chr1:108934069
|
C | T | 1 | a0001c0001t0040 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4129C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4129 | chr1 | 108934069 | |||||
chr1:108934158
|
C | T | 31 | a0002c0002t0005a0002c0002t0006a0002c0002t0009others(28): Show | 96 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4218C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4218 | chr1 | 108934158 | |||||
chr1:108934223
|
C | T | 1 | a0002c0010t0032 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4283C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4283 | chr1 | 108934223 | |||||
chr1:108934316
|
T | C | 12 | a0002c0002t0011a0002c0002t0017a0002c0002t0018others(9): Show | 19 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4376T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4376 | chr1 | 108934316 | |||||
chr1:108934495
|
C | T | 1 | a0001c0001t0039 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4555C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4555 | chr1 | 108934495 | |||||
chr1:108934529
|
G | A | 4 | a0004c0004t0004a0004c0004t0013a0004c0004t0031others(1): Show | 15 | HG02886.hp1 HG02970.hp1 HG03098.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4589G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4589 | chr1 | 108934529 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:108877253
|
C | T | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-249+25C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877253 | ||||||
chr1:108877330
|
G | C | 1 | a0001c0001t0002g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-249+102G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877330 | ||||||
chr1:108877466
|
G | A | 1 | a0004c0004t0013g0001 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-249+238G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877466 | ||||||
chr1:108877514
|
CT | C | 241 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(238): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-249+299delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 108877514 | |||||
chr1:108877527
|
T | C | 5 | a0002c0002t0018g0016a0002c0002t0045g0019a0006c0008t0018g0018others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-249+299T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877527 | ||||||
chr1:108877967
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-249+739C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877967 | ||||||
chr1:108877978
|
A | T | 9 | a0001c0001t0001g0208a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 9 | HG00438.hp2 HG00544.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-249+750A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877978 | ||||||
chr1:108878035
|
G | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02523.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-249+807G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108878035 | ||||||
chr1:108878455
|
A | C | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-249+1227A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108878455 | ||||||
chr1:108879069
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-249+1841A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879069 | ||||||
chr1:108879279
|
C | T | 1 | a0002c0002t0005g0014 | 2 | HG01123.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.-249+2051C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879279 | ||||||
chr1:108879283
|
G | A | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-249+2055G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879283 | ||||||
chr1:108879308
|
G | A | 93 | a0001c0001t0023g0049a0001c0001t0023g0050a0002c0002t0002g0024others(90): Show | 101 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(98): Show |
intron_variant | MODIFIER | c.-249+2080G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879308 | ||||||
chr1:108879452
|
T | G | 1 | a0001c0001t0039g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-249+2224T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879452 | ||||||
chr1:108879600
|
C | T | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-249+2372C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879600 | ||||||
chr1:108879823
|
A | G | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-249+2595A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879823 | ||||||
chr1:108879991
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-249+2763T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879991 | ||||||
chr1:108880208
|
A | G | 1 | a0001c0001t0041g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-249+2980A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880208 | ||||||
chr1:108880314
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-249+3086G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880314 | ||||||
chr1:108880430
|
A | C | 10 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(7): Show | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-249+3202A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880430 | ||||||
chr1:108880455
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-249+3227G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880455 | ||||||
chr1:108880579
|
C | CA | 65 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(62): Show | 65 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-249+3365dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 108880579 | |||||
chr1:108880579
|
C | CAAA | 6 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(3): Show | 7 | HG02258.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-249+3363_-249+336 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 108880579 | |||||
chr1:108880746
|
G | T | 1 | a0003c0003t0003g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-249+3518G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880746 | ||||||
chr1:108880944
|
A | T | 3 | a0002c0002t0006g0051a0002c0002t0006g0052a0002c0002t0006g0053 | 3 | NA18965.hp1 NA18968.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-249+3716A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880944 | ||||||
chr1:108881343
|
A | G | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-248-3932A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881343 | ||||||
chr1:108881354
|
A | G | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-248-3921A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881354 | ||||||
chr1:108881460
|
A | G | 1 | a0003c0003t0003g0244 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-248-3815A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881460 | ||||||
chr1:108881858
|
A | T | 2 | a0001c0001t0023g0049a0001c0001t0023g0050 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-248-3417A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881858 | ||||||
chr1:108882279
|
A | G | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-248-2996A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882279 | ||||||
chr1:108882280
|
T | A | 18 | a0001c0001t0001g0208a0001c0001t0001g0215a0001c0001t0001g0216others(15): Show | 18 | HG00438.hp2 HG00544.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-248-2995T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882280 | ||||||
chr1:108882325
|
A | G | 1 | a0002c0005t0008g0058 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-248-2950A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882325 | ||||||
chr1:108882344
|
A | G | 29 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(26): Show | 34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.-248-2931A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882344 | ||||||
chr1:108882521
|
A | G | 10 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(7): Show | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-248-2754A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882521 | ||||||
chr1:108882548
|
T | C | 1 | a0002c0002t0018g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-248-2727T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882548 | ||||||
chr1:108882573
|
T | C | 2 | a0002c0006t0010g0020a0002c0006t0010g0021 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-248-2702T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882573 | ||||||
chr1:108882696
|
C | T | 10 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(7): Show | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-248-2579C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882696 | ||||||
chr1:108882738
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-248-2537A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882738 | ||||||
chr1:108882978
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-248-2297G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882978 | ||||||
chr1:108883137
|
T | A | 1 | a0004c0004t0004g0193 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-248-2138T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108883137 | ||||||
chr1:108883331
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-248-1944T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108883331 | ||||||
chr1:108883666
|
G | A | 72 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(69): Show | 78 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.-248-1609G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108883666 | ||||||
chr1:108884004
|
C | T | 1 | a0001c0001t0002g0076 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-248-1271C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884004 | ||||||
chr1:108884035
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-248-1240C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884035 | ||||||
chr1:108884049
|
T | A | 5 | a0002c0002t0018g0016a0002c0002t0045g0019a0006c0008t0018g0018others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-248-1226T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884049 | ||||||
chr1:108884226
|
G | A | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-248-1049G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884226 | ||||||
chr1:108884421
|
A | T | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-248-854A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884421 | ||||||
chr1:108884612
|
A | G | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.-248-663A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884612 | ||||||
chr1:108884639
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-248-636G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884639 | ||||||
chr1:108884688
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-248-587T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884688 | ||||||
chr1:108884836
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-248-439A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884836 | ||||||
chr1:108885096
|
C | A | 1 | a0004c0004t0034g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-248-179C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108885096 | ||||||
chr1:108885096
|
C | G | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-248-179C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108885096 | ||||||
chr1:108885119
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-248-156C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108885119 | ||||||
chr1:108885627
|
G | A | 88 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(85): Show | 95 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(92): Show |
intron_variant | MODIFIER | c.56+49G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108885627 | ||||||
chr1:108885722
|
G | GT | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.56+145dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108885722 | |||||
chr1:108885953
|
T | G | 1 | a0002c0002t0017g0022 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.56+375T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108885953 | ||||||
chr1:108886037
|
A | T | 2 | a0002c0006t0010g0004a0002c0006t0010g0043 | 3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.56+459A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886037 | ||||||
chr1:108886134
|
A | G | 3 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0117 | 3 | HG01169.hp2 HG01516.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.56+556A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886134 | ||||||
chr1:108886485
|
G | A | 6 | a0004c0004t0004g0011a0004c0004t0004g0194a0004c0004t0004g0195others(3): Show | 8 | HG03490.hp2 HG03492.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+907G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886485 | ||||||
chr1:108886486
|
G | GGAGAAAT | 5 | a0001c0001t0001g0007a0001c0001t0001g0078a0001c0001t0001g0121others(2): Show | 5 | HG01175.hp2 HG01978.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+908_56+909insGA others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886486 | ||||||
chr1:108886652
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56+1074G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886652 | ||||||
chr1:108886721
|
C | T | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+1143C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886721 | ||||||
chr1:108886863
|
A | AGT | 3 | a0002c0005t0014g0060a0004c0004t0022g0063a0004c0004t0022g0064 | 3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.56+1300_56+1301dup others(2): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108886863 | |||||
chr1:108886950
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.56+1372G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886950 | ||||||
chr1:108887011
|
C | T | 1 | a0004c0004t0033g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.56+1433C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887011 | ||||||
chr1:108887043
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.56+1465C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887043 | ||||||
chr1:108887157
|
G | A | 1 | a0004c0004t0034g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.56+1579G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887157 | ||||||
chr1:108887214
|
C | A | 1 | a0006c0008t0044g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56+1636C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887214 | ||||||
chr1:108887355
|
G | A | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+1777G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887355 | ||||||
chr1:108887438
|
C | T | 3 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0117 | 3 | HG01169.hp2 HG01516.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.56+1860C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887438 | ||||||
chr1:108887760
|
C | G | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.56+2182C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887760 | ||||||
chr1:108887793
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.56+2215A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887793 | ||||||
chr1:108887963
|
C | G | 90 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(87): Show | 98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.56+2385C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887963 | ||||||
chr1:108887987
|
G | A | 3 | a0006c0008t0018g0018a0006c0008t0018g0218a0006c0008t0044g0017 | 3 | HG01109.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56+2409G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887987 | ||||||
chr1:108888029
|
G | A | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+2451G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888029 | ||||||
chr1:108888032
|
G | A | 14 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(11): Show | 15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.56+2454G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888032 | ||||||
chr1:108888224
|
A | C | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.56+2646A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888224 | ||||||
chr1:108888351
|
CT | C | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+2780delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108888351 | |||||
chr1:108888488
|
C | A | 5 | a0003c0003t0003g0230a0003c0003t0021g0227a0003c0003t0021g0228others(2): Show | 5 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+2910C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888488 | ||||||
chr1:108888492
|
T | C | 244 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(241): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.56+2914T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888492 | ||||||
chr1:108888948
|
A | T | 1 | a0004c0004t0013g0001 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.56+3370A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888948 | ||||||
chr1:108889225
|
G | A | 9 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(6): Show | 10 | HG01433.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.56+3647G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889225 | ||||||
chr1:108889466
|
C | T | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.56+3888C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889466 | ||||||
chr1:108889586
|
G | A | 1 | a0001c0001t0007g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.56+4008G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889586 | ||||||
chr1:108889789
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.56+4211C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889789 | ||||||
chr1:108890021
|
A | G | 5 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+4443A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890021 | ||||||
chr1:108890033
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.56+4455T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890033 | ||||||
chr1:108890394
|
G | A | 1 | a0003c0003t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.56+4816G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890394 | ||||||
chr1:108890592
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0126 | 2 | NA18947.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.56+5014G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890592 | ||||||
chr1:108890748
|
A | G | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.56+5170A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890748 | ||||||
chr1:108890880
|
TA | T | 16 | a0001c0001t0002g0076a0001c0001t0002g0114a0003c0003t0003g0232others(13): Show | 16 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.56+5311delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108890880 | |||||
chr1:108890913
|
T | C | 1 | a0002c0002t0009g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.56+5335T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890913 | ||||||
chr1:108890993
|
G | T | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+5415G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890993 | ||||||
chr1:108891154
|
C | T | 10 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(7): Show | 11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+5576C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891154 | ||||||
chr1:108891367
|
C | G | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-5497C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891367 | ||||||
chr1:108891486
|
G | T | 1 | a0004c0004t0034g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.57-5378G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891486 | ||||||
chr1:108891664
|
A | AT | 45 | a0001c0001t0001g0122a0001c0001t0001g0180a0001c0001t0001g0188others(42): Show | 48 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.57-5180dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | |||||
chr1:108891664
|
A | ATT | 18 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(15): Show | 22 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.57-5181_57-5180dup others(2): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | |||||
chr1:108891664
|
A | ATTTT | 14 | a0003c0003t0003g0232a0003c0003t0003g0233a0003c0003t0003g0236others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-5183_57-5180dup others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | |||||
chr1:108891664
|
A | ATTTTT | 17 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.57-5184_57-5180dup others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | |||||
chr1:108891750
|
C | A | 12 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(9): Show | 14 | HG02886.hp1 HG02970.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-5114C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891750 | ||||||
chr1:108891754
|
C | G | 5 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.57-5110C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891754 | ||||||
chr1:108892090
|
C | T | 14 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(11): Show | 15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.57-4774C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892090 | ||||||
chr1:108892204
|
T | C | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-4660T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892204 | ||||||
chr1:108892323
|
G | A | 1 | a0003c0003t0003g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.57-4541G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892323 | ||||||
chr1:108892404
|
A | G | 1 | a0001c0001t0029g0179 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.57-4460A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892404 | ||||||
chr1:108892474
|
G | GA | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.57-4386dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108892474 | |||||
chr1:108892512
|
T | C | 10 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(7): Show | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.57-4352T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892512 | ||||||
chr1:108892867
|
C | T | 3 | a0001c0001t0002g0113a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.57-3997C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892867 | ||||||
chr1:108893226
|
T | C | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-3638T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893226 | ||||||
chr1:108893315
|
C | T | 1 | a0004c0004t0033g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57-3549C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893315 | ||||||
chr1:108893506
|
A | G | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-3358A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893506 | ||||||
chr1:108893510
|
G | C | 1 | a0002c0002t0011g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.57-3354G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893510 | ||||||
chr1:108893764
|
T | C | 1 | a0003c0003t0003g0233 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.57-3100T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893764 | ||||||
chr1:108893769
|
T | C | 29 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(26): Show | 34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.57-3095T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893769 | ||||||
chr1:108893829
|
C | T | 1 | a0001c0001t0012g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.57-3035C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893829 | ||||||
chr1:108894039
|
A | G | 1 | a0002c0006t0010g0004 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.57-2825A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894039 | ||||||
chr1:108894212
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57-2652A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894212 | ||||||
chr1:108894651
|
T | C | 10 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(7): Show | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.57-2213T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894651 | ||||||
chr1:108894753
|
TA | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0216a0001c0001t0002g0110others(3): Show | 6 | HG01099.hp2 HG03195.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.57-2099delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108894753 | |||||
chr1:108894771
|
C | T | 2 | a0003c0003t0003g0242a0003c0003t0003g0243 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.57-2093C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894771 | ||||||
chr1:108895428
|
C | CA | 93 | a0001c0001t0001g0188a0001c0001t0023g0049a0001c0001t0023g0050others(90): Show | 101 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(98): Show |
intron_variant | MODIFIER | c.57-1436_57-1435ins others(1): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895428 | ||||||
chr1:108895458
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.57-1406G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895458 | ||||||
chr1:108895496
|
G | A | 3 | a0004c0004t0004g0197a0004c0004t0004g0198a0004c0004t0004g0199 | 3 | HG03491.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.57-1368G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895496 | ||||||
chr1:108895610
|
T | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0127 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.57-1254T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895610 | ||||||
chr1:108896155
|
C | T | 1 | a0002c0005t0051g0057 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.57-709C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896155 | ||||||
chr1:108896202
|
T | G | 1 | a0003c0003t0003g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.57-662T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896202 | ||||||
chr1:108896390
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.57-474C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896390 | ||||||
chr1:108896450
|
T | A | 2 | a0002c0006t0010g0020a0002c0006t0010g0021 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.57-414T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896450 | ||||||
chr1:108896740
|
C | T | 2 | a0002c0006t0010g0004a0002c0006t0010g0043 | 3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.57-124C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896740 | ||||||
chr1:108896778
|
C | T | 14 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(11): Show | 15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.57-86C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896778 | ||||||
chr1:108896779
|
G | A | 1 | a0004c0004t0004g0194 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.57-85G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896779 | ||||||
chr1:108897090
|
T | C | 10 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(7): Show | 11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.278+5T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897090 | ||||||
chr1:108897156
|
A | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG00099.hp2 HG01496.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.278+71A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897156 | ||||||
chr1:108897250
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.278+165A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897250 | ||||||
chr1:108897267
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.278+182G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897267 | ||||||
chr1:108897408
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.279-84T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897408 | ||||||
chr1:108898118
|
A | G | 13 | a0002c0010t0032g0205a0004c0004t0004g0011a0004c0004t0004g0193others(10): Show | 15 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.557+17A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 5/14 | chr1 | 108898118 | ||||||
chr1:108898246
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.557+145T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 5/14 | chr1 | 108898246 | ||||||
chr1:108898359
|
T | A | 1 | a0002c0002t0002g0024 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.557+258T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 5/14 | chr1 | 108898359 | ||||||
chr1:108898835
|
T | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.682-44T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 6/14 | chr1 | 108898835 | ||||||
chr1:108899398
|
C | T | 2 | a0001c0001t0002g0109a0001c0001t0028g0108 | 2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.797+404C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899398 | ||||||
chr1:108899528
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.797+534T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899528 | ||||||
chr1:108899656
|
A | G | 2 | a0001c0001t0023g0049a0001c0001t0023g0050 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.797+662A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899656 | ||||||
chr1:108899731
|
T | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0180 | 2 | HG02040.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.797+737T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899731 | ||||||
chr1:108900032
|
A | G | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.797+1038A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900032 | ||||||
chr1:108900137
|
A | G | 3 | a0001c0001t0002g0081a0001c0001t0002g0118a0001c0001t0002g0127 | 3 | HG00738.hp1 HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.797+1143A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900137 | ||||||
chr1:108900187
|
A | G | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.797+1193A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900187 | ||||||
chr1:108900233
|
A | AT | 18 | a0001c0001t0001g0078a0001c0001t0001g0215a0001c0001t0002g0081others(15): Show | 20 | HG02055.hp1 HG02738.hp1 HG02886.hp1 others(17): Show |
intron_variant | MODIFIER | c.797+1261dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 108900233 | |||||
chr1:108900233
|
AT | A | 9 | a0001c0001t0001g0131a0001c0014t0001g0132a0002c0002t0006g0051others(6): Show | 9 | HG01099.hp1 HG01167.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.797+1261delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 108900233 | |||||
chr1:108900256
|
A | T | 2 | a0002c0006t0010g0004a0002c0006t0010g0043 | 3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.797+1262A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900256 | ||||||
chr1:108900333
|
C | T | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.797+1339C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900333 | ||||||
chr1:108900481
|
C | T | 2 | a0001c0001t0023g0049a0001c0001t0023g0050 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.798-1309C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900481 | ||||||
chr1:108900490
|
C | T | 5 | a0002c0002t0009g0036a0002c0002t0009g0038a0002c0002t0019g0034others(2): Show | 5 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.798-1300C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900490 | ||||||
chr1:108900695
|
T | C | 2 | a0001c0001t0001g0188a0008c0011t0006g0025 | 2 | NA18948.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.798-1095T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900695 | ||||||
chr1:108900906
|
TG | T | 14 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(11): Show | 15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.798-883delG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900906 | ||||||
chr1:108901090
|
C | T | 1 | a0004c0004t0034g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.798-700C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901090 | ||||||
chr1:108901110
|
A | T | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.798-680A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901110 | ||||||
chr1:108901236
|
C | T | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.798-554C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901236 | ||||||
chr1:108901241
|
G | A | 7 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(4): Show | 8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.798-549G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901241 | ||||||
chr1:108901407
|
C | T | 1 | a0004c0004t0022g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.798-383C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901407 | ||||||
chr1:108901676
|
A | G | 15 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.798-114A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901676 | ||||||
chr1:108901748
|
A | T | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.798-42A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901748 | ||||||
chr1:108902176
|
A | G | 2 | a0002c0006t0010g0004a0002c0006t0010g0043 | 3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.953+231A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108902176 | ||||||
chr1:108902239
|
G | T | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.953+294G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108902239 | ||||||
chr1:108902379
|
C | CA | 26 | a0001c0001t0001g0133a0001c0001t0001g0186a0001c0001t0001g0215others(23): Show | 31 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.953+452dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 108902379 | |||||
chr1:108902379
|
CA | C | 6 | a0001c0001t0001g0168a0001c0001t0002g0075a0002c0002t0009g0038others(3): Show | 6 | HG01516.hp1 HG02735.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.953+452delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 108902379 | |||||
chr1:108902744
|
C | T | 1 | a0003c0003t0003g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.954-382C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108902744 | ||||||
chr1:108903011
|
A | C | 1 | a0002c0002t0026g0030 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.954-115A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108903011 | ||||||
chr1:108903084
|
T | G | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.954-42T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108903084 | ||||||
chr1:108903107
|
G | T | 1 | a0001c0001t0007g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.954-19G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108903107 | ||||||
chr1:108903286
|
G | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0110 | 3 | NA19009.hp2 NA19079.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1062+52G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903286 | ||||||
chr1:108903286
|
G | C | 5 | a0002c0002t0009g0036a0002c0002t0009g0038a0002c0002t0019g0034others(2): Show | 5 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062+52G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903286 | ||||||
chr1:108903331
|
A | G | 7 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(4): Show | 8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1062+97A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903331 | ||||||
chr1:108903393
|
A | G | 3 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074 | 3 | NA18947.hp1 NA19068.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1062+159A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903393 | ||||||
chr1:108903423
|
C | G | 89 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(86): Show | 97 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(94): Show |
intron_variant | MODIFIER | c.1062+189C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903423 | ||||||
chr1:108903518
|
G | A | 12 | a0003c0003t0003g0232a0003c0003t0003g0233a0003c0003t0003g0236others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+284G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903518 | ||||||
chr1:108903835
|
T | C | 1 | a0001c0001t0015g0085 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1063-290T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903835 | ||||||
chr1:108903853
|
G | A | 1 | a0002c0005t0008g0054 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1063-272G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903853 | ||||||
chr1:108904502
|
C | G | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192+248C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108904502 | ||||||
chr1:108904979
|
TA | T | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1192+733delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108904979 | |||||
chr1:108905001
|
T | C | 1 | a0003c0003t0003g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1192+747T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905001 | ||||||
chr1:108905022
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1192+768A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905022 | ||||||
chr1:108905078
|
GT | G | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192+825delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905078 | ||||||
chr1:108905317
|
T | C | 1 | a0003c0003t0003g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1192+1063T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905317 | ||||||
chr1:108905377
|
C | G | 1 | a0001c0001t0016g0214 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1192+1123C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905377 | ||||||
chr1:108905442
|
A | G | 14 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(11): Show | 15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.1192+1188A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905442 | ||||||
chr1:108905452
|
G | A | 2 | a0002c0006t0010g0020a0002c0006t0010g0021 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1192+1198G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905452 | ||||||
chr1:108905575
|
C | T | 4 | a0002c0002t0018g0016a0006c0008t0018g0018a0006c0008t0018g0218others(1): Show | 4 | HG01109.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+1321C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905575 | ||||||
chr1:108905876
|
T | C | 7 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(4): Show | 8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+1622T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905876 | ||||||
chr1:108905913
|
G | T | 1 | a0002c0010t0032g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1192+1659G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905913 | ||||||
chr1:108906165
|
G | GGAAA | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+1911_1192+191 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906165 | ||||||
chr1:108906199
|
A | T | 7 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(4): Show | 8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+1945A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906199 | ||||||
chr1:108906279
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1192+2025T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906279 | ||||||
chr1:108906556
|
CT | C | 97 | a0001c0001t0001g0120a0001c0001t0001g0134a0001c0001t0001g0171others(94): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.1192+2320delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108906556 | |||||
chr1:108906574
|
T | C | 1 | a0003c0003t0003g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1192+2320T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906574 | ||||||
chr1:108906684
|
C | T | 7 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(4): Show | 8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+2430C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906684 | ||||||
chr1:108907002
|
CAGTT | C | 5 | a0003c0003t0003g0238a0003c0003t0003g0239a0003c0003t0003g0241others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192+2753_1192+275 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108907002 | |||||
chr1:108907028
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1192+2774G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907028 | ||||||
chr1:108907133
|
A | G | 74 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0005g0012others(71): Show | 80 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.1192+2879A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907133 | ||||||
chr1:108907301
|
G | A | 1 | a0004c0004t0004g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1192+3047G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907301 | ||||||
chr1:108907372
|
TC | T | 3 | a0004c0004t0004g0193a0004c0004t0004g0198a0004c0004t0004g0199 | 3 | HG03491.hp2 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1192+3120delC | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108907372 | |||||
chr1:108907395
|
G | A | 10 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(7): Show | 11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192+3141G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907395 | ||||||
chr1:108907443
|
C | G | 92 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0005g0012others(89): Show | 100 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(97): Show |
intron_variant | MODIFIER | c.1192+3189C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907443 | ||||||
chr1:108907527
|
T | A | 74 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0005g0012others(71): Show | 80 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.1192+3273T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907527 | ||||||
chr1:108907862
|
C | T | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+3608C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907862 | ||||||
chr1:108908094
|
G | A | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192+3840G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908094 | ||||||
chr1:108908185
|
C | T | 10 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(7): Show | 11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192+3931C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908185 | ||||||
chr1:108908264
|
G | C | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192+4010G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908264 | ||||||
chr1:108908357
|
C | G | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+4103C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908357 | ||||||
chr1:108908409
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1192+4155C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908409 | ||||||
chr1:108908466
|
G | A | 1 | a0002c0002t0019g0035 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1192+4212G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908466 | ||||||
chr1:108908496
|
A | G | 2 | a0001c0001t0023g0049a0001c0001t0023g0050 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1192+4242A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908496 | ||||||
chr1:108908629
|
C | G | 35 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(32): Show | 35 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1192+4375C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908629 | ||||||
chr1:108908680
|
T | C | 87 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0005g0012others(84): Show | 94 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1192+4426T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908680 | ||||||
chr1:108908687
|
A | G | 1 | a0004c0004t0033g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1192+4433A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908687 | ||||||
chr1:108908722
|
A | AACACACA others(37): Show |
1 | a0003c0003t0003g0244 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1192+4473_1192+447 others(48): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908722 | |||||
chr1:108908728
|
A | AACACACA others(5): Show |
19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(9): Show |
8 | a0002c0002t0006g0002a0002c0002t0006g0023a0002c0002t0006g0028others(5): Show | 8 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(11): Show |
5 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0051others(2): Show | 5 | NA18965.hp1 NA18968.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(13): Show |
2 | a0002c0002t0006g0031a0008c0011t0006g0025 | 2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(17): Show |
1 | a0002c0006t0010g0004 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(28): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(19): Show |
3 | a0002c0002t0011g0048a0002c0006t0010g0043a0003c0003t0003g0237 | 3 | HG01175.hp1 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(30): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(21): Show |
4 | a0002c0006t0010g0020a0002c0006t0010g0021a0004c0004t0034g0032others(1): Show | 4 | HG02615.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(32): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(23): Show |
14 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(11): Show | 14 | HG01099.hp1 HG01099.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(34): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(25): Show |
10 | a0002c0002t0020g0003a0002c0002t0020g0039a0002c0005t0008g0005others(7): Show | 12 | HG01109.hp1 HG01433.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(36): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(27): Show |
6 | a0002c0002t0045g0019a0002c0005t0014g0061a0002c0005t0014g0062others(3): Show | 6 | HG00280.hp2 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(38): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(29): Show |
7 | a0002c0002t0018g0016a0002c0005t0008g0055a0002c0005t0008g0058others(4): Show | 7 | HG00140.hp1 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(40): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(31): Show |
1 | a0006c0008t0044g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1192+4484_1192+448 others(42): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(35): Show |
2 | a0003c0003t0003g0236a0003c0003t0003g0245 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(46): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(37): Show |
2 | a0003c0003t0003g0233a0003c0003t0048g0235 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(48): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(39): Show |
2 | a0003c0003t0003g0238a0003c0003t0003g0243 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(50): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(41): Show |
2 | a0003c0003t0003g0232a0003c0003t0003g0239 | 2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(52): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(43): Show |
1 | a0003c0003t0003g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1192+4484_1192+448 others(54): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | AACACACA others(49): Show |
1 | a0003c0003t0003g0240 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1192+4484_1192+448 others(60): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | |||||
chr1:108908728
|
A | ACACACAC others(10): Show |
1 | a0002c0002t0017g0029 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1192+4474_1192+447 others(21): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908728 | ||||||
chr1:108908728
|
A | C | 1 | a0003c0003t0003g0244 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1192+4474A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908728 | ||||||
chr1:108908897
|
G | A | 13 | a0002c0010t0032g0205a0004c0004t0004g0011a0004c0004t0004g0193others(10): Show | 15 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.1192+4643G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908897 | ||||||
chr1:108908908
|
G | A | 7 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(4): Show | 8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+4654G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908908 | ||||||
chr1:108908963
|
C | G | 14 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(11): Show | 15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.1192+4709C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908963 | ||||||
chr1:108908980
|
A | T | 12 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(9): Show | 13 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192+4726A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908980 | ||||||
chr1:108908988
|
A | G | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+4734A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908988 | ||||||
chr1:108909054
|
A | G | 244 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(241): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1192+4800A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909054 | ||||||
chr1:108909079
|
C | T | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1192+4825C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909079 | ||||||
chr1:108909098
|
T | C | 88 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0005g0012others(85): Show | 95 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(92): Show |
intron_variant | MODIFIER | c.1192+4844T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909098 | ||||||
chr1:108909146
|
G | A | 5 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192+4892G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909146 | ||||||
chr1:108909185
|
TTTG | T | 13 | a0002c0010t0032g0205a0004c0004t0004g0011a0004c0004t0004g0193others(10): Show | 15 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.1192+4936_1192+493 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909185 | |||||
chr1:108909299
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0189 | 3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1193-5039T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909299 | ||||||
chr1:108909406
|
G | A | 1 | a0004c0004t0033g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1193-4932G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909406 | ||||||
chr1:108909567
|
T | A | 1 | a0001c0001t0030g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1193-4771T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909567 | ||||||
chr1:108909597
|
A | G | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-4741A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909597 | ||||||
chr1:108909644
|
C | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0189 | 3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1193-4694C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909644 | ||||||
chr1:108909902
|
C | CA | 31 | a0001c0001t0001g0067a0001c0001t0001g0122a0001c0001t0001g0124others(28): Show | 32 | HG00544.hp1 HG01109.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1193-4411dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | |||||
chr1:108909902
|
CA | C | 10 | a0002c0002t0009g0033a0002c0002t0009g0040a0002c0002t0009g0041others(7): Show | 10 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1193-4411delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | |||||
chr1:108909902
|
CAAAAAAA | C | 4 | a0002c0002t0005g0013a0002c0002t0005g0202a0002c0002t0005g0203others(1): Show | 5 | HG02258.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-4417_1193-441 others(11): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | |||||
chr1:108909902
|
CAAAAAAA others(5): Show |
C | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-4422_1193-441 others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | |||||
chr1:108909921
|
A | G | 5 | a0002c0002t0018g0016a0002c0002t0045g0019a0006c0008t0018g0018others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-4417A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909921 | ||||||
chr1:108909922
|
A | G | 5 | a0002c0002t0018g0016a0002c0002t0045g0019a0006c0008t0018g0018others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-4416A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909922 | ||||||
chr1:108909940
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1193-4398A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909940 | ||||||
chr1:108909974
|
A | G | 1 | a0001c0001t0038g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1193-4364A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909974 | ||||||
chr1:108909981
|
C | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0096a0001c0001t0001g0098others(3): Show | 7 | HG01496.hp1 HG01978.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-4357C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909981 | ||||||
chr1:108910081
|
T | C | 1 | a0003c0003t0003g0237 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1193-4257T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910081 | ||||||
chr1:108910082
|
T | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0189 | 3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1193-4256T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910082 | ||||||
chr1:108910123
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0189a0002c0005t0008g0005others(9): Show | 14 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-4215T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910123 | ||||||
chr1:108910383
|
C | CA | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1193-3950dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108910383 | |||||
chr1:108910507
|
T | C | 29 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(26): Show | 34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1193-3831T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910507 | ||||||
chr1:108910591
|
G | A | 3 | a0002c0002t0009g0033a0002c0002t0009g0040a0002c0002t0009g0041 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1193-3747G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910591 | ||||||
chr1:108910815
|
A | C | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1193-3523A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910815 | ||||||
chr1:108910862
|
C | CA | 40 | a0001c0001t0001g0107a0001c0001t0001g0120a0001c0001t0001g0134others(37): Show | 42 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1193-3462dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108910862 | |||||
chr1:108911103
|
CTAATA | C | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1193-3231_1193-322 others(9): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911103 | |||||
chr1:108911158
|
A | G | 1 | a0007c0009t0001g0166 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1193-3180A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911158 | ||||||
chr1:108911168
|
A | G | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-3170A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911168 | ||||||
chr1:108911214
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1193-3124G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911214 | ||||||
chr1:108911265
|
C | T | 1 | a0001c0001t0016g0175 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1193-3073C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911265 | ||||||
chr1:108911357
|
G | A | 16 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0006g0002others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-2981G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911357 | ||||||
chr1:108911663
|
T | C | 87 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0005g0012others(84): Show | 94 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1193-2675T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911663 | ||||||
chr1:108911664
|
G | A | 2 | a0003c0003t0003g0242a0003c0003t0003g0243 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1193-2674G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911664 | ||||||
chr1:108911734
|
G | A | 29 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(26): Show | 34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1193-2604G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911734 | ||||||
chr1:108911799
|
A | AT | 161 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1193-2515dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | |||||
chr1:108911799
|
A | ATT | 48 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0120others(45): Show | 54 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1193-2516_1193-251 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | |||||
chr1:108911799
|
A | ATTT | 31 | a0001c0001t0002g0114a0002c0002t0006g0002a0002c0002t0006g0028others(28): Show | 33 | HG01099.hp1 HG01109.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.1193-2517_1193-251 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | |||||
chr1:108911799
|
A | ATTTT | 5 | a0002c0010t0032g0205a0004c0004t0022g0063a0004c0004t0022g0064others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1193-2518_1193-251 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | |||||
chr1:108911853
|
G | A | 1 | a0001c0001t0052g0100 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1193-2485G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911853 | ||||||
chr1:108911949
|
G | C | 5 | a0003c0003t0003g0230a0003c0003t0021g0227a0003c0003t0021g0228others(2): Show | 5 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-2389G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911949 | ||||||
chr1:108912343
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-1995G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912343 | ||||||
chr1:108912476
|
G | C | 7 | a0002c0005t0008g0005a0002c0005t0008g0054a0002c0005t0008g0055others(4): Show | 8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193-1862G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912476 | ||||||
chr1:108912577
|
T | TA | 13 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0215others(10): Show | 16 | HG00738.hp2 HG01123.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1193-1743dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912577 | |||||
chr1:108912577
|
TA | T | 24 | a0002c0002t0006g0053a0002c0005t0014g0060a0002c0005t0014g0061others(21): Show | 24 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1193-1743delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912577 | |||||
chr1:108912577
|
TAA | T | 10 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(7): Show | 11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1193-1744_1193-174 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912577 | |||||
chr1:108912718
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1193-1620T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912718 | ||||||
chr1:108912757
|
G | A | 46 | a0001c0001t0001g0188a0001c0001t0001g0222a0001c0001t0023g0049others(43): Show | 49 | HG00140.hp1 HG00280.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1193-1581G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912757 | ||||||
chr1:108912872
|
C | G | 1 | a0001c0001t0002g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1193-1466C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912872 | ||||||
chr1:108912884
|
T | TA | 12 | a0001c0001t0015g0086a0001c0001t0046g0068a0002c0002t0020g0003others(9): Show | 14 | HG01109.hp2 HG01433.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-1442dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912884 | |||||
chr1:108912916
|
C | T | 16 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0031others(13): Show | 16 | HG01109.hp1 HG01346.hp2 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.1193-1422C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912916 | ||||||
chr1:108913001
|
A | AG | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1336dupG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108913001 | |||||
chr1:108913003
|
T | A | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1335T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913003 | ||||||
chr1:108913004
|
G | A | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1334G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913004 | ||||||
chr1:108913006
|
A | T | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1332A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913006 | ||||||
chr1:108913013
|
G | T | 128 | a0001c0001t0001g0161a0001c0001t0001g0188a0001c0001t0001g0208others(125): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1193-1325G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913013 | ||||||
chr1:108913035
|
A | G | 3 | a0001c0001t0002g0070a0001c0001t0002g0071a0001c0001t0002g0076 | 3 | NA18944.hp2 NA18974.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1193-1303A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913035 | ||||||
chr1:108913064
|
G | A | 11 | a0002c0002t0006g0023a0002c0002t0006g0028a0004c0004t0004g0011others(8): Show | 13 | HG01515.hp2 HG01517.hp1 HG02970.hp1 others(10): Show |
intron_variant | MODIFIER | c.1193-1274G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913064 | ||||||
chr1:108913155
|
C | T | 2 | a0002c0006t0010g0004a0002c0006t0010g0043 | 3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1193-1183C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913155 | ||||||
chr1:108913203
|
T | C | 2 | a0002c0006t0010g0004a0002c0006t0010g0043 | 3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1193-1135T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913203 | ||||||
chr1:108913216
|
C | T | 2 | a0001c0001t0023g0049a0001c0001t0023g0050 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1193-1122C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913216 | ||||||
chr1:108913237
|
C | T | 2 | a0001c0001t0023g0049a0001c0001t0023g0050 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1193-1101C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913237 | ||||||
chr1:108913250
|
A | T | 12 | a0002c0010t0032g0205a0004c0004t0004g0011a0004c0004t0004g0193others(9): Show | 14 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.1193-1088A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913250 | ||||||
chr1:108913311
|
A | C | 1 | a0004c0004t0034g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1193-1027A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913311 | ||||||
chr1:108913354
|
A | C | 1 | a0001c0001t0041g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1193-984A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913354 | ||||||
chr1:108913558
|
C | T | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1193-780C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913558 | ||||||
chr1:108913559
|
T | C | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1193-779T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913559 | ||||||
chr1:108913678
|
T | C | 1 | a0004c0004t0022g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1193-660T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913678 | ||||||
chr1:108913759
|
C | G | 6 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(3): Show | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1193-579C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913759 | ||||||
chr1:108913839
|
T | C | 1 | a0003c0003t0003g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1193-499T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913839 | ||||||
chr1:108913936
|
C | T | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1193-402C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913936 | ||||||
chr1:108913989
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1193-349T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913989 | ||||||
chr1:108914228
|
G | A | 76 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(73): Show | 84 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1193-110G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108914228 | ||||||
chr1:108914511
|
G | C | 1 | a0001c0001t0007g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1263+103G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914511 | ||||||
chr1:108914516
|
A | C | 1 | a0001c0001t0038g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1263+108A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914516 | ||||||
chr1:108914529
|
C | T | 55 | a0001c0001t0002g0006a0001c0001t0002g0015a0001c0001t0002g0066others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.1263+121C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914529 | ||||||
chr1:108914629
|
T | G | 5 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+221T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914629 | ||||||
chr1:108914809
|
A | G | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+401A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914809 | ||||||
chr1:108914819
|
C | T | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1263+411C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914819 | ||||||
chr1:108914888
|
G | A | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1263+480G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914888 | ||||||
chr1:108915007
|
G | A | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1263+599G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915007 | ||||||
chr1:108915151
|
T | A | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+743T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915151 | ||||||
chr1:108915303
|
G | A | 11 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0145others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.1263+895G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915303 | ||||||
chr1:108915326
|
G | A | 249 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1263+918G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915326 | ||||||
chr1:108915368
|
C | CA | 15 | a0001c0001t0001g0111a0001c0001t0001g0128a0001c0001t0001g0148others(12): Show | 15 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.1263+979dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | |||||
chr1:108915368
|
CA | C | 29 | a0001c0001t0001g0217a0001c0001t0002g0104a0001c0001t0002g0116others(26): Show | 29 | HG01099.hp1 HG01516.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1263+979delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | |||||
chr1:108915368
|
CAA | C | 51 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(48): Show | 57 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.1263+978_1263+979d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | |||||
chr1:108915368
|
CAAA | C | 14 | a0002c0002t0005g0203a0002c0002t0020g0003a0002c0002t0020g0039others(11): Show | 16 | HG01433.hp2 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1263+977_1263+979d others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | |||||
chr1:108915489
|
C | T | 5 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1081C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915489 | ||||||
chr1:108915522
|
G | A | 4 | a0002c0002t0005g0013a0002c0002t0005g0202a0002c0002t0005g0203others(1): Show | 5 | HG02258.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+1114G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915522 | ||||||
chr1:108915552
|
G | A | 18 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(15): Show | 21 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1263+1144G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915552 | ||||||
chr1:108915666
|
C | T | 5 | a0002c0002t0018g0016a0002c0002t0045g0019a0006c0008t0018g0018others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+1258C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915666 | ||||||
chr1:108915716
|
C | A | 4 | a0002c0002t0005g0013a0002c0002t0005g0202a0002c0002t0005g0203others(1): Show | 5 | HG02258.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+1308C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915716 | ||||||
chr1:108915770
|
A | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0189 | 3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1263+1362A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915770 | ||||||
chr1:108915967
|
C | T | 1 | a0009c0013t0050g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1263+1559C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915967 | ||||||
chr1:108915968
|
G | A | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1263+1560G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915968 | ||||||
chr1:108916078
|
C | CA | 68 | a0001c0001t0001g0216a0001c0001t0023g0049a0001c0001t0023g0050others(65): Show | 74 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.1263+1686dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916078 | |||||
chr1:108916078
|
C | CAA | 22 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(19): Show | 23 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1263+1685_1263+168 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916078 | |||||
chr1:108916078
|
C | CAAAA | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1683_1263+168 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916078 | |||||
chr1:108916260
|
G | GAA | 6 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(3): Show | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1263+1863_1263+186 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916260 | |||||
chr1:108916393
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG00280.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1263+1985A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916393 | ||||||
chr1:108916457
|
T | C | 7 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(4): Show | 10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1263+2049T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916457 | ||||||
chr1:108916674
|
A | T | 17 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(14): Show | 20 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1264-1939A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916674 | ||||||
chr1:108916832
|
T | A | 1 | a0001c0001t0002g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1264-1781T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916832 | ||||||
chr1:108917033
|
C | T | 1 | a0002c0005t0014g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1264-1580C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917033 | ||||||
chr1:108917057
|
T | G | 3 | a0002c0005t0014g0060a0002c0005t0014g0061a0002c0005t0014g0062 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1264-1556T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917057 | ||||||
chr1:108917290
|
G | A | 15 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(12): Show | 17 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(14): Show |
intron_variant | MODIFIER | c.1264-1323G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917290 | ||||||
chr1:108917334
|
G | A | 1 | a0004c0004t0033g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1264-1279G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917334 | ||||||
chr1:108917513
|
G | A | 1 | a0002c0010t0032g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1264-1100G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917513 | ||||||
chr1:108917525
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1264-1088C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917525 | ||||||
chr1:108917609
|
CACATATA others(29): Show |
C | 8 | a0002c0002t0020g0003a0002c0002t0020g0039a0002c0005t0008g0005others(5): Show | 10 | HG01433.hp2 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-1002_1264-967 others(39): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917609 | |||||
chr1:108917609
|
CACATATA others(31): Show |
C | 68 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(65): Show | 74 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.1264-1002_1264-965 others(41): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917609 | |||||
chr1:108917609
|
CACATATA others(33): Show |
C | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264-1002_1264-963 others(43): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917609 | |||||
chr1:108917611
|
C | CACACACA others(21): Show |
1 | a0001c0001t0002g0110 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(32): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(13): Show |
1 | a0001c0001t0001g0142 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(15): Show |
1 | a0001c0001t0002g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(13): Show |
1 | a0001c0001t0002g0099 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(17): Show |
1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(28): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(7): Show |
1 | a0001c0001t0001g0128 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(15): Show |
1 | a0001c0001t0001g0079 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(7): Show |
1 | a0010c0012t0016g0169 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(11): Show |
1 | a0001c0001t0030g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(13): Show |
1 | a0001c0001t0015g0085 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(15): Show |
1 | a0001c0001t0002g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(17): Show |
2 | a0001c0001t0002g0006a0001c0001t0015g0006 | 2 | HG01952.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(28): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACACA others(23): Show |
1 | a0001c0001t0002g0072 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(34): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACATA others(9): Show |
4 | a0001c0001t0001g0226a0001c0001t0002g0087a0001c0001t0002g0138others(1): Show | 4 | HG00741.hp2 HG02056.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACATA others(11): Show |
1 | a0001c0001t0041g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACATA others(19): Show |
2 | a0001c0001t0002g0073a0001c0001t0002g0212 | 2 | NA18939.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(30): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACACATA others(25): Show |
1 | a0001c0001t0001g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(36): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACATATA others(3): Show |
2 | a0001c0001t0001g0186a0001c0001t0002g0077 | 2 | NA18978.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACATATA others(5): Show |
2 | a0001c0001t0001g0078a0007c0009t0001g0166 | 2 | HG01071.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACATATA others(7): Show |
1 | a0001c0001t0001g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACATATA others(9): Show |
3 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0002g0089 | 3 | HG04204.hp2 NA18956.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CACATATA others(11): Show |
3 | a0001c0001t0001g0165a0001c0001t0002g0082a0001c0001t0007g0151 | 3 | HG01346.hp1 HG03195.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CAT | 4 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0153others(1): Show | 4 | HG01243.hp1 HG01515.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-948_1264-947d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATACATA others(3): Show |
1 | a0001c0001t0002g0083 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1264-999_1264-998i others(12): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATAT | 4 | a0001c0001t0001g0121a0001c0001t0001g0154a0001c0001t0001g0216others(1): Show | 4 | HG02809.hp2 NA18972.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-950_1264-947d others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATAT | 7 | a0001c0001t0001g0008a0001c0001t0001g0140a0001c0001t0001g0148others(4): Show | 8 | HG01123.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-952_1264-947d others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(3): Show |
4 | a0001c0001t0001g0135a0001c0001t0002g0104a0001c0001t0002g0127others(1): Show | 4 | HG01433.hp1 HG02040.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-956_1264-947d others(12): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(5): Show |
10 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0103others(7): Show | 10 | HG00738.hp2 HG01257.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1264-958_1264-947d others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(7): Show |
5 | a0001c0001t0001g0106a0001c0001t0002g0071a0001c0001t0002g0162others(2): Show | 5 | HG00140.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264-960_1264-947d others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(9): Show |
5 | a0001c0001t0001g0120a0001c0001t0002g0076a0001c0001t0024g0090others(2): Show | 5 | HG02027.hp1 HG02559.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-962_1264-947d others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(11): Show |
4 | a0001c0001t0001g0122a0001c0001t0002g0094a0001c0001t0007g0105others(1): Show | 4 | HG01081.hp1 HG01175.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-964_1264-947d others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(13): Show |
9 | a0001c0001t0001g0107a0001c0001t0001g0182a0001c0001t0001g0189others(6): Show | 9 | HG00544.hp1 HG00544.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1264-966_1264-947d others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(15): Show |
1 | a0001c0001t0001g0217 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1264-968_1264-947d others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(17): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0207a0001c0001t0007g0160 | 3 | HG02622.hp1 NA18943.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1264-970_1264-947d others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(21): Show |
1 | a0001c0001t0002g0075 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1264-974_1264-947d others(30): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
C | CATATATA others(27): Show |
1 | a0001c0001t0002g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1264-980_1264-947d others(36): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CAT | C | 5 | a0001c0001t0001g0146a0001c0001t0002g0109a0001c0001t0002g0210others(2): Show | 5 | HG01109.hp2 HG02074.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264-948_1264-947d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATAT | C | 10 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0137others(7): Show | 10 | HG00438.hp1 HG00741.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-950_1264-947d others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATAT | C | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0149others(3): Show | 6 | HG02145.hp2 HG02148.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264-952_1264-947d others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG00099.hp2 HG01496.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264-954_1264-947d others(10): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(3): Show |
C | 3 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0002g0092 | 3 | HG02486.hp1 HG03130.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1264-956_1264-947d others(12): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1264-958_1264-947d others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0002g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1264-960_1264-947d others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0002g0066a0001c0001t0002g0091 | 2 | HG00099.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1264-962_1264-947d others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(13): Show |
C | 3 | a0001c0001t0001g0187a0001c0001t0002g0074a0001c0001t0002g0112 | 3 | HG01978.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1264-966_1264-947d others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0009a0001c0001t0001g0098 | 3 | HG01496.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1264-968_1264-947d others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(23): Show |
C | 1 | a0001c0001t0012g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1264-976_1264-947d others(32): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(25): Show |
C | 4 | a0001c0001t0002g0113a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-978_1264-947d others(34): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917611
|
CATATATA others(33): Show |
C | 1 | a0001c0001t0001g0080 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1264-986_1264-947d others(42): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | |||||
chr1:108917613
|
T | C | 4 | a0001c0001t0001g0101a0001c0001t0001g0130a0001c0001t0001g0180others(1): Show | 4 | HG00408.hp1 HG02040.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1000T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917613 | ||||||
chr1:108917615
|
T | C | 6 | a0001c0001t0001g0101a0001c0001t0001g0146a0001c0001t0002g0109others(3): Show | 6 | HG01109.hp2 HG02074.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264-998T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917615 | ||||||
chr1:108917617
|
T | C | 10 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0137others(7): Show | 10 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-996T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917617 | ||||||
chr1:108917619
|
T | C | 8 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0145others(5): Show | 8 | HG00438.hp1 HG01109.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-994T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917619 | ||||||
chr1:108917621
|
T | C | 8 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0164others(5): Show | 8 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-992T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917621 | ||||||
chr1:108917623
|
T | C | 5 | a0001c0001t0001g0164a0001c0001t0001g0171a0001c0001t0001g0172others(2): Show | 5 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-990T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917623 | ||||||
chr1:108917629
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1264-984T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917629 | ||||||
chr1:108917631
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1264-982T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917631 | ||||||
chr1:108917633
|
T | C | 2 | a0001c0001t0002g0074a0001c0001t0002g0091 | 2 | NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1264-980T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917633 | ||||||
chr1:108917635
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1264-978T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917635 | ||||||
chr1:108917645
|
T | C | 1 | a0001c0001t0012g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1264-968T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917645 | ||||||
chr1:108917647
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1264-951_1264-950i others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917647 | |||||
chr1:108917663
|
T | A | 17 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(14): Show | 19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1264-950T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917663 | ||||||
chr1:108917665
|
T | A | 78 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(75): Show | 85 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(82): Show |
intron_variant | MODIFIER | c.1264-948T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917665 | ||||||
chr1:108917666
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1264-947_1264-946i others(19): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917666 | ||||||
chr1:108917667
|
A | T | 1 | a0001c0001t0002g0104 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1264-946A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917667 | ||||||
chr1:108917691
|
G | A | 8 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(5): Show | 8 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-922G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917691 | ||||||
chr1:108917830
|
TG | T | 4 | a0002c0002t0018g0016a0006c0008t0018g0018a0006c0008t0018g0218others(1): Show | 4 | HG01109.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-779delG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917830 | |||||
chr1:108917960
|
A | G | 11 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(8): Show | 11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1264-653A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917960 | ||||||
chr1:108918160
|
A | C | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264-453A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918160 | ||||||
chr1:108918186
|
G | A | 27 | a0002c0002t0020g0003a0002c0002t0020g0039a0002c0005t0008g0005others(24): Show | 29 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264-427G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918186 | ||||||
chr1:108918214
|
A | T | 1 | a0002c0002t0006g0031 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1264-399A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918214 | ||||||
chr1:108918215
|
T | A | 1 | a0002c0002t0006g0031 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1264-398T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918215 | ||||||
chr1:108918220
|
T | A | 1 | a0002c0002t0006g0031 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1264-393T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918220 | ||||||
chr1:108918341
|
C | T | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1264-272C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918341 | ||||||
chr1:108918487
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1264-126T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918487 | ||||||
chr1:108918509
|
A | G | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264-104A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918509 | ||||||
chr1:108918510
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1264-103A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918510 | ||||||
chr1:108918882
|
G | A | 1 | a0002c0002t0020g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1440+93G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108918882 | ||||||
chr1:108918911
|
A | C | 1 | a0003c0003t0047g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1440+122A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108918911 | ||||||
chr1:108919056
|
G | A | 1 | a0004c0004t0033g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1440+267G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919056 | ||||||
chr1:108919136
|
T | C | 1 | a0002c0002t0020g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1440+347T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919136 | ||||||
chr1:108919196
|
C | T | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1440+407C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919196 | ||||||
chr1:108919210
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1440+421G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919210 | ||||||
chr1:108919423
|
C | G | 6 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(3): Show | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+634C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919423 | ||||||
chr1:108919511
|
T | C | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1440+722T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919511 | ||||||
chr1:108919817
|
C | T | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1440+1028C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919817 | ||||||
chr1:108919938
|
G | A | 7 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(4): Show | 10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1440+1149G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919938 | ||||||
chr1:108919950
|
G | C | 92 | a0001c0001t0001g0188a0002c0002t0002g0024a0002c0002t0005g0012others(89): Show | 100 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(97): Show |
intron_variant | MODIFIER | c.1440+1161G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919950 | ||||||
chr1:108920123
|
C | T | 6 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(3): Show | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+1334C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920123 | ||||||
chr1:108920168
|
A | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1440+1379A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920168 | ||||||
chr1:108920186
|
T | C | 3 | a0002c0002t0009g0033a0002c0002t0009g0040a0002c0002t0009g0041 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1440+1397T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920186 | ||||||
chr1:108920228
|
G | T | 6 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(3): Show | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+1439G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920228 | ||||||
chr1:108920382
|
T | C | 1 | a0002c0002t0045g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1440+1593T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920382 | ||||||
chr1:108920458
|
G | A | 1 | a0004c0004t0031g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1440+1669G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920458 | ||||||
chr1:108920622
|
C | T | 1 | a0004c0004t0004g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1441-1795C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920622 | ||||||
chr1:108920951
|
T | A | 17 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(14): Show | 19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1441-1466T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920951 | ||||||
chr1:108920994
|
G | A | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1441-1423G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920994 | ||||||
chr1:108921052
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1441-1365C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921052 | ||||||
chr1:108921084
|
A | T | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-1333A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921084 | ||||||
chr1:108921240
|
C | T | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-1177C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921240 | ||||||
chr1:108921256
|
T | C | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-1161T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921256 | ||||||
chr1:108921416
|
CA | C | 151 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1441-986delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108921416 | |||||
chr1:108921416
|
CAA | C | 13 | a0001c0001t0001g0008a0001c0001t0002g0077a0002c0002t0009g0033others(10): Show | 14 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1441-987_1441-986d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108921416 | |||||
chr1:108921416
|
CAAA | C | 80 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(77): Show | 88 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(85): Show |
intron_variant | MODIFIER | c.1441-988_1441-986d others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108921416 | |||||
chr1:108921606
|
C | G | 27 | a0002c0002t0020g0003a0002c0002t0020g0039a0002c0005t0008g0005others(24): Show | 29 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1441-811C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921606 | ||||||
chr1:108921653
|
A | C | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-764A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921653 | ||||||
chr1:108921660
|
T | C | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1441-757T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921660 | ||||||
chr1:108921725
|
T | G | 5 | a0002c0002t0018g0016a0002c0002t0045g0019a0006c0008t0018g0018others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-692T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921725 | ||||||
chr1:108922005
|
T | TA | 36 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(33): Show | 39 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(36): Show |
intron_variant | MODIFIER | c.1441-404dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108922005 | |||||
chr1:108922043
|
A | G | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-374A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108922043 | ||||||
chr1:108922060
|
T | TAGAC | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-355_1441-354i others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108922060 | |||||
chr1:108922077
|
T | G | 4 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-340T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108922077 | ||||||
chr1:108922121
|
A | G | 6 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(3): Show | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1441-296A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108922121 | ||||||
chr1:108922692
|
GTA | G | 13 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(10): Show | 15 | HG02886.hp1 HG02970.hp1 HG03098.hp2 others(12): Show |
intron_variant | MODIFIER | c.1600+120_1600+121d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 108922692 | |||||
chr1:108922772
|
A | G | 1 | a0004c0004t0013g0001 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1600+196A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922772 | ||||||
chr1:108922842
|
A | G | 1 | a0004c0004t0004g0196 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1600+266A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922842 | ||||||
chr1:108922877
|
C | T | 1 | a0001c0014t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1600+301C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922877 | ||||||
chr1:108922879
|
C | T | 1 | a0001c0014t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1600+303C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922879 | ||||||
chr1:108923253
|
T | C | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1600+677T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923253 | ||||||
chr1:108923259
|
C | T | 1 | a0004c0004t0031g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1600+683C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923259 | ||||||
chr1:108923304
|
T | C | 1 | a0004c0004t0033g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1601-696T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923304 | ||||||
chr1:108923376
|
T | TGTA | 17 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(14): Show | 19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1601-624_1601-623i others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923376 | ||||||
chr1:108923377
|
A | T | 17 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(14): Show | 19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1601-623A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923377 | ||||||
chr1:108923441
|
A | C | 7 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(4): Show | 10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1601-559A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923441 | ||||||
chr1:108923464
|
TGGCTAAG others(5): Show |
T | 76 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(73): Show | 84 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1601-526_1601-515d others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 108923464 | |||||
chr1:108923734
|
G | C | 1 | a0001c0001t0002g0066 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1601-266G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923734 | ||||||
chr1:108923940
|
TTTTTTTG | T | 19 | a0003c0003t0003g0230a0003c0003t0003g0232a0003c0003t0003g0233others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1601-39_1601-33del others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 108923940 | |||||
chr1:108923975
|
T | C | 12 | a0004c0004t0004g0011a0004c0004t0004g0193a0004c0004t0004g0194others(9): Show | 14 | HG02886.hp1 HG02970.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.1601-25T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923975 | ||||||
chr1:108924236
|
G | A | 75 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(72): Show | 83 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1815+22G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924236 | ||||||
chr1:108924360
|
G | A | 15 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(12): Show | 15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1815+146G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924360 | ||||||
chr1:108924447
|
G | A | 22 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(19): Show | 25 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1815+233G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924447 | ||||||
chr1:108924456
|
T | G | 1 | a0002c0002t0006g0031 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1815+242T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924456 | ||||||
chr1:108924458
|
G | T | 25 | a0001c0001t0001g0155a0001c0001t0001g0168a0002c0002t0011g0044others(22): Show | 27 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1815+244G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924458 | ||||||
chr1:108924548
|
G | A | 2 | a0001c0001t0023g0049a0001c0001t0023g0050 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1815+334G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924548 | ||||||
chr1:108924651
|
G | T | 11 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(8): Show | 11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1815+437G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924651 | ||||||
chr1:108924956
|
T | C | 3 | a0004c0004t0022g0063a0004c0004t0022g0064a0004c0004t0034g0032 | 3 | HG02615.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1815+742T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924956 | ||||||
chr1:108924990
|
A | G | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1815+776A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924990 | ||||||
chr1:108925044
|
T | C | 1 | a0004c0004t0034g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1815+830T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925044 | ||||||
chr1:108925239
|
T | C | 4 | a0002c0002t0018g0016a0006c0008t0018g0018a0006c0008t0018g0218others(1): Show | 4 | HG01109.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+1025T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925239 | ||||||
chr1:108925378
|
T | C | 1 | a0002c0002t0045g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1815+1164T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925378 | ||||||
chr1:108925392
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1815+1178G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925392 | ||||||
chr1:108925498
|
C | G | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1815+1284C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925498 | ||||||
chr1:108925624
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1815+1410C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925624 | ||||||
chr1:108925785
|
G | T | 5 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+1571G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925785 | ||||||
chr1:108925824
|
G | T | 1 | a0001c0001t0001g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1815+1610G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925824 | ||||||
chr1:108925824
|
GT | G | 5 | a0001c0001t0001g0189a0001c0001t0002g0071a0002c0006t0010g0004others(2): Show | 6 | HG01081.hp2 HG01884.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1815+1621delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108925824 | |||||
chr1:108925866
|
C | A | 1 | a0004c0004t0031g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1815+1652C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925866 | ||||||
chr1:108925878
|
G | A | 1 | a0002c0010t0032g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1815+1664G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925878 | ||||||
chr1:108926031
|
G | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0104 | 2 | NA18747.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1815+1817G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926031 | ||||||
chr1:108926086
|
G | A | 75 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(72): Show | 83 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1815+1872G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926086 | ||||||
chr1:108926202
|
C | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 65 | HG00408.hp2 HG00544.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1815+1988C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926202 | ||||||
chr1:108926577
|
G | C | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1815+2363G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926577 | ||||||
chr1:108926685
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1815+2471G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926685 | ||||||
chr1:108926692
|
A | C | 27 | a0002c0002t0020g0003a0002c0002t0020g0039a0002c0005t0008g0005others(24): Show | 29 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1815+2478A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926692 | ||||||
chr1:108926709
|
A | G | 19 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(16): Show | 22 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1815+2495A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926709 | ||||||
chr1:108926714
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1815+2500G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926714 | ||||||
chr1:108926947
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1815+2733A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926947 | ||||||
chr1:108927301
|
A | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0215 | 2 | NA19000.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1816-2400A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927301 | ||||||
chr1:108927311
|
T | C | 7 | a0002c0002t0005g0012a0002c0002t0005g0013a0002c0002t0005g0014others(4): Show | 10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1816-2390T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927311 | ||||||
chr1:108927459
|
T | C | 1 | a0001c0001t0046g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1816-2242T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927459 | ||||||
chr1:108927504
|
A | G | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2197A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927504 | ||||||
chr1:108927563
|
T | C | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2138T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927563 | ||||||
chr1:108927624
|
C | T | 2 | a0002c0002t0006g0031a0008c0011t0006g0025 | 2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1816-2077C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927624 | ||||||
chr1:108927646
|
G | A | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2055G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927646 | ||||||
chr1:108927647
|
C | T | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2054C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927647 | ||||||
chr1:108927813
|
A | T | 1 | a0002c0006t0010g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1816-1888A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927813 | ||||||
chr1:108927977
|
A | G | 2 | a0004c0004t0022g0063a0004c0004t0022g0064 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1816-1724A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927977 | ||||||
chr1:108928038
|
G | A | 91 | a0002c0002t0002g0024a0002c0002t0005g0012a0002c0002t0005g0013others(88): Show | 99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-1663G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928038 | ||||||
chr1:108928303
|
T | C | 10 | a0002c0002t0011g0044a0002c0002t0011g0045a0002c0002t0011g0046others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1816-1398T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928303 | ||||||
chr1:108928398
|
T | TGGA | 11 | a0002c0002t0009g0033a0002c0002t0009g0036a0002c0002t0009g0038others(8): Show | 11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1816-1299_1816-129 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108928398 | |||||
chr1:108928477
|
G | A | 1 | a0002c0005t0008g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1816-1224G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928477 | ||||||
chr1:108928847
|
A | G | 123 | a0001c0001t0002g0006a0001c0001t0002g0015a0001c0001t0002g0066others(120): Show | 129 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1816-854A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928847 | ||||||
chr1:108928867
|
A | G | 237 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(234): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1816-834A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928867 | ||||||
chr1:108928986
|
C | T | 59 | a0001c0001t0002g0006a0001c0001t0002g0015a0001c0001t0002g0066others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1816-715C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928986 | ||||||
chr1:108928988
|
C | CA | 18 | a0001c0001t0001g0165a0001c0001t0001g0184a0002c0005t0014g0062others(15): Show | 20 | HG01346.hp1 HG01891.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1816-694dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108928988 | |||||
chr1:108928988
|
CA | C | 66 | a0001c0001t0001g0129a0001c0001t0001g0147a0001c0001t0001g0186others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1816-694delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108928988 | |||||
chr1:108929012
|
T | G | 133 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0002g0006others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1816-689T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929012 | ||||||
chr1:108929023
|
TTC | T | 59 | a0001c0001t0002g0006a0001c0001t0002g0015a0001c0001t0002g0066others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1816-676_1816-675d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108929023 | |||||
chr1:108929107
|
G | A | 16 | a0002c0002t0002g0024a0002c0002t0006g0002a0002c0002t0006g0023others(13): Show | 16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1816-594G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929107 | ||||||
chr1:108929227
|
G | A | 3 | a0002c0006t0010g0004a0002c0006t0010g0020a0002c0006t0010g0021 | 4 | HG01884.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-474G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929227 | ||||||
chr1:108929298
|
G | C | 61 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0002g0006others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1816-403G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929298 | ||||||
chr1:108929670
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1816-31A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929670 | ||||||
chr1:108929693
|
A | G | 3 | a0002c0002t0019g0034a0002c0002t0019g0035a0002c0002t0019g0037 | 3 | HG01099.hp1 HG02965.hp1 HG03540.hp1 |
splice_region_variant&intron_variant | LOW | c.1816-8A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929693 |