geneid | 5707 |
---|---|
ensemblid | ENSG00000173692.14 |
hgncid | 9554 |
symbol | PSMD1 |
name | proteasome 26S subunit, non-ATPase 1 |
refseq_nuc | NM_002807.4 |
refseq_prot | NP_002798.2 |
ensembl_nuc | ENST00000308696.11 |
ensembl_prot | ENSP00000309474.6 |
mane_status | MANE Select |
chr | chr2 |
start | 231056867 |
end | 231172827 |
strand | + |
ver | v1.2 |
region | chr2:231056867-231172827 |
region5000 | chr2:231051867-231177827 |
regionname0 | PSMD1_chr2_231056867_231172827 |
regionname5000 | PSMD1_chr2_231051867_231177827 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 953 | 360 | 85 | 48 | 179 | 10 | 36 | 144 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0002 | 0/0 | 953 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0003 | 0/0 | 953 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0004 | 0/0 | 953 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2862 | 353 | 78 | 48 | 179 | 10 | 36 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
c0002 | 0/0 | 2862 | 5 | 5 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
c0003 | 0/0 | 2862 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
c0004 | 0/0 | 2862 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
c0005 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
c0006 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
c0007 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 462 | 194 | 44 | 22 | 111 | 2 | 15 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
t0002 | 1/1 | 462 | 104 | 9 | 21 | 53 | 4 | 15 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
t0003 | 0/0 | 462 | 58 | 27 | 5 | 17 | 4 | 5 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
t0004 | 0/0 | 462 | 5 | 5 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
t0005 | 0/0 | 462 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
t0006 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
t0007 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2862 | 353 | 78 | 48 | 179 | 10 | 36 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0002 | 0/0 | 2862 | 5 | 5 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0005 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0006 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0002c0003 | 0/0 | 2862 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0003c0007 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0004c0004 | 0/0 | 2862 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3323 | 192 | 42 | 22 | 111 | 2 | 15 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0001t0002 | 1/1 | 3323 | 101 | 8 | 21 | 51 | 4 | 15 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0001t0003 | 0/0 | 3323 | 57 | 27 | 5 | 16 | 4 | 5 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0001t0005 | 0/0 | 3323 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0001t0006 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0001t0007 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0002t0004 | 0/0 | 3323 | 5 | 5 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0005t0001 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0001c0006t0002 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0002c0003t0002 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0002c0003t0003 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0003c0007t0001 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
a0004c0004t0002 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | copy fasta | chr2 | 231051867 | 231177827 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0001c0006t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0003c0007t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
a0004c0004t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0003 | g0144 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0347 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0161 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0159 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0145 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01891 | hp1 | a0003 | c0007 | t0001 | g0238 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02129 | hp1 | a0002 | c0003 | t0003 | g0155 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0352 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02280 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02280 | hp2 | a0001 | c0006 | t0002 | g0106 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0063 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0354 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0344 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0026 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0337 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0338 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0120 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03579 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0353 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0140 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19003 | hp1 | a0004 | c0004 | t0002 | g0009 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19088 | hp1 | a0002 | c0003 | t0002 | g0079 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0355 | AFR | ASW | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | TSI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | GIH | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | GIH | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20300 | hp1 | a0001 | c0005 | t0001 | g0028 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0097 | REF | REF | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0030 | REF | REF | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231067085
|
G | A | 1 | a0002 | 2 | HG02129.hp1 NA19088.hp1 |
missense_variant | MODERATE | c.484G>A | p.Val162Ile | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/25 | 643/3323 | 484/2862 | 162/953 | chr2 | 231067085 | ||
chr2:231067092
|
A | C | 1 | a0003 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.491A>C | p.Glu164Ala | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/25 | 650/3323 | 491/2862 | 164/953 | chr2 | 231067092 | ||
chr2:231153639
|
A | G | 1 | a0004 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.2191A>G | p.Ile731Val | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/25 | 2350/3323 | 2191/2862 | 731/953 | chr2 | 231153639 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231070117
|
A | G | 1 | a0001c0006 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.603A>G | p.Leu201Leu | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/25 | 762/3323 | 603/2862 | 201/953 | chr2 | 231070117 | ||
chr2:231072269
|
A | G | 1 | a0001c0005 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.735A>G | p.Ala245Ala | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/25 | 894/3323 | 735/2862 | 245/953 | chr2 | 231072269 | ||
chr2:231163682
|
A | G | 1 | a0001c0002 | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.2436A>G | p.Ala812Ala | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/25 | 2595/3323 | 2436/2862 | 812/953 | chr2 | 231163682 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231056872
|
G | C | 3 | a0001c0001t0003a0001c0001t0005a0002c0003t0003 | 59 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-154G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/25 | 154 | chr2 | 231056872 | |||||
chr2:231056930
|
C | A | 1 | a0001c0001t0006 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/25 | 96 | chr2 | 231056930 | |||||
chr2:231056955
|
C | G | 1 | a0001c0002t0004 | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-71C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/25 | 71 | chr2 | 231056955 | |||||
chr2:231170715
|
G | A | 8 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(5): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/25 | 3 | chr2 | 231170715 | |||||
chr2:231172709
|
C | G | 1 | a0001c0001t0005 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 25/25 | 1997 | chr2 | 231172709 | |||||
chr2:231172803
|
C | T | 1 | a0001c0001t0007 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 25/25 | 2091 | chr2 | 231172803 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231057179
|
C | T | 2 | a0001c0001t0003g0354a0001c0001t0003g0355 | 2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.16+138C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057179 | ||||||
chr2:231057232
|
G | C | 12 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(9): Show | 12 | HG01346.hp2 HG03654.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.16+191G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057232 | ||||||
chr2:231057236
|
A | G | 1 | a0001c0001t0002g0353 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16+195A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057236 | ||||||
chr2:231057272
|
A | G | 1 | a0001c0001t0002g0352 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.16+231A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057272 | ||||||
chr2:231057548
|
A | G | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+507A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057548 | ||||||
chr2:231057654
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.16+613C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057654 | ||||||
chr2:231058123
|
A | G | 1 | a0001c0001t0002g0345 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.16+1082A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058123 | ||||||
chr2:231058285
|
T | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16+1244T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058285 | ||||||
chr2:231058339
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.16+1298C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058339 | ||||||
chr2:231058520
|
CT | C | 57 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0130others(54): Show | 59 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.16+1494delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231058520 | |||||
chr2:231058626
|
C | T | 4 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+1585C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058626 | ||||||
chr2:231058716
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.16+1675T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058716 | ||||||
chr2:231058825
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0003g0344 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.16+1784C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058825 | ||||||
chr2:231058845
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.16+1804T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058845 | ||||||
chr2:231058912
|
A | C | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.16+1871A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058912 | ||||||
chr2:231058952
|
G | GTC | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(48): Show | 53 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.16+1927_16+1928dup others(2): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231058952 | |||||
chr2:231059025
|
A | G | 32 | a0001c0001t0003g0004a0001c0001t0003g0133a0001c0001t0003g0134others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.16+1984A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059025 | ||||||
chr2:231059220
|
T | C | 1 | a0001c0002t0004g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.17-2047T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059220 | ||||||
chr2:231059223
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.17-2044A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059223 | ||||||
chr2:231059235
|
G | T | 1 | a0001c0001t0001g0341 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.17-2032G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059235 | ||||||
chr2:231059493
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0210a0001c0001t0001g0211others(15): Show | 19 | HG02683.hp2 HG03490.hp2 HG03491.hp1 others(16): Show |
intron_variant | MODIFIER | c.17-1774G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059493 | ||||||
chr2:231059501
|
G | A | 2 | a0001c0001t0003g0133a0001c0001t0003g0134 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.17-1766G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059501 | ||||||
chr2:231059574
|
A | C | 1 | a0001c0001t0001g0340 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.17-1693A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059574 | ||||||
chr2:231059651
|
C | T | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17-1616C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059651 | ||||||
chr2:231060153
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.17-1114G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060153 | ||||||
chr2:231060326
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.17-941A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060326 | ||||||
chr2:231060450
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.17-817C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060450 | ||||||
chr2:231060933
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.17-334C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060933 | ||||||
chr2:231060952
|
T | A | 1 | a0001c0001t0003g0135 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.17-315T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060952 | ||||||
chr2:231061020
|
A | C | 354 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 363 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(360): Show |
intron_variant | MODIFIER | c.17-247A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061020 | ||||||
chr2:231061035
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.17-232T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061035 | ||||||
chr2:231061162
|
C | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.17-105C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061162 | ||||||
chr2:231061175
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.17-92G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061175 | ||||||
chr2:231061218
|
C | T | 4 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0337others(1): Show | 4 | HG02145.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-49C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061218 | ||||||
chr2:231061606
|
C | G | 1 | a0001c0001t0002g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.60+296C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061606 | ||||||
chr2:231061869
|
G | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0032 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.61-379G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061869 | ||||||
chr2:231061877
|
C | T | 1 | a0001c0001t0002g0353 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61-371C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061877 | ||||||
chr2:231061896
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.61-352A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061896 | ||||||
chr2:231061978
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.61-270G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061978 | ||||||
chr2:231062106
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61-142T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231062106 | ||||||
chr2:231062235
|
T | C | 6 | a0001c0001t0003g0004a0001c0001t0003g0136a0001c0001t0003g0137others(3): Show | 7 | HG03834.hp2 NA18963.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-13T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231062235 | ||||||
chr2:231062690
|
T | A | 2 | a0001c0001t0001g0343a0001c0001t0003g0344 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.304+15T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062690 | ||||||
chr2:231062855
|
G | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.304+180G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062855 | ||||||
chr2:231062856
|
G | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.304+181G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062856 | ||||||
chr2:231062951
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.304+276G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062951 | ||||||
chr2:231063067
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.304+392A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063067 | ||||||
chr2:231063178
|
T | C | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.304+503T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063178 | ||||||
chr2:231063191
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0002g0033 | 2 | HG02258.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.304+516G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063191 | ||||||
chr2:231063343
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.304+668G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063343 | ||||||
chr2:231063396
|
T | C | 1 | a0001c0001t0002g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.304+721T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063396 | ||||||
chr2:231063497
|
G | A | 1 | a0001c0001t0003g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.304+822G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063497 | ||||||
chr2:231063561
|
T | A | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.304+886T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063561 | ||||||
chr2:231063594
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.304+919G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063594 | ||||||
chr2:231063828
|
AT | A | 351 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(348): Show | 360 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.304+1166delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231063828 | |||||
chr2:231064261
|
T | A | 1 | a0001c0001t0001g0289 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.304+1586T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064261 | ||||||
chr2:231064302
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+1627A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064302 | ||||||
chr2:231064324
|
C | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304+1649C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064324 | ||||||
chr2:231064463
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.304+1788A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064463 | ||||||
chr2:231064916
|
CT | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.305-1988delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231064916 | |||||
chr2:231064947
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0339 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.305-1959C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064947 | ||||||
chr2:231065002
|
A | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG03927.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.305-1904A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065002 | ||||||
chr2:231065052
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.305-1854C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065052 | ||||||
chr2:231065063
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.305-1843A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065063 | ||||||
chr2:231065177
|
A | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.305-1729A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065177 | ||||||
chr2:231065226
|
A | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1680A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065226 | ||||||
chr2:231065261
|
G | GTTTTTTG others(1): Show |
5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1630_305-1623d others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065261 | |||||
chr2:231065261
|
G | GTTTTTTG others(10): Show |
1 | a0001c0001t0003g0162 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.305-1622_305-1606d others(19): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065261 | |||||
chr2:231065354
|
G | A | 6 | a0001c0001t0001g0022a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-1552G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065354 | ||||||
chr2:231065421
|
T | A | 56 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0117others(53): Show | 58 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.305-1485T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065421 | ||||||
chr2:231065459
|
A | ATT | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0002t0004g0023others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.305-1435_305-1434d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065459 | |||||
chr2:231065459
|
A | ATTT | 176 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.305-1436_305-1434d others(5): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065459 | |||||
chr2:231065459
|
A | ATTTT | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(63): Show | 68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.305-1437_305-1434d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065459 | |||||
chr2:231065497
|
C | A | 1 | a0001c0001t0001g0289 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.305-1409C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065497 | ||||||
chr2:231065501
|
G | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.305-1405G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065501 | ||||||
chr2:231065591
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.305-1315G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065591 | ||||||
chr2:231065835
|
C | T | 11 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(8): Show | 11 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.305-1071C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065835 | ||||||
chr2:231065852
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.305-1054G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065852 | ||||||
chr2:231065968
|
C | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.305-938C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065968 | ||||||
chr2:231066206
|
A | G | 1 | a0001c0001t0003g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.305-700A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066206 | ||||||
chr2:231066419
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.305-487T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066419 | ||||||
chr2:231066502
|
G | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.305-404G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066502 | ||||||
chr2:231066609
|
G | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.305-297G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066609 | ||||||
chr2:231066638
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0334a0001c0001t0001g0335others(1): Show | 5 | HG00438.hp1 HG00558.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-268C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066638 | ||||||
chr2:231066657
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.305-249G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066657 | ||||||
chr2:231066668
|
C | T | 2 | a0001c0001t0003g0164a0001c0001t0003g0167 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.305-238C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066668 | ||||||
chr2:231067349
|
T | C | 9 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(6): Show | 9 | NA18948.hp1 NA18960.hp1 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+238T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067349 | ||||||
chr2:231067420
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.510+309T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067420 | ||||||
chr2:231067533
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510+422A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067533 | ||||||
chr2:231067657
|
T | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+546T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067657 | ||||||
chr2:231067802
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.510+691G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067802 | ||||||
chr2:231067846
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.510+735G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067846 | ||||||
chr2:231068201
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510+1090A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068201 | ||||||
chr2:231068372
|
C | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.510+1261C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068372 | ||||||
chr2:231068373
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+1262G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068373 | ||||||
chr2:231068547
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(72): Show | 77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.510+1436A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068547 | ||||||
chr2:231068686
|
A | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.511-1339A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068686 | ||||||
chr2:231068694
|
C | T | 2 | a0001c0001t0002g0111a0001c0001t0002g0116 | 2 | HG01081.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.511-1331C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068694 | ||||||
chr2:231068944
|
A | G | 7 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-1081A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068944 | ||||||
chr2:231069089
|
C | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.511-936C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069089 | ||||||
chr2:231069188
|
T | A | 1 | a0001c0001t0002g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.511-837T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069188 | ||||||
chr2:231069188
|
T | TA | 7 | a0001c0001t0001g0232a0001c0001t0001g0284a0001c0001t0001g0291others(4): Show | 7 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-825dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231069188 | |||||
chr2:231069189
|
A | T | 5 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0285others(2): Show | 5 | HG02155.hp1 NA18964.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-836A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069189 | ||||||
chr2:231069998
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.511-27G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069998 | ||||||
chr2:231070215
|
G | A | 3 | a0001c0002t0004g0024a0001c0002t0004g0025a0001c0002t0004g0026 | 3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.654+47G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070215 | ||||||
chr2:231070245
|
A | G | 1 | a0001c0001t0003g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.654+77A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070245 | ||||||
chr2:231070252
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.654+84A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070252 | ||||||
chr2:231070277
|
A | G | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG01243.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.654+109A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070277 | ||||||
chr2:231070484
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.654+316A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070484 | ||||||
chr2:231070495
|
A | G | 7 | a0001c0001t0001g0227a0001c0001t0001g0328a0001c0001t0001g0329others(4): Show | 7 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+327A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070495 | ||||||
chr2:231070527
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.654+359A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070527 | ||||||
chr2:231070562
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.654+394C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070562 | ||||||
chr2:231070611
|
T | G | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.654+443T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070611 | ||||||
chr2:231070885
|
G | C | 4 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(1): Show | 4 | HG02027.hp1 NA18947.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+717G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070885 | ||||||
chr2:231070962
|
C | T | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | HG00408.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.654+794C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070962 | ||||||
chr2:231071093
|
G | T | 1 | a0001c0001t0003g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.654+925G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071093 | ||||||
chr2:231071104
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | NA18966.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.654+936C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071104 | ||||||
chr2:231071204
|
C | T | 39 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0121others(36): Show | 41 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.655-985C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071204 | ||||||
chr2:231071325
|
G | A | 11 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(8): Show | 11 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.655-864G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071325 | ||||||
chr2:231071615
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.655-574A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071615 | ||||||
chr2:231071655
|
A | T | 1 | a0001c0001t0002g0109 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.655-534A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071655 | ||||||
chr2:231071660
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-529G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071660 | ||||||
chr2:231071770
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655-419T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071770 | ||||||
chr2:231071917
|
C | A | 3 | a0001c0002t0004g0024a0001c0002t0004g0025a0001c0002t0004g0026 | 3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.655-272C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071917 | ||||||
chr2:231072536
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.881+121T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072536 | ||||||
chr2:231072605
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.881+190T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072605 | ||||||
chr2:231072791
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.881+376A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072791 | ||||||
chr2:231072825
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.881+410T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072825 | ||||||
chr2:231072893
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG00733.hp2 HG01081.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.881+478C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072893 | ||||||
chr2:231072899
|
G | A | 3 | a0001c0002t0004g0024a0001c0002t0004g0025a0001c0002t0004g0026 | 3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.881+484G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072899 | ||||||
chr2:231073257
|
A | G | 1 | a0001c0001t0003g0160 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.881+842A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073257 | ||||||
chr2:231073292
|
A | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020 | 3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.881+877A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073292 | ||||||
chr2:231073332
|
A | G | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | NA18952.hp1 NA18957.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.881+917A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073332 | ||||||
chr2:231073479
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0193others(79): Show | 84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.881+1064C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073479 | ||||||
chr2:231073507
|
T | C | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+1092T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073507 | ||||||
chr2:231073558
|
G | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+1143G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073558 | ||||||
chr2:231073588
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.881+1173G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073588 | ||||||
chr2:231073621
|
G | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.881+1206G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073621 | ||||||
chr2:231073801
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.881+1386G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073801 | ||||||
chr2:231073996
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882-1515C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073996 | ||||||
chr2:231074103
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.882-1408G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074103 | ||||||
chr2:231074294
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0006g0278 | 3 | HG02451.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.882-1217C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074294 | ||||||
chr2:231074431
|
G | A | 1 | a0001c0001t0001g0346 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882-1080G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074431 | ||||||
chr2:231074700
|
T | C | 4 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-811T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074700 | ||||||
chr2:231074798
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882-713A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074798 | ||||||
chr2:231074812
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.882-699A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074812 | ||||||
chr2:231074917
|
C | T | 3 | a0001c0002t0004g0024a0001c0002t0004g0025a0001c0002t0004g0026 | 3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.882-594C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074917 | ||||||
chr2:231075253
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.882-258A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231075253 | ||||||
chr2:231075339
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.882-172A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231075339 | ||||||
chr2:231075408
|
CATT | C | 3 | a0001c0001t0001g0281a0001c0002t0004g0023a0001c0002t0004g0027 | 3 | HG02280.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882-99_882-97delAT others(1): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr2 | 231075408 | |||||
chr2:231075425
|
A | G | 3 | a0001c0002t0004g0024a0001c0002t0004g0025a0001c0002t0004g0026 | 3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.882-86A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231075425 | ||||||
chr2:231075648
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0193others(79): Show | 84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.942+77C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075648 | ||||||
chr2:231075740
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0048 | 2 | NA18968.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.942+169C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075740 | ||||||
chr2:231075789
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.942+218C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075789 | ||||||
chr2:231075872
|
C | T | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.942+301C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075872 | ||||||
chr2:231075878
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.942+307A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075878 | ||||||
chr2:231075895
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.942+324G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075895 | ||||||
chr2:231075930
|
A | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.942+359A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075930 | ||||||
chr2:231075950
|
G | A | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.942+379G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075950 | ||||||
chr2:231075957
|
C | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.942+386C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075957 | ||||||
chr2:231076149
|
A | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.942+578A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076149 | ||||||
chr2:231076162
|
A | G | 12 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 12 | HG00408.hp2 HG02015.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.942+591A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076162 | ||||||
chr2:231076246
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.942+675A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076246 | ||||||
chr2:231076305
|
G | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.943-729G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076305 | ||||||
chr2:231076416
|
C | T | 1 | a0001c0006t0002g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.943-618C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076416 | ||||||
chr2:231076538
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.943-496A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076538 | ||||||
chr2:231076540
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.943-494G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076540 | ||||||
chr2:231076570
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.943-464C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076570 | ||||||
chr2:231076904
|
GAAAT | G | 11 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(8): Show | 11 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(8): Show |
intron_variant | MODIFIER | c.943-125_943-122del others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231076904 | |||||
chr2:231076908
|
T | G | 1 | a0001c0001t0001g0334 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.943-126T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076908 | ||||||
chr2:231077016
|
T | G | 1 | a0001c0001t0005g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.943-18T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231077016 | ||||||
chr2:231077355
|
T | C | 8 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071+193T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077355 | ||||||
chr2:231077481
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1071+319G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077481 | ||||||
chr2:231077698
|
A | G | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1071+536A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077698 | ||||||
chr2:231077778
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(243): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.1071+616G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077778 | ||||||
chr2:231077810
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1071+648A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077810 | ||||||
chr2:231077962
|
T | A | 1 | a0001c0001t0001g0294 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1072-697T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077962 | ||||||
chr2:231077968
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1072-691T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077968 | ||||||
chr2:231078005
|
C | T | 2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1072-654C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078005 | ||||||
chr2:231078160
|
C | T | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1072-499C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078160 | ||||||
chr2:231078376
|
G | A | 7 | a0001c0001t0002g0010a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | NA18966.hp1 NA19003.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1072-283G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078376 | ||||||
chr2:231078426
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1072-233C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078426 | ||||||
chr2:231078631
|
T | G | 1 | a0001c0001t0003g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1072-28T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078631 | ||||||
chr2:231078791
|
C | CT | 102 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(99): Show | 104 | HG00408.hp2 HG00558.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.1160+68dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr2 | 231078791 | |||||
chr2:231078791
|
C | CTT | 13 | a0001c0001t0001g0195a0001c0001t0001g0208a0001c0001t0001g0263others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160+67_1160+68dup others(2): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr2 | 231078791 | |||||
chr2:231078791
|
CT | C | 8 | a0001c0001t0001g0335a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG00438.hp1 HG01074.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160+68delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr2 | 231078791 | |||||
chr2:231079004
|
A | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1160+257A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079004 | ||||||
chr2:231079287
|
T | C | 6 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(3): Show | 6 | NA18952.hp1 NA18957.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-249T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079287 | ||||||
chr2:231079303
|
T | G | 6 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(3): Show | 6 | NA18952.hp1 NA18957.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-233T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079303 | ||||||
chr2:231079403
|
A | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161-133A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079403 | ||||||
chr2:231079477
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1161-59A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079477 | ||||||
chr2:231079659
|
A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.1239+45A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 11/24 | chr2 | 231079659 | ||||||
chr2:231079973
|
G | C | 1 | a0001c0001t0001g0334 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240-168G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 11/24 | chr2 | 231079973 | ||||||
chr2:231080423
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1413+109A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080423 | ||||||
chr2:231080586
|
A | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(22): Show | 27 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1413+272A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080586 | ||||||
chr2:231080706
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1413+392T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080706 | ||||||
chr2:231080871
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413+557G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080871 | ||||||
chr2:231080909
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0342 | 3 | HG01070.hp2 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1413+595G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080909 | ||||||
chr2:231080964
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1413+650G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080964 | ||||||
chr2:231081004
|
C | A | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1413+690C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081004 | ||||||
chr2:231081144
|
T | TA | 11 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0199others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413+852dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | |||||
chr2:231081144
|
T | TAAAA | 8 | a0001c0001t0001g0168a0001c0001t0001g0316a0001c0001t0001g0317others(5): Show | 8 | HG02027.hp2 HG02965.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1413+849_1413+852d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | |||||
chr2:231081144
|
T | TAAAAA | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0210others(50): Show | 55 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1413+848_1413+852d others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | |||||
chr2:231081144
|
T | TAAAAAA | 11 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(8): Show | 11 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413+847_1413+852d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | |||||
chr2:231081144
|
TA | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0186a0001c0001t0001g0229others(13): Show | 16 | HG00323.hp1 HG01515.hp2 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.1413+852delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | |||||
chr2:231081170
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413+856T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081170 | ||||||
chr2:231081366
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413+1052C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081366 | ||||||
chr2:231081418
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1413+1104T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081418 | ||||||
chr2:231081518
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1413+1204G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081518 | ||||||
chr2:231081573
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1413+1259G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081573 | ||||||
chr2:231081594
|
G | C | 1 | a0001c0001t0003g0142 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1413+1280G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081594 | ||||||
chr2:231081778
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1414-1105A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081778 | ||||||
chr2:231081980
|
C | A | 1 | a0001c0001t0001g0299 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1414-903C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081980 | ||||||
chr2:231082186
|
C | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1414-697C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082186 | ||||||
chr2:231082188
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1414-695G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082188 | ||||||
chr2:231082256
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1414-627G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082256 | ||||||
chr2:231082476
|
G | A | 2 | a0001c0001t0003g0136a0001c0001t0003g0138 | 2 | NA18963.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1414-407G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082476 | ||||||
chr2:231082502
|
A | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.1414-381A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082502 | ||||||
chr2:231082506
|
A | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0353 | 3 | HG03490.hp1 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1414-377A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082506 | ||||||
chr2:231082718
|
C | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1414-165C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082718 | ||||||
chr2:231082753
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-130A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082753 | ||||||
chr2:231083054
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1525+60A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083054 | ||||||
chr2:231083066
|
C | G | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1525+72C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083066 | ||||||
chr2:231083391
|
A | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1526-176A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083391 | ||||||
chr2:231083464
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1526-103A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083464 | ||||||
chr2:231083989
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1722+226C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231083989 | ||||||
chr2:231084087
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1722+324G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084087 | ||||||
chr2:231084114
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1722+351C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084114 | ||||||
chr2:231084115
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1722+352G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084115 | ||||||
chr2:231084220
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1722+457C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084220 | ||||||
chr2:231084222
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1722+459G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084222 | ||||||
chr2:231084284
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1722+521A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084284 | ||||||
chr2:231084372
|
T | A | 1 | a0001c0001t0003g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1722+609T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084372 | ||||||
chr2:231084456
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1723-563C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084456 | ||||||
chr2:231084465
|
T | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1723-554T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084465 | ||||||
chr2:231084537
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1723-482G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084537 | ||||||
chr2:231084582
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1723-437G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084582 | ||||||
chr2:231084584
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1723-435T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084584 | ||||||
chr2:231084855
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1723-164T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084855 | ||||||
chr2:231084884
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1723-135A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084884 | ||||||
chr2:231084890
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1723-129A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084890 | ||||||
chr2:231084976
|
G | C | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1723-43G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084976 | ||||||
chr2:231085232
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1818+118G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231085232 | ||||||
chr2:231085674
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0334a0001c0001t0001g0335others(1): Show | 5 | HG00438.hp1 HG00558.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+560A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231085674 | ||||||
chr2:231086009
|
C | T | 1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1818+895C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086009 | ||||||
chr2:231086093
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1818+979C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086093 | ||||||
chr2:231086133
|
T | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038 | 3 | HG01074.hp1 HG04204.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1819-984T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086133 | ||||||
chr2:231086244
|
G | C | 1 | a0001c0001t0001g0244 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1819-873G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086244 | ||||||
chr2:231086368
|
G | T | 11 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(8): Show | 11 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(8): Show |
intron_variant | MODIFIER | c.1819-749G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086368 | ||||||
chr2:231086389
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020 | 3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1819-728G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086389 | ||||||
chr2:231086529
|
C | T | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-588C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086529 | ||||||
chr2:231086714
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1819-403G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086714 | ||||||
chr2:231087328
|
A | C | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1883+147A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087328 | ||||||
chr2:231087471
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1883+290C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087471 | ||||||
chr2:231087777
|
ACGGTGAA others(3): Show |
A | 1 | a0001c0001t0002g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1883+598_1883+607d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231087777 | |||||
chr2:231087897
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+716A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087897 | ||||||
chr2:231087927
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+746A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087927 | ||||||
chr2:231087961
|
T | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+780T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087961 | ||||||
chr2:231087968
|
A | G | 1 | a0001c0001t0001g0350 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1883+787A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087968 | ||||||
chr2:231087984
|
A | T | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+803A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087984 | ||||||
chr2:231088713
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1883+1532G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231088713 | ||||||
chr2:231088718
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+1537A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231088718 | ||||||
chr2:231089249
|
A | G | 1 | a0002c0003t0003g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1883+2068A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089249 | ||||||
chr2:231089377
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1883+2196A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089377 | ||||||
chr2:231089522
|
T | C | 11 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(8): Show | 11 | HG00438.hp2 HG00609.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.1883+2341T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089522 | ||||||
chr2:231089549
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 119 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1883+2368A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089549 | ||||||
chr2:231089594
|
G | GAT | 14 | a0001c0001t0001g0171a0001c0001t0001g0232a0001c0001t0001g0245others(11): Show | 14 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1883+2432_1883+243 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | |||||
chr2:231089594
|
G | GATATATA others(7): Show |
1 | a0001c0002t0004g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1883+2420_1883+243 others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | |||||
chr2:231089594
|
G | GATATATA others(9): Show |
1 | a0001c0002t0004g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1883+2418_1883+243 others(20): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | |||||
chr2:231089594
|
G | GATATATA others(37): Show |
1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1883+2433_1883+243 others(48): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | |||||
chr2:231089594
|
G | GATATATA others(45): Show |
1 | a0001c0002t0004g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1883+2433_1883+243 others(56): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | |||||
chr2:231089594
|
G | GATATATA others(49): Show |
1 | a0001c0002t0004g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1883+2433_1883+243 others(60): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | |||||
chr2:231089917
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+2736C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089917 | ||||||
chr2:231089924
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1883+2743A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089924 | ||||||
chr2:231090176
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1883+2995C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090176 | ||||||
chr2:231090312
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1883+3131G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090312 | ||||||
chr2:231090331
|
C | A | 56 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0117others(53): Show | 58 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1883+3150C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090331 | ||||||
chr2:231090565
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+3384A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090565 | ||||||
chr2:231090609
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1883+3428C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090609 | ||||||
chr2:231090623
|
G | T | 1 | a0001c0001t0003g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1883+3442G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090623 | ||||||
chr2:231090690
|
T | G | 7 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+3509T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090690 | ||||||
chr2:231090831
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1883+3650C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090831 | ||||||
chr2:231091195
|
G | C | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1883+4014G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091195 | ||||||
chr2:231091209
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1883+4028C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091209 | ||||||
chr2:231091772
|
C | T | 1 | a0001c0001t0003g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1883+4591C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091772 | ||||||
chr2:231091838
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+4657G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091838 | ||||||
chr2:231091903
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1883+4722C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091903 | ||||||
chr2:231092038
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1883+4857A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092038 | ||||||
chr2:231092215
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1883+5034G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092215 | ||||||
chr2:231092547
|
C | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1883+5366C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092547 | ||||||
chr2:231092579
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+5398G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092579 | ||||||
chr2:231092610
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1883+5429G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092610 | ||||||
chr2:231092616
|
C | A | 1 | a0001c0001t0005g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1883+5435C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092616 | ||||||
chr2:231092734
|
G | T | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+5553G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092734 | ||||||
chr2:231093311
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG03453.hp2 HG03471.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+6130A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093311 | ||||||
chr2:231093398
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1883+6217C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093398 | ||||||
chr2:231093401
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1883+6220G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093401 | ||||||
chr2:231093424
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1883+6243C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093424 | ||||||
chr2:231093425
|
G | A | 6 | a0001c0001t0002g0111a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG02280.hp1 HG02683.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1883+6244G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093425 | ||||||
chr2:231093433
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1883+6252C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093433 | ||||||
chr2:231093478
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1883+6297A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093478 | ||||||
chr2:231094157
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1883+6976G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094157 | ||||||
chr2:231094165
|
C | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1883+6984C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094165 | ||||||
chr2:231094200
|
A | G | 1 | a0001c0001t0002g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1883+7019A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094200 | ||||||
chr2:231094325
|
T | C | 1 | a0001c0001t0002g0352 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1883+7144T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094325 | ||||||
chr2:231094583
|
G | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+7402G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094583 | ||||||
chr2:231094681
|
G | A | 7 | a0001c0001t0001g0227a0001c0001t0001g0328a0001c0001t0001g0329others(4): Show | 7 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+7500G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094681 | ||||||
chr2:231095054
|
G | A | 7 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+7873G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095054 | ||||||
chr2:231095104
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1883+7923A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095104 | ||||||
chr2:231095111
|
T | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+7930T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095111 | ||||||
chr2:231095275
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1883+8094T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095275 | ||||||
chr2:231095584
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1883+8403G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095584 | ||||||
chr2:231095862
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+8681G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095862 | ||||||
chr2:231095864
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1883+8683C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095864 | ||||||
chr2:231095882
|
G | A | 8 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01361.hp2 NA18942.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.1883+8701G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095882 | ||||||
chr2:231095910
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1883+8729A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095910 | ||||||
chr2:231096028
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1883+8847A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096028 | ||||||
chr2:231096127
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+8946T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096127 | ||||||
chr2:231096192
|
A | G | 2 | a0001c0001t0003g0164a0001c0001t0003g0167 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1883+9011A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096192 | ||||||
chr2:231096455
|
G | C | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+9274G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096455 | ||||||
chr2:231096480
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0178a0001c0001t0001g0179others(8): Show | 12 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1883+9299C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096480 | ||||||
chr2:231096569
|
A | T | 1 | a0001c0001t0001g0007 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1883+9388A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096569 | ||||||
chr2:231096793
|
G | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+9612G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096793 | ||||||
chr2:231096868
|
G | T | 46 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0119others(43): Show | 48 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1883+9687G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096868 | ||||||
chr2:231096876
|
A | T | 1 | a0001c0001t0001g0315 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1883+9695A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096876 | ||||||
chr2:231097299
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1883+10118T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097299 | ||||||
chr2:231097341
|
T | C | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+10160T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097341 | ||||||
chr2:231097432
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+10251T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097432 | ||||||
chr2:231097451
|
T | C | 1 | a0001c0001t0003g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1883+10270T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097451 | ||||||
chr2:231097574
|
G | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+10393G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097574 | ||||||
chr2:231097651
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1883+10470C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097651 | ||||||
chr2:231097771
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1883+10590G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097771 | ||||||
chr2:231098002
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1883+10821G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098002 | ||||||
chr2:231098025
|
C | G | 4 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+10844C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098025 | ||||||
chr2:231098058
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020 | 3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1883+10877G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098058 | ||||||
chr2:231098078
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1883+10897C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098078 | ||||||
chr2:231098094
|
G | T | 2 | a0001c0001t0001g0348a0001c0001t0001g0350 | 2 | HG01069.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1883+10913G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098094 | ||||||
chr2:231098349
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1883+11168A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098349 | ||||||
chr2:231098361
|
CT | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0350others(1): Show | 4 | HG00280.hp2 HG01069.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1883+11183delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098361 | |||||
chr2:231098402
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1883+11221T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098402 | ||||||
chr2:231098447
|
TTC | T | 6 | a0001c0001t0003g0004a0001c0001t0003g0136a0001c0001t0003g0137others(3): Show | 7 | HG03834.hp2 NA18963.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+11278_1883+11 others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098447 | |||||
chr2:231098457
|
CTCTG | C | 4 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0337others(1): Show | 4 | HG02145.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+11280_1883+11 others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098457 | |||||
chr2:231098461
|
G | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+11280G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098461 | ||||||
chr2:231098512
|
T | A | 1 | a0001c0001t0002g0042 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1883+11331T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098512 | ||||||
chr2:231098543
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+11362T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098543 | ||||||
chr2:231098555
|
TTCTCTC | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0100a0001c0005t0001g0028 | 3 | NA18973.hp1 NA18985.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1883+11391_1883+11 others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098555 | |||||
chr2:231098780
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1883+11599G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098780 | ||||||
chr2:231099061
|
C | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+11880C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099061 | ||||||
chr2:231099075
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1883+11894G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099075 | ||||||
chr2:231099180
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0178a0001c0001t0001g0179others(10): Show | 14 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1883+11999C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099180 | ||||||
chr2:231099181
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+12000G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099181 | ||||||
chr2:231099335
|
T | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+12154T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099335 | ||||||
chr2:231099396
|
G | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+12215G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099396 | ||||||
chr2:231099443
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+12262C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099443 | ||||||
chr2:231099473
|
C | G | 1 | a0001c0001t0001g0325 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1883+12292C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099473 | ||||||
chr2:231099813
|
T | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+12632T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099813 | ||||||
chr2:231099859
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1883+12678C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099859 | ||||||
chr2:231099946
|
C | T | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+12765C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099946 | ||||||
chr2:231100129
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1883+12948G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100129 | ||||||
chr2:231100151
|
C | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0312a0001c0001t0001g0313 | 3 | HG01928.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1883+12970C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100151 | ||||||
chr2:231100171
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+12990T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100171 | ||||||
chr2:231100180
|
T | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+12999T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100180 | ||||||
chr2:231100250
|
T | C | 2 | a0001c0001t0003g0354a0001c0001t0003g0355 | 2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1883+13069T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100250 | ||||||
chr2:231100280
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1883+13099A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100280 | ||||||
chr2:231100351
|
G | A | 58 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(55): Show | 60 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1883+13170G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100351 | ||||||
chr2:231100380
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+13199C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100380 | ||||||
chr2:231100380
|
C | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1883+13199C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100380 | ||||||
chr2:231100491
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+13310G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100491 | ||||||
chr2:231100698
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0342 | 3 | HG01070.hp2 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1883+13517A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100698 | ||||||
chr2:231100891
|
C | G | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1883+13710C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100891 | ||||||
chr2:231101109
|
T | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+13928T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101109 | ||||||
chr2:231101379
|
A | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0353 | 3 | HG03490.hp1 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1883+14198A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101379 | ||||||
chr2:231101442
|
T | C | 6 | a0001c0001t0002g0034a0001c0001t0003g0133a0001c0001t0003g0134others(3): Show | 6 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1883+14261T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101442 | ||||||
chr2:231101569
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+14388T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101569 | ||||||
chr2:231101592
|
A | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+14411A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101592 | ||||||
chr2:231101752
|
C | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+14571C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101752 | ||||||
chr2:231102426
|
A | G | 1 | a0001c0001t0001g0006 | 2 | NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1883+15245A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102426 | ||||||
chr2:231102496
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1883+15315A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102496 | ||||||
chr2:231102524
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1883+15343A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102524 | ||||||
chr2:231102780
|
T | A | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+15599T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102780 | ||||||
chr2:231102873
|
GTTATATT others(16): Show |
G | 6 | a0001c0001t0001g0215a0001c0001t0001g0281a0001c0001t0003g0157others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1883+15715_1883+15 others(29): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231102873 | |||||
chr2:231102896
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 252 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1883+15715A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102896 | ||||||
chr2:231102969
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0003g0154 | 2 | HG02155.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1883+15788C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102969 | ||||||
chr2:231102976
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0193others(81): Show | 86 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.1883+15795T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102976 | ||||||
chr2:231103172
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+15991T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231103172 | ||||||
chr2:231103235
|
C | T | 1 | a0001c0001t0002g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1883+16054C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231103235 | ||||||
chr2:231103518
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+16337G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231103518 | ||||||
chr2:231104057
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1883+16876G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104057 | ||||||
chr2:231104101
|
A | AGTT | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1883+16921_1883+16 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231104101 | |||||
chr2:231104206
|
G | T | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1883+17025G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104206 | ||||||
chr2:231104333
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+17152C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104333 | ||||||
chr2:231104336
|
CT | C | 4 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+17157delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231104336 | |||||
chr2:231104367
|
T | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0002t0004g0023others(5): Show | 8 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1883+17186T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104367 | ||||||
chr2:231104368
|
A | G | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+17187A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104368 | ||||||
chr2:231104405
|
A | G | 2 | a0001c0001t0003g0003a0001c0001t0003g0121 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1883+17224A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104405 | ||||||
chr2:231104438
|
A | G | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+17257A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104438 | ||||||
chr2:231104550
|
C | CT | 82 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0193others(79): Show | 84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.1883+17370dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231104550 | |||||
chr2:231104576
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1883+17395C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104576 | ||||||
chr2:231104612
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1883+17431G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104612 | ||||||
chr2:231104669
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1883+17488C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104669 | ||||||
chr2:231104734
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1883+17553C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104734 | ||||||
chr2:231104754
|
C | T | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+17573C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104754 | ||||||
chr2:231104840
|
A | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1883+17659A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104840 | ||||||
chr2:231104942
|
G | A | 2 | a0001c0001t0002g0068a0001c0001t0002g0345 | 2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1883+17761G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104942 | ||||||
chr2:231104965
|
G | A | 1 | a0001c0001t0002g0345 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1883+17784G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104965 | ||||||
chr2:231105222
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1883+18041T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105222 | ||||||
chr2:231105322
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+18141G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105322 | ||||||
chr2:231105455
|
G | C | 1 | a0001c0001t0003g0141 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1883+18274G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105455 | ||||||
chr2:231105648
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1883+18467G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105648 | ||||||
chr2:231105794
|
CCACTAAC others(5): Show |
C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+18621_1883+18 others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231105794 | |||||
chr2:231105911
|
T | C | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020 | 3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1883+18730T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105911 | ||||||
chr2:231105954
|
A | AT | 47 | a0001c0001t0001g0086a0001c0001t0001g0249a0001c0001t0001g0261others(44): Show | 47 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1883+18783dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231105954 | |||||
chr2:231106018
|
G | GT | 8 | a0001c0001t0001g0021a0001c0001t0002g0052a0001c0001t0002g0081others(5): Show | 8 | HG01981.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1883+18852dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231106018 | |||||
chr2:231106018
|
GT | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1883+18852delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231106018 | |||||
chr2:231106024
|
T | G | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0265others(1): Show | 4 | HG03688.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+18843T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231106024 | ||||||
chr2:231106207
|
T | A | 1 | a0001c0001t0001g0312 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1883+19026T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231106207 | ||||||
chr2:231106960
|
C | A | 1 | a0001c0001t0003g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1883+19779C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231106960 | ||||||
chr2:231107089
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1883+19908G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107089 | ||||||
chr2:231107144
|
A | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+19963A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107144 | ||||||
chr2:231107208
|
A | C | 1 | a0001c0001t0002g0109 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1883+20027A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107208 | ||||||
chr2:231107461
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0193others(78): Show | 83 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.1883+20280A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107461 | ||||||
chr2:231107683
|
G | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+20502G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107683 | ||||||
chr2:231107829
|
C | T | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG01243.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1883+20648C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107829 | ||||||
chr2:231107870
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1883+20689T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107870 | ||||||
chr2:231108649
|
G | A | 6 | a0001c0001t0001g0022a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1883+21468G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108649 | ||||||
chr2:231108688
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1883+21507A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108688 | ||||||
chr2:231108702
|
T | C | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+21521T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108702 | ||||||
chr2:231108711
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+21530G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108711 | ||||||
chr2:231108732
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1883+21551G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108732 | ||||||
chr2:231108991
|
C | G | 1 | a0001c0001t0002g0107 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1883+21810C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108991 | ||||||
chr2:231109120
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1883+21939C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109120 | ||||||
chr2:231109341
|
C | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02258.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1883+22160C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109341 | ||||||
chr2:231109535
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0244others(4): Show | 9 | NA18951.hp1 NA18955.hp1 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1883+22354A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109535 | ||||||
chr2:231109548
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1883+22367C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109548 | ||||||
chr2:231109654
|
A | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+22473A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109654 | ||||||
chr2:231110209
|
A | G | 1 | a0001c0001t0003g0141 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1883+23028A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110209 | ||||||
chr2:231110755
|
A | G | 1 | a0001c0001t0003g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1883+23574A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110755 | ||||||
chr2:231110831
|
A | G | 5 | a0001c0001t0002g0040a0001c0001t0002g0094a0001c0001t0002g0100others(2): Show | 5 | NA18957.hp2 NA18967.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+23650A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110831 | ||||||
chr2:231110832
|
C | G | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | NA18952.hp1 NA18957.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1883+23651C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110832 | ||||||
chr2:231110868
|
T | C | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+23687T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110868 | ||||||
chr2:231111329
|
A | C | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1883+24148A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111329 | ||||||
chr2:231111746
|
T | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1883+24565T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111746 | ||||||
chr2:231111865
|
G | A | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+24684G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111865 | ||||||
chr2:231111901
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+24720A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111901 | ||||||
chr2:231111947
|
G | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+24766G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111947 | ||||||
chr2:231112117
|
C | T | 2 | a0001c0001t0003g0164a0001c0001t0003g0167 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1883+24936C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112117 | ||||||
chr2:231112227
|
A | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | NA18979.hp2 NA18988.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1883+25046A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112227 | ||||||
chr2:231112254
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1883+25073C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112254 | ||||||
chr2:231112288
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1883+25107C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112288 | ||||||
chr2:231112382
|
T | C | 1 | a0001c0001t0003g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1883+25201T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112382 | ||||||
chr2:231112516
|
C | T | 3 | a0001c0002t0004g0024a0001c0002t0004g0025a0001c0002t0004g0026 | 3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+25335C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112516 | ||||||
chr2:231112600
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1883+25419A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112600 | ||||||
chr2:231112723
|
G | A | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+25542G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112723 | ||||||
chr2:231112725
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1883+25544A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112725 | ||||||
chr2:231112779
|
A | T | 1 | a0001c0001t0003g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1883+25598A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112779 | ||||||
chr2:231112813
|
C | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1883+25632C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112813 | ||||||
chr2:231112816
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1883+25635A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112816 | ||||||
chr2:231112821
|
CT | C | 7 | a0001c0001t0001g0021a0001c0002t0004g0023a0001c0002t0004g0024others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+25641delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112821 | ||||||
chr2:231112914
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1883+25733C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112914 | ||||||
chr2:231112992
|
C | T | 1 | a0001c0001t0001g0319 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1884-25744C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112992 | ||||||
chr2:231113089
|
G | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0167 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1884-25647G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113089 | ||||||
chr2:231113149
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1884-25587G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113149 | ||||||
chr2:231113262
|
A | G | 2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1884-25474A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113262 | ||||||
chr2:231113285
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-25451C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113285 | ||||||
chr2:231113495
|
T | C | 1 | a0001c0001t0002g0352 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1884-25241T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113495 | ||||||
chr2:231113961
|
A | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-24775A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113961 | ||||||
chr2:231114359
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0005t0001g0028 | 3 | NA20129.hp2 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1884-24377G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114359 | ||||||
chr2:231114531
|
G | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | HG01069.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1884-24205G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114531 | ||||||
chr2:231114544
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-24192A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114544 | ||||||
chr2:231114567
|
T | C | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-24169T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114567 | ||||||
chr2:231114641
|
C | T | 41 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(38): Show | 43 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1884-24095C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114641 | ||||||
chr2:231114806
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1884-23930T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114806 | ||||||
chr2:231114834
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1884-23902A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114834 | ||||||
chr2:231115150
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1884-23586T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115150 | ||||||
chr2:231115162
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1884-23574G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115162 | ||||||
chr2:231115280
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-23456C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115280 | ||||||
chr2:231115305
|
C | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 264 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1884-23431C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115305 | ||||||
chr2:231115493
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1884-23243G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115493 | ||||||
chr2:231115716
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-23020A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115716 | ||||||
chr2:231115720
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1884-23016G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115720 | ||||||
chr2:231115860
|
C | G | 1 | a0001c0001t0001g0249 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1884-22876C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115860 | ||||||
chr2:231116063
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 208 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1884-22673A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116063 | ||||||
chr2:231116154
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1884-22582A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116154 | ||||||
chr2:231116326
|
C | G | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1884-22410C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116326 | ||||||
chr2:231116390
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-22346A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116390 | ||||||
chr2:231116393
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-22343T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116393 | ||||||
chr2:231116429
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1884-22307G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116429 | ||||||
chr2:231116433
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1884-22303C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116433 | ||||||
chr2:231116507
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1884-22229G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116507 | ||||||
chr2:231116605
|
A | G | 1 | a0002c0003t0002g0079 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1884-22131A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116605 | ||||||
chr2:231116645
|
G | GT | 17 | a0001c0001t0001g0022a0001c0001t0003g0117a0001c0001t0003g0118others(14): Show | 17 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1884-22085dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231116645 | |||||
chr2:231116662
|
T | A | 1 | a0001c0002t0004g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884-22074T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116662 | ||||||
chr2:231116747
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-21989A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116747 | ||||||
chr2:231116790
|
A | T | 1 | a0001c0001t0001g0224 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1884-21946A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116790 | ||||||
chr2:231117062
|
A | G | 7 | a0001c0001t0002g0010a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | NA18966.hp1 NA19003.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-21674A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117062 | ||||||
chr2:231117119
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1884-21617A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117119 | ||||||
chr2:231117182
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1884-21554G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117182 | ||||||
chr2:231117196
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-21540T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117196 | ||||||
chr2:231117249
|
A | G | 1 | a0001c0001t0003g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1884-21487A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117249 | ||||||
chr2:231117278
|
A | G | 339 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(336): Show | 348 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.1884-21458A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117278 | ||||||
chr2:231117669
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1884-21067T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117669 | ||||||
chr2:231117791
|
C | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1884-20945C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117791 | ||||||
chr2:231118033
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02258.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1884-20703T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118033 | ||||||
chr2:231118112
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(230): Show | 241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1884-20624G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118112 | ||||||
chr2:231118124
|
T | TAATAGTA others(278): Show |
7 | a0001c0001t0003g0118a0001c0001t0003g0122a0001c0001t0003g0123others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-20597_1884-20 others(291): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118124 | |||||
chr2:231118124
|
T | TAATAGTA others(279): Show |
3 | a0001c0001t0003g0117a0001c0001t0003g0124a0001c0001t0003g0128 | 3 | HG02055.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1884-20597_1884-20 others(292): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118124 | |||||
chr2:231118236
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-20500T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118236 | ||||||
chr2:231118257
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | NA18940.hp1 NA18973.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-20479A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118257 | ||||||
chr2:231118295
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-20441C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118295 | ||||||
chr2:231118437
|
G | GT | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-20297dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118437 | |||||
chr2:231118461
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-20275G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118461 | ||||||
chr2:231118525
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0339 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1884-20211G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118525 | ||||||
chr2:231118668
|
T | G | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(29): Show | 34 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1884-20068T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118668 | ||||||
chr2:231118729
|
A | G | 1 | a0001c0001t0003g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1884-20007A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118729 | ||||||
chr2:231118978
|
AAAAG | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(68): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1884-19752_1884-19 others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118978 | |||||
chr2:231119110
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1884-19626A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119110 | ||||||
chr2:231119436
|
T | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-19300T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119436 | ||||||
chr2:231119439
|
C | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-19297C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119439 | ||||||
chr2:231119504
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1884-19232C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119504 | ||||||
chr2:231119514
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0266 | 2 | HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1884-19222A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119514 | ||||||
chr2:231119651
|
A | G | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0265others(1): Show | 4 | HG03688.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-19085A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119651 | ||||||
chr2:231119869
|
C | CA | 27 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0019others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1884-18845dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | |||||
chr2:231119869
|
CA | C | 37 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0188others(34): Show | 37 | HG00673.hp2 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.1884-18845delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | |||||
chr2:231119869
|
CAA | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 213 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1884-18846_1884-18 others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | |||||
chr2:231119869
|
CAAA | C | 7 | a0001c0001t0001g0311a0001c0001t0003g0158a0001c0002t0004g0023others(4): Show | 7 | HG01169.hp1 HG02083.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-18847_1884-18 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | |||||
chr2:231119950
|
C | CT | 7 | a0001c0001t0001g0177a0001c0001t0001g0264a0001c0001t0001g0302others(4): Show | 7 | HG00735.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-18770dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119950 | |||||
chr2:231119950
|
CT | C | 6 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0065others(3): Show | 6 | HG00438.hp2 HG00609.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1884-18770delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119950 | |||||
chr2:231119966
|
T | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-18770T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119966 | ||||||
chr2:231119984
|
AC | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-18748delC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119984 | |||||
chr2:231120241
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1884-18495C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120241 | ||||||
chr2:231120242
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-18494G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120242 | ||||||
chr2:231120457
|
AC | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0342 | 3 | HG01070.hp2 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1884-18278delC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120457 | ||||||
chr2:231120542
|
A | G | 1 | a0001c0001t0002g0038 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1884-18194A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120542 | ||||||
chr2:231120543
|
A | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-18193A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120543 | ||||||
chr2:231120562
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1884-18174A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120562 | ||||||
chr2:231120822
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0266 | 3 | HG01928.hp1 HG02300.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1884-17914C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120822 | ||||||
chr2:231120827
|
G | A | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884-17909G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120827 | ||||||
chr2:231121396
|
TAATAAAC others(6): Show |
T | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0093 | 3 | NA18988.hp2 NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1884-17337_1884-17 others(19): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231121396 | |||||
chr2:231121740
|
A | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-16996A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121740 | ||||||
chr2:231121979
|
A | G | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16757A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121979 | ||||||
chr2:231121980
|
T | C | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16756T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121980 | ||||||
chr2:231121981
|
C | CTGTACAG | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16755_1884-16 others(13): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121981 | ||||||
chr2:231121982
|
A | T | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16754A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121982 | ||||||
chr2:231121984
|
A | C | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16752A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121984 | ||||||
chr2:231122018
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-16718T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231122018 | ||||||
chr2:231122442
|
A | C | 1 | a0001c0001t0003g0141 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1884-16294A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231122442 | ||||||
chr2:231122494
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-16242A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231122494 | ||||||
chr2:231122766
|
AGGAACAC others(4): Show |
A | 1 | a0001c0001t0001g0249 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1884-15968_1884-15 others(17): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231122766 | |||||
chr2:231123014
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1884-15722G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123014 | ||||||
chr2:231123037
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0178a0001c0001t0001g0180others(7): Show | 11 | HG00544.hp2 HG00673.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1884-15699C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123037 | ||||||
chr2:231123122
|
A | G | 1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1884-15614A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123122 | ||||||
chr2:231123176
|
T | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-15560T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123176 | ||||||
chr2:231123241
|
C | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1884-15495C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123241 | ||||||
chr2:231123386
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-15350A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123386 | ||||||
chr2:231123388
|
G | T | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1884-15348G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123388 | ||||||
chr2:231123613
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-15123C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123613 | ||||||
chr2:231123638
|
T | C | 1 | a0001c0001t0006g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1884-15098T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123638 | ||||||
chr2:231123674
|
A | G | 7 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-15062A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123674 | ||||||
chr2:231123910
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0277 | 2 | NA18943.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1884-14826C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123910 | ||||||
chr2:231123912
|
A | G | 2 | a0001c0001t0003g0003a0001c0001t0003g0121 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1884-14824A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123912 | ||||||
chr2:231124099
|
C | T | 2 | a0001c0001t0002g0068a0001c0001t0002g0345 | 2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1884-14637C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124099 | ||||||
chr2:231124141
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0193others(77): Show | 82 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.1884-14595A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124141 | ||||||
chr2:231124347
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1884-14389C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124347 | ||||||
chr2:231124933
|
C | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1884-13803C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124933 | ||||||
chr2:231125321
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1884-13415T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125321 | ||||||
chr2:231125386
|
A | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0193others(79): Show | 84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.1884-13350A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125386 | ||||||
chr2:231125657
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 207 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1884-13079A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125657 | ||||||
chr2:231125734
|
A | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0261 | 3 | NA18952.hp2 NA19077.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1884-13002A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125734 | ||||||
chr2:231125761
|
A | C | 1 | a0001c0001t0002g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1884-12975A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125761 | ||||||
chr2:231125953
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1884-12783G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125953 | ||||||
chr2:231126135
|
G | T | 2 | a0001c0001t0003g0131a0001c0001t0003g0132 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1884-12601G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126135 | ||||||
chr2:231126152
|
C | T | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1884-12584C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126152 | ||||||
chr2:231126244
|
C | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0093 | 3 | NA18988.hp2 NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1884-12492C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126244 | ||||||
chr2:231126304
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1884-12432G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126304 | ||||||
chr2:231126609
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1884-12127A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126609 | ||||||
chr2:231126638
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1884-12098A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126638 | ||||||
chr2:231126808
|
G | A | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884-11928G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126808 | ||||||
chr2:231126850
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1884-11886T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126850 | ||||||
chr2:231126903
|
T | A | 7 | a0001c0001t0003g0141a0001c0001t0003g0149a0001c0001t0003g0150others(4): Show | 7 | NA18972.hp1 NA18975.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884-11833T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126903 | ||||||
chr2:231127028
|
C | T | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884-11708C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127028 | ||||||
chr2:231127052
|
C | T | 1 | a0001c0001t0003g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1884-11684C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127052 | ||||||
chr2:231127274
|
C | A | 3 | a0001c0001t0002g0064a0001c0001t0002g0345a0001c0002t0004g0026 | 3 | HG03139.hp1 NA18983.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1884-11462C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127274 | ||||||
chr2:231127274
|
C | CA | 11 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0199others(8): Show | 11 | HG00438.hp2 HG01070.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1884-11448dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231127274 | |||||
chr2:231127277
|
A | C | 2 | a0001c0001t0001g0008a0001c0001t0003g0119 | 3 | NA18522.hp2 NA19002.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1884-11459A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127277 | ||||||
chr2:231127288
|
AC | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0141others(1): Show | 4 | NA18951.hp2 NA18972.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1884-11447delC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127288 | ||||||
chr2:231127289
|
C | A | 30 | a0001c0001t0003g0004a0001c0001t0003g0133a0001c0001t0003g0134others(27): Show | 31 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1884-11447C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127289 | ||||||
chr2:231127499
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1884-11237C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127499 | ||||||
chr2:231127500
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1884-11236G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127500 | ||||||
chr2:231127543
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-11193C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127543 | ||||||
chr2:231127597
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1884-11139G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127597 | ||||||
chr2:231127600
|
T | C | 2 | a0001c0001t0003g0133a0001c0001t0003g0134 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1884-11136T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127600 | ||||||
chr2:231127630
|
G | A | 1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1884-11106G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127630 | ||||||
chr2:231128054
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1884-10682A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128054 | ||||||
chr2:231128092
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0328 | 2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1884-10644G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128092 | ||||||
chr2:231128092
|
G | C | 1 | a0001c0001t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1884-10644G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128092 | ||||||
chr2:231128231
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-10505T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128231 | ||||||
chr2:231128234
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1884-10502T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128234 | ||||||
chr2:231128264
|
A | G | 1 | a0002c0003t0002g0079 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1884-10472A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128264 | ||||||
chr2:231128324
|
A | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1884-10412A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128324 | ||||||
chr2:231128352
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-10384C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128352 | ||||||
chr2:231128473
|
A | G | 1 | a0001c0001t0001g0323 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1884-10263A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128473 | ||||||
chr2:231128484
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-10252G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128484 | ||||||
chr2:231128525
|
C | T | 6 | a0001c0001t0003g0355a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1884-10211C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128525 | ||||||
chr2:231128598
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1884-10138A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128598 | ||||||
chr2:231129024
|
G | T | 36 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(33): Show | 38 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1884-9712G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129024 | ||||||
chr2:231129048
|
T | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-9688T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129048 | ||||||
chr2:231129332
|
T | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-9404T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129332 | ||||||
chr2:231129479
|
A | G | 2 | a0001c0001t0003g0136a0001c0001t0003g0138 | 2 | NA18963.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1884-9257A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129479 | ||||||
chr2:231129666
|
A | G | 1 | a0001c0001t0002g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1884-9070A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129666 | ||||||
chr2:231129747
|
A | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0221a0001c0001t0001g0226 | 3 | NA18947.hp2 NA18950.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1884-8989A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129747 | ||||||
chr2:231129879
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1884-8857A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129879 | ||||||
chr2:231130088
|
G | A | 2 | a0001c0001t0003g0141a0001c0001t0003g0160 | 2 | NA18972.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1884-8648G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231130088 | ||||||
chr2:231130580
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1884-8156C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231130580 | ||||||
chr2:231130887
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1884-7849G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231130887 | ||||||
chr2:231131018
|
G | T | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1884-7718G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131018 | ||||||
chr2:231131056
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1884-7680G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131056 | ||||||
chr2:231131462
|
TAGAAAGT others(317): Show |
T | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1884-7254_1884-693 others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231131462 | |||||
chr2:231131761
|
C | CA | 19 | a0001c0001t0001g0086a0001c0001t0002g0014a0001c0001t0002g0015others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1884-6949dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231131761 | |||||
chr2:231131761
|
CA | C | 9 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0070others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1884-6949delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231131761 | |||||
chr2:231131851
|
A | G | 1 | a0001c0006t0002g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1884-6885A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131851 | ||||||
chr2:231131862
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.1884-6874G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131862 | ||||||
chr2:231132076
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1884-6660T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132076 | ||||||
chr2:231132095
|
C | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(68): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1884-6641C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132095 | ||||||
chr2:231132241
|
A | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1884-6495A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132241 | ||||||
chr2:231132618
|
G | GC | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0265others(1): Show | 4 | HG03688.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-6117dupC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231132618 | |||||
chr2:231132624
|
A | G | 18 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(15): Show | 18 | HG01243.hp1 HG02055.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1884-6112A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132624 | ||||||
chr2:231132896
|
C | A | 1 | a0001c0001t0001g0255 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1884-5840C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132896 | ||||||
chr2:231133106
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1884-5630A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133106 | ||||||
chr2:231133234
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-5502G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133234 | ||||||
chr2:231133245
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-5491C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133245 | ||||||
chr2:231133273
|
C | T | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-5463C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133273 | ||||||
chr2:231133296
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-5440G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133296 | ||||||
chr2:231133383
|
C | T | 1 | a0001c0001t0003g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1884-5353C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133383 | ||||||
chr2:231133416
|
G | A | 5 | a0001c0001t0001g0022a0001c0002t0004g0023a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03139.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-5320G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133416 | ||||||
chr2:231133581
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1884-5155C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133581 | ||||||
chr2:231134139
|
A | G | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1884-4597A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231134139 | ||||||
chr2:231134322
|
G | A | 3 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0001t0003g0159 | 3 | HG01168.hp1 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1884-4414G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231134322 | ||||||
chr2:231134733
|
G | A | 2 | a0001c0001t0002g0095a0001c0001t0002g0105 | 2 | HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1884-4003G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231134733 | ||||||
chr2:231135057
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1884-3679A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135057 | ||||||
chr2:231135110
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1884-3626T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135110 | ||||||
chr2:231135113
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-3623A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135113 | ||||||
chr2:231135164
|
G | C | 8 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1884-3572G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135164 | ||||||
chr2:231135175
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1884-3561G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135175 | ||||||
chr2:231135186
|
G | T | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1884-3550G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135186 | ||||||
chr2:231135350
|
G | A | 4 | a0001c0001t0001g0303a0001c0001t0001g0316a0001c0001t0001g0317others(1): Show | 4 | NA18943.hp1 NA18975.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1884-3386G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135350 | ||||||
chr2:231135443
|
G | A | 6 | a0001c0001t0002g0083a0001c0001t0002g0087a0001c0001t0002g0091others(3): Show | 6 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1884-3293G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135443 | ||||||
chr2:231135701
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225 | 3 | HG03490.hp2 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1884-3035A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135701 | ||||||
chr2:231135831
|
A | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-2905A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135831 | ||||||
chr2:231135999
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0176 | 3 | NA18940.hp1 NA18973.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1884-2737G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135999 | ||||||
chr2:231136219
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1884-2517C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136219 | ||||||
chr2:231136227
|
T | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-2509T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136227 | ||||||
chr2:231136535
|
A | G | 1 | a0001c0001t0003g0136 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1884-2201A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136535 | ||||||
chr2:231136807
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-1929A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136807 | ||||||
chr2:231136969
|
ATT | A | 7 | a0001c0001t0003g0141a0001c0001t0003g0149a0001c0001t0003g0150others(4): Show | 7 | NA18972.hp1 NA18975.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884-1766_1884-176 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136969 | ||||||
chr2:231137057
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1884-1679A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137057 | ||||||
chr2:231137148
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1884-1588C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137148 | ||||||
chr2:231137211
|
G | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1884-1525G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137211 | ||||||
chr2:231137412
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1884-1324C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137412 | ||||||
chr2:231137424
|
A | T | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-1312A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137424 | ||||||
chr2:231137487
|
A | G | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884-1249A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137487 | ||||||
chr2:231137556
|
T | A | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1884-1180T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137556 | ||||||
chr2:231137721
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-1015A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137721 | ||||||
chr2:231138345
|
G | A | 2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1884-391G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138345 | ||||||
chr2:231138389
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-347T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138389 | ||||||
chr2:231138475
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-261C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138475 | ||||||
chr2:231138675
|
T | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-61T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138675 | ||||||
chr2:231138703
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1884-33A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138703 | ||||||
chr2:231139004
|
C | T | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1998+154C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139004 | ||||||
chr2:231139038
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1998+188A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139038 | ||||||
chr2:231139051
|
A | G | 1 | a0001c0001t0002g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1998+201A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139051 | ||||||
chr2:231139118
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1998+268G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139118 | ||||||
chr2:231139123
|
T | C | 2 | a0001c0001t0003g0003a0001c0001t0003g0121 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1998+273T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139123 | ||||||
chr2:231139124
|
G | GT | 7 | a0001c0001t0001g0021a0001c0001t0001g0237a0001c0001t0001g0250others(4): Show | 7 | HG01952.hp1 HG03225.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.1998+282dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139124 | |||||
chr2:231139166
|
CTT | C | 4 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998+318_1998+319d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139166 | |||||
chr2:231139250
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1998+400C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139250 | ||||||
chr2:231139291
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1998+441A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139291 | ||||||
chr2:231139314
|
C | CT | 8 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0002g0058others(5): Show | 8 | HG01074.hp1 HG01123.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1998+487dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | |||||
chr2:231139314
|
CT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 184 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1998+487delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | |||||
chr2:231139314
|
CTT | C | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(51): Show | 56 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1998+486_1998+487d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | |||||
chr2:231139314
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1998+477_1998+487d others(13): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | |||||
chr2:231139320
|
T | C | 9 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(6): Show | 9 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1998+470T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139320 | ||||||
chr2:231139558
|
T | TA | 178 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 184 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1998+725dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139558 | |||||
chr2:231139558
|
T | TAA | 44 | a0001c0001t0001g0086a0001c0001t0001g0178a0001c0001t0001g0232others(41): Show | 46 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1998+724_1998+725d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139558 | |||||
chr2:231139573
|
A | AG | 3 | a0001c0002t0004g0024a0001c0002t0004g0025a0001c0002t0004g0026 | 3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1998+723_1998+724i others(3): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139573 | ||||||
chr2:231139576
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1998+726G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139576 | ||||||
chr2:231139579
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0003g0128 | 2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1998+729G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139579 | ||||||
chr2:231139755
|
G | A | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1998+905G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139755 | ||||||
chr2:231139829
|
T | C | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1998+979T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139829 | ||||||
chr2:231140220
|
G | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1998+1370G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140220 | ||||||
chr2:231140357
|
A | G | 1 | a0001c0002t0004g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1998+1507A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140357 | ||||||
chr2:231140390
|
G | C | 4 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1998+1540G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140390 | ||||||
chr2:231140406
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1998+1556G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140406 | ||||||
chr2:231140495
|
C | CA | 17 | a0001c0001t0001g0130a0001c0001t0001g0184a0001c0001t0001g0195others(14): Show | 17 | HG01928.hp1 HG01981.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1998+1665dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231140495 | |||||
chr2:231140495
|
CA | C | 12 | a0001c0001t0001g0176a0001c0001t0001g0199a0001c0001t0001g0236others(9): Show | 12 | HG01070.hp2 HG01516.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1998+1665delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231140495 | |||||
chr2:231140786
|
G | C | 1 | a0001c0001t0002g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1998+1936G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140786 | ||||||
chr2:231141035
|
C | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045 | 3 | HG02027.hp1 NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1998+2185C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141035 | ||||||
chr2:231141305
|
G | GA | 9 | a0001c0001t0001g0199a0001c0001t0001g0268a0001c0001t0001g0291others(6): Show | 9 | HG01981.hp1 HG02015.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1998+2469dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141305 | |||||
chr2:231141305
|
GA | G | 6 | a0001c0001t0001g0022a0001c0001t0002g0055a0001c0001t0002g0072others(3): Show | 6 | HG01168.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1998+2469delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141305 | |||||
chr2:231141395
|
C | T | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(56): Show | 61 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1998+2545C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141395 | ||||||
chr2:231141412
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1998+2562C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141412 | ||||||
chr2:231141420
|
ACT | A | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0266others(1): Show | 4 | HG01928.hp1 HG02300.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998+2571_1998+257 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141420 | ||||||
chr2:231141420
|
ACTT | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(72): Show | 77 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1998+2571_1998+257 others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141420 | ||||||
chr2:231141421
|
C | CT | 15 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0213others(12): Show | 15 | HG02280.hp1 HG02738.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.1998+2590dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141421 | |||||
chr2:231141421
|
CT | C | 12 | a0001c0001t0002g0073a0001c0001t0002g0087a0001c0001t0003g0117others(9): Show | 12 | HG01168.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1998+2590delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141421 | |||||
chr2:231141496
|
G | C | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1998+2646G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141496 | ||||||
chr2:231141568
|
C | T | 4 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1998+2718C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141568 | ||||||
chr2:231141583
|
AT | A | 7 | a0001c0001t0002g0011a0001c0001t0002g0102a0001c0002t0004g0023others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1998+2748delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141583 | |||||
chr2:231141737
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1998+2887G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141737 | ||||||
chr2:231142043
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1998+3193C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142043 | ||||||
chr2:231142044
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1998+3194G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142044 | ||||||
chr2:231142072
|
G | A | 48 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1998+3222G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142072 | ||||||
chr2:231142208
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1998+3358C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142208 | ||||||
chr2:231142510
|
C | T | 1 | a0001c0001t0002g0044 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1998+3660C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142510 | ||||||
chr2:231142541
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998+3691G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142541 | ||||||
chr2:231142568
|
C | A | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1999-3672C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142568 | ||||||
chr2:231142636
|
T | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(33): Show | 38 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1999-3604T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142636 | ||||||
chr2:231142713
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1999-3527C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142713 | ||||||
chr2:231142865
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1999-3375T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142865 | ||||||
chr2:231143065
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(79): Show | 84 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1999-3175T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143065 | ||||||
chr2:231143140
|
A | AT | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1999-3090dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143140 | |||||
chr2:231143140
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1999-3100A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143140 | ||||||
chr2:231143187
|
G | GGGTTT | 5 | a0001c0001t0001g0175a0001c0001t0001g0187a0001c0001t0001g0193others(2): Show | 5 | HG02886.hp1 HG03579.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999-2997_1999-299 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | |||||
chr2:231143187
|
GGGTTT | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0086others(134): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1999-2997_1999-299 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | |||||
chr2:231143187
|
GGGTTTGG others(3): Show |
G | 41 | a0001c0001t0001g0022a0001c0001t0001g0248a0001c0001t0001g0249others(38): Show | 43 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.1999-3002_1999-299 others(14): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | |||||
chr2:231143187
|
GGGTTTGG others(8): Show |
G | 116 | a0001c0001t0001g0008a0001c0001t0001g0200a0001c0001t0001g0206others(113): Show | 118 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1999-3007_1999-299 others(19): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | |||||
chr2:231143187
|
GGGTTTGG others(13): Show |
G | 8 | a0001c0001t0002g0035a0001c0001t0002g0067a0001c0001t0002g0096others(5): Show | 8 | HG00733.hp1 HG03017.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1999-3012_1999-299 others(24): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | |||||
chr2:231143244
|
G | C | 2 | a0001c0001t0002g0068a0001c0001t0002g0345 | 2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1999-2996G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143244 | ||||||
chr2:231143337
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-2903C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143337 | ||||||
chr2:231143339
|
C | G | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1999-2901C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143339 | ||||||
chr2:231143441
|
G | A | 4 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999-2799G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143441 | ||||||
chr2:231143591
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1999-2649C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143591 | ||||||
chr2:231143620
|
T | C | 1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1999-2620T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143620 | ||||||
chr2:231143674
|
G | C | 1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1999-2566G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143674 | ||||||
chr2:231143725
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1999-2515A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143725 | ||||||
chr2:231143759
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1999-2481A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143759 | ||||||
chr2:231143836
|
A | G | 3 | a0001c0001t0002g0029a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG03927.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1999-2404A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143836 | ||||||
chr2:231143945
|
T | C | 1 | a0001c0006t0002g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1999-2295T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143945 | ||||||
chr2:231144130
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-2110G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144130 | ||||||
chr2:231144159
|
G | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1999-2081G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144159 | ||||||
chr2:231144211
|
C | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(88): Show | 93 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1999-2029C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144211 | ||||||
chr2:231144252
|
C | CT | 6 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0047others(3): Show | 6 | NA18968.hp1 NA18972.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-1973dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144252 | |||||
chr2:231144333
|
C | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(62): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1999-1907C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144333 | ||||||
chr2:231144336
|
C | T | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1999-1904C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144336 | ||||||
chr2:231144356
|
A | T | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1999-1884A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144356 | ||||||
chr2:231144401
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1999-1839G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144401 | ||||||
chr2:231144418
|
A | AT | 29 | a0001c0001t0001g0021a0001c0001t0002g0010a0001c0001t0002g0011others(26): Show | 29 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1999-1790dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
AT | A | 6 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0054others(3): Show | 6 | HG00323.hp1 HG01169.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-1790delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
ATTT | A | 26 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0001t0001g0210others(23): Show | 26 | HG00438.hp1 HG00544.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1999-1792_1999-179 others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
ATTTT | A | 87 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 90 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1999-1793_1999-179 others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
ATTTTT | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0086others(115): Show | 122 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999-1794_1999-179 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
ATTTTTT | A | 12 | a0001c0001t0001g0206a0001c0001t0001g0228a0001c0001t0001g0249others(9): Show | 12 | HG01070.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1999-1795_1999-179 others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1999-1800_1999-179 others(15): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1999-1801_1999-179 others(16): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144418
|
ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038 | 3 | HG01074.hp1 HG04204.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1999-1802_1999-179 others(17): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | |||||
chr2:231144423
|
T | A | 1 | a0001c0001t0002g0066 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1999-1817T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144423 | ||||||
chr2:231144498
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1999-1742C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144498 | ||||||
chr2:231144648
|
A | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1999-1592A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144648 | ||||||
chr2:231144662
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA19065.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1999-1578C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144662 | ||||||
chr2:231144757
|
G | T | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1999-1483G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144757 | ||||||
chr2:231144812
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1999-1428A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144812 | ||||||
chr2:231145220
|
T | C | 1 | a0001c0001t0002g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1999-1020T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145220 | ||||||
chr2:231145463
|
A | G | 1 | a0001c0001t0005g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1999-777A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145463 | ||||||
chr2:231145660
|
G | A | 2 | a0001c0001t0002g0040a0001c0001t0002g0100 | 2 | NA18973.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1999-580G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145660 | ||||||
chr2:231145681
|
G | C | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1999-559G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145681 | ||||||
chr2:231145749
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-491C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145749 | ||||||
chr2:231145756
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1999-484G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145756 | ||||||
chr2:231145869
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1999-371G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145869 | ||||||
chr2:231145894
|
C | CA | 46 | a0001c0001t0001g0168a0001c0001t0001g0211a0001c0001t0001g0225others(43): Show | 46 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1999-318dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | |||||
chr2:231145894
|
C | CAA | 14 | a0001c0001t0001g0281a0001c0001t0001g0299a0001c0001t0002g0076others(11): Show | 14 | HG01361.hp1 HG01943.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1999-319_1999-318d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | |||||
chr2:231145894
|
CA | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(102): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1999-318delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | |||||
chr2:231145894
|
CAA | C | 9 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0261others(6): Show | 9 | HG01168.hp1 HG01891.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-319_1999-318d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | |||||
chr2:231145894
|
CAAAAAAA others(2): Show |
C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1999-326_1999-318d others(11): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | |||||
chr2:231145894
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1999-328_1999-318d others(13): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | |||||
chr2:231145966
|
G | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(77): Show | 82 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1999-274G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145966 | ||||||
chr2:231146404
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2115+48C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146404 | ||||||
chr2:231146463
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2115+107A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146463 | ||||||
chr2:231146547
|
T | TAC | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2115+192_2115+193i others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231146547 | |||||
chr2:231146726
|
C | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.2115+370C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146726 | ||||||
chr2:231146842
|
G | T | 1 | a0001c0001t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2115+486G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146842 | ||||||
chr2:231147103
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2115+747C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147103 | ||||||
chr2:231147124
|
C | G | 1 | a0001c0001t0003g0138 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2115+768C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147124 | ||||||
chr2:231147252
|
G | A | 3 | a0001c0001t0001g0294a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG00423.hp1 HG00673.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2115+896G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147252 | ||||||
chr2:231147313
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2115+957G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147313 | ||||||
chr2:231147661
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(76): Show | 81 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.2115+1305T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147661 | ||||||
chr2:231147670
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2115+1314G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147670 | ||||||
chr2:231147675
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2115+1319G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147675 | ||||||
chr2:231147741
|
T | G | 1 | a0001c0001t0002g0031 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2115+1385T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147741 | ||||||
chr2:231148273
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2115+1917A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148273 | ||||||
chr2:231148590
|
G | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.2115+2234G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148590 | ||||||
chr2:231148592
|
A | C | 1 | a0001c0001t0002g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2115+2236A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148592 | ||||||
chr2:231148636
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0176a0001c0001t0001g0177 | 4 | NA18940.hp1 NA18973.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2115+2280A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148636 | ||||||
chr2:231148935
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2115+2579A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148935 | ||||||
chr2:231149073
|
G | A | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2115+2717G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149073 | ||||||
chr2:231149339
|
A | C | 1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2115+2983A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149339 | ||||||
chr2:231149425
|
G | A | 1 | a0001c0001t0003g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2115+3069G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149425 | ||||||
chr2:231149480
|
CA | C | 6 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | NA18942.hp1 NA18980.hp2 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.2115+3131delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231149480 | |||||
chr2:231149482
|
A | G | 14 | a0001c0001t0001g0203a0001c0001t0001g0234a0001c0001t0001g0235others(11): Show | 15 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.2115+3126A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149482 | ||||||
chr2:231149608
|
C | T | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2115+3252C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149608 | ||||||
chr2:231149717
|
C | T | 4 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0337others(1): Show | 4 | HG02145.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2115+3361C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149717 | ||||||
chr2:231149726
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2115+3370A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149726 | ||||||
chr2:231150084
|
G | A | 7 | a0001c0001t0001g0168a0001c0001t0001g0232a0001c0001t0001g0291others(4): Show | 7 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2116-3480G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150084 | ||||||
chr2:231150129
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2116-3435C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150129 | ||||||
chr2:231150189
|
C | CA | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-3367dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231150189 | |||||
chr2:231150260
|
T | C | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | NA18979.hp2 NA18988.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2116-3304T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150260 | ||||||
chr2:231150344
|
CAAG | C | 4 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2116-3219_2116-321 others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150344 | ||||||
chr2:231150423
|
T | G | 6 | a0001c0001t0002g0088a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2116-3141T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150423 | ||||||
chr2:231150659
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2116-2905A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150659 | ||||||
chr2:231150703
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2116-2861C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150703 | ||||||
chr2:231150892
|
C | T | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2116-2672C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150892 | ||||||
chr2:231150920
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2116-2644C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150920 | ||||||
chr2:231151009
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | NA18966.hp1 NA19063.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-2555G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151009 | ||||||
chr2:231151545
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2116-2019T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151545 | ||||||
chr2:231151585
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2116-1979C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151585 | ||||||
chr2:231151641
|
C | CT | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2116-1920dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151641 | |||||
chr2:231151801
|
GA | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0170others(19): Show | 24 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.2116-1761delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151801 | |||||
chr2:231151803
|
A | AT | 28 | a0001c0001t0001g0168a0001c0001t0001g0219a0001c0001t0001g0225others(25): Show | 28 | HG00438.hp1 HG00673.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2116-1735dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151803 | |||||
chr2:231151803
|
A | T | 9 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0174others(6): Show | 9 | HG00673.hp1 HG01361.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.2116-1761A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151803 | ||||||
chr2:231151803
|
AT | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0086others(103): Show | 110 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2116-1735delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151803 | |||||
chr2:231151803
|
ATT | A | 15 | a0001c0001t0001g0281a0001c0001t0003g0119a0001c0001t0003g0122others(12): Show | 15 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2116-1736_2116-173 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151803 | |||||
chr2:231151831
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2116-1733A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151831 | ||||||
chr2:231152427
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2116-1137G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152427 | ||||||
chr2:231152461
|
C | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-1103C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152461 | ||||||
chr2:231152588
|
C | G | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG00735.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2116-976C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152588 | ||||||
chr2:231152627
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-937A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152627 | ||||||
chr2:231153032
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2116-532G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153032 | ||||||
chr2:231153169
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-395A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153169 | ||||||
chr2:231153170
|
G | T | 1 | a0001c0001t0002g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-394G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153170 | ||||||
chr2:231153171
|
G | T | 1 | a0001c0001t0002g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-393G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153171 | ||||||
chr2:231153193
|
G | A | 2 | a0001c0001t0002g0010a0004c0004t0002g0009 | 2 | NA19003.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2116-371G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153193 | ||||||
chr2:231153540
|
T | C | 1 | a0002c0003t0003g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2116-24T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153540 | ||||||
chr2:231153543
|
T | G | 1 | a0002c0003t0003g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2116-21T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153543 | ||||||
chr2:231153544
|
T | A | 1 | a0002c0003t0003g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2116-20T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153544 | ||||||
chr2:231153794
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+128C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231153794 | ||||||
chr2:231153911
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2218+245C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231153911 | ||||||
chr2:231154003
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2218+337C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154003 | ||||||
chr2:231154070
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2218+404G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154070 | ||||||
chr2:231154074
|
T | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2218+408T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154074 | ||||||
chr2:231154087
|
G | A | 1 | a0001c0002t0004g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2218+421G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154087 | ||||||
chr2:231154105
|
C | T | 6 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.2218+439C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154105 | ||||||
chr2:231154128
|
C | A | 8 | a0001c0001t0001g0022a0001c0001t0002g0074a0001c0002t0004g0023others(5): Show | 8 | HG01516.hp1 HG02280.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2218+462C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154128 | ||||||
chr2:231154265
|
C | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 243 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.2218+599C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154265 | ||||||
chr2:231154375
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2218+709A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154375 | ||||||
chr2:231154455
|
CTGTT | C | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2218+790_2218+793d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154455 | ||||||
chr2:231154575
|
A | C | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2218+909A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154575 | ||||||
chr2:231154655
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+989G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154655 | ||||||
chr2:231155048
|
G | A | 2 | a0001c0002t0004g0024a0001c0002t0004g0025 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2218+1382G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155048 | ||||||
chr2:231155074
|
A | T | 1 | a0001c0001t0001g0175 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2218+1408A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155074 | ||||||
chr2:231155203
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2218+1537G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155203 | ||||||
chr2:231155507
|
TA | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2218+1850delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231155507 | |||||
chr2:231155523
|
T | A | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2218+1857T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155523 | ||||||
chr2:231155587
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2218+1921G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155587 | ||||||
chr2:231155627
|
T | TA | 11 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(8): Show | 11 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2218+1962dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231155627 | |||||
chr2:231155741
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+2075G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155741 | ||||||
chr2:231155887
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2218+2221G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155887 | ||||||
chr2:231156107
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(230): Show | 241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2218+2441T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156107 | ||||||
chr2:231156393
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2218+2727T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156393 | ||||||
chr2:231156430
|
A | G | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2218+2764A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156430 | ||||||
chr2:231156479
|
A | T | 2 | a0001c0001t0001g0251a0001c0001t0003g0166 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2218+2813A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156479 | ||||||
chr2:231156497
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(21): Show | 26 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2218+2831A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156497 | ||||||
chr2:231156547
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+2881T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156547 | ||||||
chr2:231156548
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 240 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2218+2882G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156548 | ||||||
chr2:231156588
|
T | C | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2218+2922T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156588 | ||||||
chr2:231156597
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2218+2931T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156597 | ||||||
chr2:231156640
|
T | C | 7 | a0001c0001t0001g0227a0001c0001t0001g0328a0001c0001t0001g0329others(4): Show | 7 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2218+2974T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156640 | ||||||
chr2:231156700
|
A | G | 7 | a0001c0001t0003g0141a0001c0001t0003g0149a0001c0001t0003g0150others(4): Show | 7 | NA18972.hp1 NA18975.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2218+3034A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156700 | ||||||
chr2:231156725
|
T | C | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2218+3059T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156725 | ||||||
chr2:231156924
|
T | C | 1 | a0002c0003t0002g0079 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2218+3258T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156924 | ||||||
chr2:231157253
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2218+3587G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157253 | ||||||
chr2:231157430
|
C | CT | 10 | a0001c0001t0001g0227a0001c0001t0001g0328a0001c0001t0001g0329others(7): Show | 10 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2218+3779dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231157430 | |||||
chr2:231157434
|
T | C | 1 | a0001c0001t0002g0115 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2218+3768T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157434 | ||||||
chr2:231157441
|
T | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2218+3775T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157441 | ||||||
chr2:231157442
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(28): Show | 33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.2218+3776T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157442 | ||||||
chr2:231157586
|
T | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-3754T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157586 | ||||||
chr2:231157586
|
T | TG | 84 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(81): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2219-3746dupG | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231157586 | |||||
chr2:231157693
|
T | G | 41 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(38): Show | 41 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.2219-3647T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157693 | ||||||
chr2:231157694
|
G | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2219-3646G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157694 | ||||||
chr2:231157976
|
G | C | 1 | a0001c0001t0002g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2219-3364G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157976 | ||||||
chr2:231158218
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(27): Show | 32 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.2219-3122C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158218 | ||||||
chr2:231158246
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-3094G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158246 | ||||||
chr2:231158267
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.2219-3073G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158267 | ||||||
chr2:231158316
|
A | C | 1 | a0001c0001t0001g0302 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2219-3024A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158316 | ||||||
chr2:231158319
|
A | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2219-3021A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158319 | ||||||
chr2:231158569
|
A | G | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2219-2771A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158569 | ||||||
chr2:231158609
|
T | C | 11 | a0001c0001t0001g0233a0001c0001t0003g0117a0001c0001t0003g0118others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2219-2731T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158609 | ||||||
chr2:231158781
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2219-2559G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158781 | ||||||
chr2:231158857
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2219-2483G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158857 | ||||||
chr2:231158961
|
T | C | 1 | a0001c0001t0001g0302 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2219-2379T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158961 | ||||||
chr2:231159281
|
G | A | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2219-2059G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159281 | ||||||
chr2:231159285
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2219-2055G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159285 | ||||||
chr2:231159499
|
A | C | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2219-1841A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159499 | ||||||
chr2:231159823
|
G | T | 1 | a0001c0001t0002g0018 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2219-1517G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159823 | ||||||
chr2:231159845
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2219-1495T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159845 | ||||||
chr2:231159923
|
G | C | 1 | a0001c0001t0001g0302 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2219-1417G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159923 | ||||||
chr2:231159993
|
C | T | 2 | a0001c0002t0004g0023a0001c0002t0004g0027 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2219-1347C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159993 | ||||||
chr2:231160174
|
A | G | 1 | a0001c0001t0003g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2219-1166A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160174 | ||||||
chr2:231160185
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2219-1155A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160185 | ||||||
chr2:231160308
|
A | C | 1 | a0001c0001t0003g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2219-1032A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160308 | ||||||
chr2:231160387
|
G | C | 1 | a0001c0001t0001g0346 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2219-953G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160387 | ||||||
chr2:231160570
|
G | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 311 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.2219-770G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160570 | ||||||
chr2:231160608
|
C | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-732C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160608 | ||||||
chr2:231160919
|
T | C | 2 | a0001c0001t0002g0068a0001c0001t0002g0345 | 2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2219-421T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160919 | ||||||
chr2:231160960
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-380C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160960 | ||||||
chr2:231161001
|
A | G | 1 | a0001c0001t0003g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2219-339A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161001 | ||||||
chr2:231161018
|
C | G | 1 | a0001c0001t0003g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2219-322C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161018 | ||||||
chr2:231161105
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0221a0001c0001t0001g0226 | 3 | NA18947.hp2 NA18950.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.2219-235G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161105 | ||||||
chr2:231161166
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0169others(29): Show | 34 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.2219-174C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161166 | ||||||
chr2:231161177
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2219-163A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161177 | ||||||
chr2:231161238
|
T | TA | 86 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(83): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.2219-88dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231161238 | |||||
chr2:231161280
|
G | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(39): Show | 44 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2219-60G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161280 | ||||||
chr2:231161336
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0096 | 2 | HG00733.hp1 NA20905.hp2 |
splice_region_variant&intron_variant | LOW | c.2219-4A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161336 | ||||||
chr2:231161524
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2388+15C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231161524 | ||||||
chr2:231161552
|
C | T | 2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2388+43C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231161552 | ||||||
chr2:231161553
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2388+44G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231161553 | ||||||
chr2:231162042
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2388+533C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162042 | ||||||
chr2:231162582
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-1053G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162582 | ||||||
chr2:231162599
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-1036G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162599 | ||||||
chr2:231162826
|
C | CA | 13 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(10): Show | 13 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2389-795dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231162826 | |||||
chr2:231162854
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0102 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2389-781A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162854 | ||||||
chr2:231162862
|
C | A | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2389-773C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162862 | ||||||
chr2:231163016
|
C | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-619C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163016 | ||||||
chr2:231163029
|
G | A | 1 | a0001c0002t0004g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2389-606G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163029 | ||||||
chr2:231163056
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-579G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163056 | ||||||
chr2:231163080
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-555A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163080 | ||||||
chr2:231163100
|
C | CA | 89 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(86): Show | 93 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2389-521dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231163100 | |||||
chr2:231163118
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2389-517A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163118 | ||||||
chr2:231163190
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0178a0001c0001t0001g0179others(8): Show | 12 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.2389-445C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163190 | ||||||
chr2:231163207
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2389-428C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163207 | ||||||
chr2:231163292
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2389-343G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163292 | ||||||
chr2:231163865
|
A | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+138A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231163865 | ||||||
chr2:231163870
|
A | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+143A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231163870 | ||||||
chr2:231163986
|
A | G | 10 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0122others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2481+259A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231163986 | ||||||
chr2:231164031
|
T | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+304T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164031 | ||||||
chr2:231164055
|
A | G | 11 | a0001c0001t0002g0064a0001c0001t0003g0117a0001c0001t0003g0118others(8): Show | 11 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2481+328A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164055 | ||||||
chr2:231164086
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2481+359G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164086 | ||||||
chr2:231164441
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2481+714A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164441 | ||||||
chr2:231164484
|
C | CATG | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-714_2482-713i others(5): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231164484 | |||||
chr2:231164579
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2482-621T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164579 | ||||||
chr2:231164589
|
A | G | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(2): Show | 5 | HG00438.hp2 HG02027.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-611A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164589 | ||||||
chr2:231164716
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2482-484G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164716 | ||||||
chr2:231164783
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-417G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164783 | ||||||
chr2:231164784
|
C | T | 1 | a0001c0001t0002g0345 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2482-416C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164784 | ||||||
chr2:231164854
|
A | G | 48 | a0001c0001t0001g0248a0001c0001t0001g0281a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2482-346A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164854 | ||||||
chr2:231164885
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2482-315C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164885 | ||||||
chr2:231164890
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-310G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164890 | ||||||
chr2:231165021
|
GATTTATA others(3): Show |
G | 4 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0168others(1): Show | 6 | HG02027.hp2 HG03195.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-166_2482-157d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165021 | |||||
chr2:231165023
|
TTTATATA others(28): Show |
T | 2 | a0001c0001t0001g0194a0001c0001t0001g0284 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2482-175_2482-141d others(37): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165023 | |||||
chr2:231165024
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2482-176T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165024 | ||||||
chr2:231165024
|
T | TTA | 3 | a0001c0001t0001g0212a0001c0001t0001g0297a0001c0001t0001g0322 | 3 | HG02683.hp2 NA18952.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2482-168_2482-167d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
T | TTATA | 3 | a0001c0001t0001g0173a0001c0001t0001g0191a0001c0001t0003g0344 | 3 | HG02965.hp2 NA18968.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2482-170_2482-167d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(5): Show |
T | 4 | a0001c0001t0001g0321a0001c0001t0003g0122a0001c0001t0003g0123others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-166_2482-155d others(14): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(7): Show |
T | 4 | a0001c0001t0001g0220a0001c0001t0001g0232a0001c0001t0001g0292others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-166_2482-153d others(16): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0222a0001c0001t0003g0117a0001c0001t0003g0118others(1): Show | 4 | HG03209.hp1 HG03540.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-166_2482-151d others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0001g0335 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2482-166_2482-149d others(20): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(13): Show |
T | 2 | a0001c0001t0002g0014a0001c0001t0002g0016 | 2 | NA19062.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2482-166_2482-147d others(22): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(15): Show |
T | 1 | a0001c0001t0001g0306 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2482-166_2482-145d others(24): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(17): Show |
T | 1 | a0001c0001t0001g0320 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2482-166_2482-143d others(26): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(19): Show |
T | 7 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0186others(4): Show | 7 | HG00408.hp1 HG00673.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.2482-166_2482-141d others(28): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(21): Show |
T | 8 | a0001c0001t0001g0225a0001c0001t0001g0294a0001c0001t0001g0295others(5): Show | 8 | HG00423.hp1 HG00673.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-166_2482-139d others(30): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(23): Show |
T | 1 | a0001c0001t0001g0330 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2482-166_2482-137d others(32): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(25): Show |
T | 16 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(13): Show | 16 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.2482-166_2482-135d others(34): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(27): Show |
T | 6 | a0001c0001t0001g0250a0001c0001t0001g0264a0001c0001t0001g0287others(3): Show | 6 | HG01109.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-166_2482-133d others(36): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(29): Show |
T | 15 | a0001c0001t0001g0229a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 15 | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2482-166_2482-131d others(38): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(31): Show |
T | 65 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(62): Show | 67 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.2482-166_2482-129d others(40): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(35): Show |
T | 3 | a0001c0001t0001g0022a0001c0001t0001g0175a0001c0001t0001g0314 | 3 | HG03710.hp2 NA18942.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2482-166_2482-125d others(44): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(37): Show |
T | 6 | a0001c0001t0001g0021a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-166_2482-123d others(46): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(45): Show |
T | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-166_2482-115d others(54): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165024
|
TTATATAT others(47): Show |
T | 48 | a0001c0001t0001g0248a0001c0001t0001g0281a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2482-166_2482-113d others(56): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | |||||
chr2:231165026
|
ATATATAT others(1): Show |
A | 8 | a0001c0001t0001g0008a0001c0001t0001g0213a0001c0001t0001g0214others(5): Show | 9 | HG01981.hp1 HG02129.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-166_2482-159d others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165026 | |||||
chr2:231165028
|
A | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | NA18947.hp2 NA18971.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-172A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165028 | ||||||
chr2:231165028
|
ATATATT | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0303 | 3 | HG02056.hp1 NA18975.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2482-166_2482-161d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165028 | |||||
chr2:231165030
|
ATATT | A | 8 | a0001c0001t0001g0169a0001c0001t0001g0187a0001c0001t0001g0189others(5): Show | 8 | HG02451.hp2 HG03579.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2482-166_2482-163d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165030 | |||||
chr2:231165032
|
ATT | A | 8 | a0001c0001t0001g0172a0001c0001t0001g0211a0001c0001t0001g0216others(5): Show | 8 | HG01123.hp1 HG03927.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-166_2482-165d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165032 | |||||
chr2:231165034
|
T | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0171others(23): Show | 27 | HG00609.hp1 HG00639.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2482-166T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165034 | ||||||
chr2:231165034
|
T | TTA | 10 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0039others(7): Show | 10 | HG02523.hp2 HG03942.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.2482-110_2482-109d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
T | TTATA | 8 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0044others(5): Show | 8 | HG02109.hp1 HG04228.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-112_2482-109d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
T | TTATATA | 4 | a0001c0001t0002g0013a0001c0001t0002g0064a0001c0001t0002g0074others(1): Show | 4 | HG01081.hp1 HG01516.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-114_2482-109d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0002g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2482-118_2482-109d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTA | T | 14 | a0001c0001t0002g0020a0001c0001t0002g0037a0001c0001t0002g0049others(11): Show | 14 | HG01074.hp1 HG01515.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.2482-110_2482-109d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATA | T | 14 | a0001c0001t0002g0010a0001c0001t0002g0036a0001c0001t0002g0045others(11): Show | 14 | HG00438.hp2 HG00639.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2482-112_2482-109d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATA | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0035a0001c0001t0002g0041others(12): Show | 16 | HG00323.hp1 HG00609.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2482-114_2482-109d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATAT others(1): Show |
T | 3 | a0001c0001t0002g0058a0001c0001t0002g0073a0001c0001t0002g0109 | 3 | HG01168.hp2 HG01884.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.2482-116_2482-109d others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATAT others(3): Show |
T | 2 | a0001c0001t0002g0029a0001c0001t0002g0067 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2482-118_2482-109d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATAT others(9): Show |
T | 4 | a0001c0001t0002g0033a0001c0001t0002g0065a0001c0001t0002g0095others(1): Show | 4 | HG01981.hp2 HG02300.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-124_2482-109d others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0002g0107 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2482-128_2482-109d others(22): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2482-134_2482-109d others(28): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATAT others(23): Show |
T | 3 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0102 | 3 | HG01243.hp2 NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2482-138_2482-109d others(32): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165034
|
TTATATAT others(33): Show |
T | 1 | a0001c0001t0002g0115 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2482-148_2482-109d others(42): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | |||||
chr2:231165036
|
A | T | 2 | a0001c0001t0002g0077a0001c0001t0002g0092 | 2 | HG00735.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2482-164A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165036 | ||||||
chr2:231165038
|
A | T | 2 | a0001c0001t0001g0321a0001c0001t0002g0108 | 2 | NA18957.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2482-162A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165038 | ||||||
chr2:231165040
|
A | T | 1 | a0001c0001t0002g0075 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2482-160A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165040 | ||||||
chr2:231165042
|
A | T | 2 | a0001c0001t0001g0220a0001c0001t0002g0041 | 2 | HG00323.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2482-158A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165042 | ||||||
chr2:231165044
|
A | T | 2 | a0001c0001t0001g0222a0001c0001t0002g0073 | 2 | HG01168.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2482-156A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165044 | ||||||
chr2:231165048
|
A | ACAATATA others(19): Show |
1 | a0001c0001t0002g0104 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-152_2482-151i others(28): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165048 | ||||||
chr2:231165052
|
A | T | 2 | a0001c0001t0002g0095a0001c0001t0002g0105 | 2 | HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2482-148A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165052 | ||||||
chr2:231165056
|
A | T | 1 | a0001c0001t0002g0104 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-144A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165056 | ||||||
chr2:231165063
|
T | C | 2 | a0001c0001t0002g0104a0001c0001t0002g0107 | 2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2482-137T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165063 | ||||||
chr2:231165070
|
A | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-130A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165070 | ||||||
chr2:231165071
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-129T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165071 | ||||||
chr2:231165079
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-121T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165079 | ||||||
chr2:231165082
|
A | G | 4 | a0001c0001t0001g0232a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-118A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165082 | ||||||
chr2:231165088
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0096 | 2 | HG00733.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2482-112A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165088 | ||||||
chr2:231165191
|
T | C | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-9T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165191 | ||||||
chr2:231165448
|
C | CTA | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2568+162_2568+163i others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165448 | ||||||
chr2:231165587
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(230): Show | 241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2569-284C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165587 | ||||||
chr2:231165796
|
C | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.2569-75C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165796 | ||||||
chr2:231165841
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2569-30G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165841 | ||||||
chr2:231166147
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 242 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.2715+130A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166147 | ||||||
chr2:231166176
|
A | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0289 | 2 | NA19076.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2715+159A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166176 | ||||||
chr2:231166503
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(69): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2715+486G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166503 | ||||||
chr2:231166508
|
C | CT | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 236 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.2715+503dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231166508 | |||||
chr2:231166642
|
G | A | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+625G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166642 | ||||||
chr2:231166691
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+674C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166691 | ||||||
chr2:231166886
|
C | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+869C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166886 | ||||||
chr2:231167020
|
T | A | 1 | a0001c0001t0001g0266 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2715+1003T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167020 | ||||||
chr2:231167134
|
G | A | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+1117G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167134 | ||||||
chr2:231167387
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2715+1370G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167387 | ||||||
chr2:231167491
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2715+1474T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167491 | ||||||
chr2:231168134
|
C | T | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+2117C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168134 | ||||||
chr2:231168150
|
C | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02258.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2715+2133C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168150 | ||||||
chr2:231168307
|
T | G | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2716-2259T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168307 | ||||||
chr2:231168361
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG01243.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2716-2205G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168361 | ||||||
chr2:231168578
|
T | A | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2716-1988T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168578 | ||||||
chr2:231168615
|
G | A | 1 | a0001c0001t0002g0082 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2716-1951G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168615 | ||||||
chr2:231168688
|
T | C | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2716-1878T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168688 | ||||||
chr2:231168760
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2716-1806A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168760 | ||||||
chr2:231168836
|
G | T | 1 | a0001c0001t0006g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2716-1730G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168836 | ||||||
chr2:231169060
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2716-1506T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169060 | ||||||
chr2:231169087
|
A | AC | 75 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0168others(72): Show | 77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2716-1477dupC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231169087 | |||||
chr2:231169159
|
T | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0230a0001c0001t0001g0231others(8): Show | 11 | HG02080.hp1 HG02738.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.2716-1407T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169159 | ||||||
chr2:231169563
|
T | C | 2 | a0001c0001t0001g0022a0001c0005t0001g0028 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2716-1003T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169563 | ||||||
chr2:231169628
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.2716-938C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169628 | ||||||
chr2:231170801
|
G | A | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*9+80G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231170801 | ||||||
chr2:231170820
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.*9+99T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231170820 | ||||||
chr2:231170929
|
C | G | 5 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.*9+208C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231170929 | ||||||
chr2:231171013
|
C | T | 1 | a0001c0001t0001g0007 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.*9+292C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171013 | ||||||
chr2:231171079
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.*9+358C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171079 | ||||||
chr2:231171138
|
C | G | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.*9+417C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171138 | ||||||
chr2:231171549
|
A | AT | 92 | a0001c0001t0001g0007a0001c0001t0001g0197a0001c0001t0001g0207others(89): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.*9+851dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr2 | 231171549 | |||||
chr2:231171549
|
A | ATT | 15 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0168others(12): Show | 16 | HG00558.hp1 HG02027.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.*9+850_*9+851dupTT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr2 | 231171549 | |||||
chr2:231171549
|
AT | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(31): Show | 36 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.*9+851delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr2 | 231171549 | |||||
chr2:231171634
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*10-901G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171634 | ||||||
chr2:231171660
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*10-875G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171660 | ||||||
chr2:231171682
|
G | A | 48 | a0001c0001t0001g0248a0001c0001t0001g0281a0001c0001t0003g0003others(45): Show | 50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.*10-853G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171682 | ||||||
chr2:231171808
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*10-727G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171808 | ||||||
chr2:231171853
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038 | 3 | HG01074.hp1 HG04204.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.*10-682G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171853 | ||||||
chr2:231171869
|
C | A | 2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*10-666C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171869 | ||||||
chr2:231171947
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*10-588C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171947 | ||||||
chr2:231172129
|
T | G | 43 | a0001c0001t0001g0248a0001c0001t0001g0281a0001c0001t0003g0003others(40): Show | 45 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.*10-406T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172129 | ||||||
chr2:231172169
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0130others(79): Show | 84 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.*10-366G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172169 | ||||||
chr2:231172242
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*10-293A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172242 | ||||||
chr2:231172280
|
A | G | 1 | a0001c0001t0002g0104 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.*10-255A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172280 | ||||||
chr2:231172315
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G | T | 1 | a0001c0001t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.*10-220G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172315 | ||||||
chr2:231172353
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T | C | 1 | a0001c0005t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*10-182T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172353 |