geneid | 10213 |
---|---|
ensemblid | ENSG00000115233.12 |
hgncid | 16889 |
symbol | PSMD14 |
name | proteasome 26S subunit, non-ATPase 14 |
refseq_nuc | NM_005805.6 |
refseq_prot | NP_005796.1 |
ensembl_nuc | ENST00000409682.8 |
ensembl_prot | ENSP00000386541.3 |
mane_status | MANE Select |
chr | chr2 |
start | 161308425 |
end | 161411717 |
strand | + |
ver | v1.2 |
region | chr2:161308425-161411717 |
region5000 | chr2:161303425-161416717 |
regionname0 | PSMD14_chr2_161308425_161411717 |
regionname5000 | PSMD14_chr2_161303425_161416717 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 310 | 268 | 72 | 34 | 116 | 12 | 32 | 86 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 933 | 268 | 72 | 34 | 116 | 12 | 32 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 635 | 138 | 29 | 14 | 67 | 5 | 22 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
t0002 | 0/1 | 635 | 124 | 42 | 16 | 49 | 7 | 9 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
t0003 | 0/0 | 635 | 5 | 0 | 4 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
t0004 | 0/0 | 635 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 933 | 268 | 72 | 34 | 116 | 12 | 32 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1567 | 138 | 29 | 14 | 67 | 5 | 22 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
a0001c0001t0002 | 0/1 | 1567 | 124 | 42 | 16 | 49 | 7 | 9 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
a0001c0001t0003 | 0/0 | 1567 | 5 | 0 | 4 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
a0001c0001t0004 | 0/0 | 1567 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | copy fasta | chr2 | 161303425 | 161416717 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | GBR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ASW | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ASW | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | TSI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0055 | REF | REF | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0192 | REF | REF | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:161308497
|
A | T | 2 | a0001c0001t0002a0001c0001t0003 | 129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-245A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/12 | chr2 | 161308497 | ||||||
chr2:161316504
|
A | T | 1 | a0001c0001t0004 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/12 | 2322 | chr2 | 161316504 | |||||
chr2:161411597
|
G | A | 1 | a0001c0001t0003 | 5 | HG00735.hp1 HG01123.hp1 HG01496.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*197G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 12/12 | 197 | chr2 | 161411597 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:161308932
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-138+328G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161308932 | ||||||
chr2:161309052
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-138+448G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161309052 | ||||||
chr2:161309549
|
AAC | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG00423.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.-138+949_-138+950d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 161309549 | |||||
chr2:161309640
|
A | C | 71 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(68): Show | 73 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-138+1036A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161309640 | ||||||
chr2:161309934
|
T | A | 1 | a0001c0001t0002g0009 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-138+1330T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161309934 | ||||||
chr2:161310034
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-138+1430G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161310034 | ||||||
chr2:161310101
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-138+1497A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161310101 | ||||||
chr2:161310476
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-138+1872G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161310476 | ||||||
chr2:161310502
|
G | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.-138+1898G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161310502 | ||||||
chr2:161310560
|
TTAAA | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG00735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-138+1960_-138+196 others(8): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 161310560 | |||||
chr2:161310918
|
A | G | 1 | a0001c0001t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-138+2314A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161310918 | ||||||
chr2:161310967
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-138+2363C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161310967 | ||||||
chr2:161311171
|
T | C | 110 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(107): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-138+2567T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161311171 | ||||||
chr2:161311178
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-138+2574G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161311178 | ||||||
chr2:161311266
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-138+2662G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161311266 | ||||||
chr2:161311588
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-138+2984A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161311588 | ||||||
chr2:161311625
|
C | CT | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0193others(9): Show | 14 | HG00423.hp1 HG02698.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-138+3045dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 161311625 | |||||
chr2:161311625
|
CT | C | 176 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0117others(173): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-138+3045delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 161311625 | |||||
chr2:161311625
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0196 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-138+3032_-138+304 others(18): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 161311625 | |||||
chr2:161311775
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-138+3171C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161311775 | ||||||
chr2:161312196
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-138+3592T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312196 | ||||||
chr2:161312206
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-138+3602C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312206 | ||||||
chr2:161312431
|
A | C | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-138+3827A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312431 | ||||||
chr2:161312523
|
A | G | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(2): Show | 5 | HG02280.hp2 NA18522.hp1 NA20129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137-3914A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312523 | ||||||
chr2:161312540
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-137-3897A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312540 | ||||||
chr2:161312613
|
C | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(60): Show | 65 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-137-3824C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312613 | ||||||
chr2:161312848
|
C | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(1): Show | 4 | HG00423.hp2 HG02056.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137-3589C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312848 | ||||||
chr2:161312971
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG00741.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-137-3466G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312971 | ||||||
chr2:161312995
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-137-3442G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161312995 | ||||||
chr2:161313120
|
T | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-137-3317T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313120 | ||||||
chr2:161313203
|
C | T | 1 | a0001c0001t0003g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-137-3234C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313203 | ||||||
chr2:161313283
|
A | T | 1 | a0001c0001t0002g0109 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-137-3154A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313283 | ||||||
chr2:161313357
|
T | A | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-137-3080T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313357 | ||||||
chr2:161313598
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0251 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-137-2839C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313598 | ||||||
chr2:161313918
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-137-2519T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313918 | ||||||
chr2:161313941
|
T | C | 1 | a0001c0001t0002g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-137-2496T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313941 | ||||||
chr2:161313952
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-137-2485C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161313952 | ||||||
chr2:161314533
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-137-1904G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161314533 | ||||||
chr2:161314666
|
C | G | 1 | a0001c0001t0004g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137-1771C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161314666 | ||||||
chr2:161314761
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0004g0165 | 2 | HG02055.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-137-1676A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161314761 | ||||||
chr2:161314780
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-137-1657T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161314780 | ||||||
chr2:161315085
|
C | G | 20 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(17): Show | 20 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.-137-1352C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161315085 | ||||||
chr2:161315333
|
T | G | 16 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(13): Show | 16 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-137-1104T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161315333 | ||||||
chr2:161315397
|
G | A | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | NA18979.hp1 NA18994.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137-1040G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161315397 | ||||||
chr2:161315501
|
G | T | 76 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(73): Show | 76 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-137-936G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161315501 | ||||||
chr2:161315611
|
T | A | 10 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(7): Show | 10 | HG02145.hp2 HG02809.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137-826T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161315611 | ||||||
chr2:161315841
|
CT | C | 232 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(229): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-137-577delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 161315841 | |||||
chr2:161315892
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-137-545G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161315892 | ||||||
chr2:161316000
|
C | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | NA18948.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-137-437C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161316000 | ||||||
chr2:161316293
|
A | G | 2 | a0001c0001t0002g0031a0001c0001t0002g0112 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-137-144A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 1/11 | chr2 | 161316293 | ||||||
chr2:161316611
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0001g0144others(11): Show | 14 | HG00438.hp2 HG02015.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5+42C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161316611 | ||||||
chr2:161316659
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | NA18979.hp1 NA18994.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+90C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161316659 | ||||||
chr2:161316797
|
G | T | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG02886.hp2 HG03139.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+228G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161316797 | ||||||
chr2:161316867
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+298T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161316867 | ||||||
chr2:161316918
|
T | A | 1 | a0001c0001t0002g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-5+349T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161316918 | ||||||
chr2:161316965
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-5+396A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161316965 | ||||||
chr2:161317260
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-5+691C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161317260 | ||||||
chr2:161317267
|
T | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 77 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-5+698T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161317267 | ||||||
chr2:161317846
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-4-976T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161317846 | ||||||
chr2:161318062
|
C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-4-760C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161318062 | ||||||
chr2:161318326
|
A | G | 10 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-496A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161318326 | ||||||
chr2:161318383
|
A | C | 1 | a0001c0001t0001g0260 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-4-439A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161318383 | ||||||
chr2:161318502
|
C | T | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA20129.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4-320C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161318502 | ||||||
chr2:161318779
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-4-43T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 2/11 | chr2 | 161318779 | ||||||
chr2:161319035
|
CAT | C | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+163_48+164delAT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161319035 | ||||||
chr2:161319340
|
ATCTC | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+472_48+475delTC others(2): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161319340 | |||||
chr2:161319390
|
A | C | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.48+517A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161319390 | ||||||
chr2:161319533
|
C | T | 192 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0117others(189): Show | 193 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.48+660C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161319533 | ||||||
chr2:161319728
|
T | G | 6 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 6 | HG02886.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+855T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161319728 | ||||||
chr2:161319765
|
T | A | 1 | a0001c0001t0002g0168 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.48+892T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161319765 | ||||||
chr2:161320179
|
G | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+1306G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161320179 | ||||||
chr2:161320927
|
T | C | 1 | a0001c0001t0002g0055 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.48+2054T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161320927 | ||||||
chr2:161320973
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.48+2100G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161320973 | ||||||
chr2:161320987
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.48+2114A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161320987 | ||||||
chr2:161322682
|
G | A | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.48+3809G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161322682 | ||||||
chr2:161322686
|
G | A | 47 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(44): Show | 47 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.48+3813G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161322686 | ||||||
chr2:161323068
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+4195T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161323068 | ||||||
chr2:161323107
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.48+4234C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161323107 | ||||||
chr2:161323567
|
G | A | 4 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01192.hp2 NA19004.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+4694G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161323567 | ||||||
chr2:161323584
|
ACCCAGGA others(4): Show |
A | 1 | a0001c0001t0002g0104 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.48+4712_48+4722del others(11): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161323584 | ||||||
chr2:161323712
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.48+4839A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161323712 | ||||||
chr2:161323940
|
C | CA | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+5069dupA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161323940 | |||||
chr2:161323974
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.48+5101C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161323974 | ||||||
chr2:161324234
|
A | G | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | NA18950.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.48+5361A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324234 | ||||||
chr2:161324285
|
T | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0258 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.48+5412T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324285 | ||||||
chr2:161324606
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.48+5733G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324606 | ||||||
chr2:161324624
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.48+5751T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324624 | ||||||
chr2:161324632
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.48+5759T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324632 | ||||||
chr2:161324633
|
C | CT | 7 | a0001c0001t0001g0007a0001c0001t0002g0101a0001c0001t0002g0152others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+5774dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161324633 | |||||
chr2:161324697
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.48+5824G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324697 | ||||||
chr2:161324814
|
A | G | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA20129.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.48+5941A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324814 | ||||||
chr2:161324931
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.48+6058G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161324931 | ||||||
chr2:161325276
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(60): Show | 65 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.48+6403T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161325276 | ||||||
chr2:161325389
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.48+6516A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161325389 | ||||||
chr2:161325543
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.48+6670T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161325543 | ||||||
chr2:161325850
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.48+6977A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161325850 | ||||||
chr2:161326156
|
G | C | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA20129.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.48+7283G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326156 | ||||||
chr2:161326290
|
G | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+7417G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326290 | ||||||
chr2:161326327
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.48+7454A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326327 | ||||||
chr2:161326443
|
G | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+7570G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326443 | ||||||
chr2:161326454
|
G | A | 6 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(3): Show | 6 | HG02630.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+7581G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326454 | ||||||
chr2:161326584
|
C | A | 1 | a0001c0001t0002g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.48+7711C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326584 | ||||||
chr2:161326592
|
T | G | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA20129.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.48+7719T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326592 | ||||||
chr2:161326996
|
T | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.48+8123T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326996 | ||||||
chr2:161327019
|
T | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.48+8146T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327019 | ||||||
chr2:161327400
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.48+8527A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327400 | ||||||
chr2:161327527
|
C | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.48+8654C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327527 | ||||||
chr2:161327810
|
G | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+8937G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327810 | ||||||
chr2:161327878
|
T | TA | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(60): Show | 65 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.48+9011dupA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327878 | |||||
chr2:161327885
|
C | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+9012C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327885 | ||||||
chr2:161327914
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 5 | NA18954.hp2 NA18979.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+9041G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327914 | ||||||
chr2:161327946
|
C | CTG | 6 | a0001c0001t0001g0007a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01109.hp1 HG03098.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+9110_48+9111dup others(2): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTG | 32 | a0001c0001t0001g0010a0001c0001t0001g0118a0001c0001t0001g0119others(29): Show | 32 | HG00438.hp2 HG01978.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.48+9108_48+9111dup others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTG | 26 | a0001c0001t0001g0117a0001c0001t0001g0131a0001c0001t0001g0134others(23): Show | 26 | HG00438.hp1 HG00673.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.48+9106_48+9111dup others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(1): Show |
41 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0132others(38): Show | 42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.48+9104_48+9111dup others(8): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(3): Show |
29 | a0001c0001t0001g0006a0001c0001t0001g0141a0001c0001t0001g0142others(26): Show | 30 | HG00140.hp1 HG00423.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.48+9102_48+9111dup others(10): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(5): Show |
14 | a0001c0001t0001g0209a0001c0001t0001g0225a0001c0001t0001g0246others(11): Show | 15 | HG00609.hp2 HG01515.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.48+9100_48+9111dup others(12): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(7): Show |
11 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0002g0024others(8): Show | 11 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.48+9098_48+9111dup others(14): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(9): Show |
26 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(23): Show | 26 | HG00544.hp2 HG00621.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.48+9096_48+9111dup others(16): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(11): Show |
17 | a0001c0001t0001g0204a0001c0001t0002g0013a0001c0001t0002g0020others(14): Show | 17 | HG00323.hp1 HG00423.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.48+9094_48+9111dup others(18): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(13): Show |
11 | a0001c0001t0002g0012a0001c0001t0002g0021a0001c0001t0002g0022others(8): Show | 11 | HG02056.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+9092_48+9111dup others(20): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(15): Show |
6 | a0001c0001t0001g0202a0001c0001t0002g0014a0001c0001t0002g0063others(3): Show | 6 | HG02897.hp1 NA18906.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+9090_48+9111dup others(22): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(17): Show |
4 | a0001c0001t0002g0015a0001c0001t0002g0095a0001c0001t0002g0096others(1): Show | 4 | HG01123.hp1 NA19058.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+9088_48+9111dup others(24): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(19): Show |
4 | a0001c0001t0002g0057a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG00673.hp2 HG02132.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+9086_48+9111dup others(26): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(21): Show |
1 | a0001c0001t0002g0100 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.48+9084_48+9111dup others(28): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
C | CTGTGTGT others(23): Show |
1 | a0001c0001t0002g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.48+9082_48+9111dup others(30): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327946
|
CTGTGTGT others(1): Show |
C | 10 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(7): Show | 10 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+9104_48+9111del others(8): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327946 | |||||
chr2:161327975
|
TGTGTGTG others(3): Show |
T | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | NA18950.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.48+9104_48+9113del others(10): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327975 | |||||
chr2:161327981
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0002g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.48+9111_48+9112ins others(18): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327981 | |||||
chr2:161327981
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0002g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.48+9111_48+9112ins others(22): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161327981 | |||||
chr2:161327985
|
A | T | 108 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(105): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.48+9112A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327985 | ||||||
chr2:161328007
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0193a0001c0001t0001g0194 | 4 | HG02683.hp2 HG02738.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+9134C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161328007 | ||||||
chr2:161328202
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.48+9329G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161328202 | ||||||
chr2:161329047
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+10174C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161329047 | ||||||
chr2:161329389
|
A | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0252 | 3 | HG02056.hp2 HG02132.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.48+10516A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161329389 | ||||||
chr2:161329653
|
A | G | 10 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(7): Show | 10 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+10780A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161329653 | ||||||
chr2:161329903
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48+11030G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161329903 | ||||||
chr2:161330093
|
GATAA | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(59): Show | 64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.48+11227_48+11230d others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161330093 | |||||
chr2:161330098
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.48+11225A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161330098 | ||||||
chr2:161330099
|
T | C | 184 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0117others(181): Show | 185 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.48+11226T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161330099 | ||||||
chr2:161330283
|
C | T | 8 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(5): Show | 8 | HG02040.hp2 HG02080.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+11410C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161330283 | ||||||
chr2:161330306
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48+11433G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161330306 | ||||||
chr2:161330673
|
T | C | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.48+11800T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161330673 | ||||||
chr2:161330739
|
C | T | 72 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(69): Show | 72 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.48+11866C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161330739 | ||||||
chr2:161330922
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02080.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.48+12049A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161330922 | ||||||
chr2:161331208
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+12335T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161331208 | ||||||
chr2:161331258
|
A | AT | 45 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(42): Show | 45 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.48+12401dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161331258 | |||||
chr2:161331266
|
T | A | 3 | a0001c0001t0002g0152a0001c0001t0002g0163a0001c0001t0002g0167 | 3 | HG02280.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.48+12393T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161331266 | ||||||
chr2:161331267
|
T | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA19004.hp2 NA19056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.48+12394T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161331267 | ||||||
chr2:161331275
|
A | T | 2 | a0001c0001t0001g0260a0001c0001t0002g0106 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.48+12402A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161331275 | ||||||
chr2:161331289
|
G | A | 18 | a0001c0001t0002g0001a0001c0001t0002g0018a0001c0001t0002g0032others(15): Show | 19 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.48+12416G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161331289 | ||||||
chr2:161331923
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.48+13050C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161331923 | ||||||
chr2:161332061
|
A | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.48+13188A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161332061 | ||||||
chr2:161332115
|
T | C | 4 | a0001c0001t0002g0079a0001c0001t0002g0095a0001c0001t0002g0100others(1): Show | 4 | NA19057.hp2 NA19058.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+13242T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161332115 | ||||||
chr2:161332139
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.48+13266G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161332139 | ||||||
chr2:161332326
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.48+13453C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161332326 | ||||||
chr2:161332335
|
T | C | 4 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0093others(1): Show | 4 | NA18975.hp2 NA18992.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13462T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161332335 | ||||||
chr2:161332631
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.48+13758G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161332631 | ||||||
chr2:161332745
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.48+13872G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161332745 | ||||||
chr2:161333140
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 5 | NA18954.hp2 NA18979.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+14267G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333140 | ||||||
chr2:161333182
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.48+14309T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333182 | ||||||
chr2:161333595
|
T | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG00544.hp1 HG02074.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+14722T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333595 | ||||||
chr2:161333597
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.48+14724A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333597 | ||||||
chr2:161333674
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.48+14801C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333674 | ||||||
chr2:161333808
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.48+14935G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333808 | ||||||
chr2:161333867
|
C | T | 2 | a0001c0001t0002g0087a0001c0001t0002g0088 | 2 | HG02040.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.48+14994C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333867 | ||||||
chr2:161333926
|
T | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+15053T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161333926 | ||||||
chr2:161334057
|
G | T | 7 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0040others(4): Show | 7 | HG00741.hp2 HG01192.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+15184G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334057 | ||||||
chr2:161334399
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.48+15526C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334399 | ||||||
chr2:161334531
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.48+15658G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334531 | ||||||
chr2:161334648
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.48+15775G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334648 | ||||||
chr2:161334707
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG02257.hp2 HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.48+15834G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334707 | ||||||
chr2:161334713
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.48+15840T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334713 | ||||||
chr2:161334730
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.48+15857A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334730 | ||||||
chr2:161334894
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48+16021T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161334894 | ||||||
chr2:161335468
|
G | T | 5 | a0001c0001t0002g0164a0001c0001t0002g0166a0001c0001t0002g0168others(2): Show | 5 | HG02280.hp1 NA18522.hp1 NA20129.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+16595G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161335468 | ||||||
chr2:161335541
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.48+16668T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161335541 | ||||||
chr2:161335696
|
C | T | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG02886.hp2 HG03139.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+16823C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161335696 | ||||||
chr2:161335777
|
T | C | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.48+16904T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161335777 | ||||||
chr2:161335800
|
G | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02135.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.48+16927G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161335800 | ||||||
chr2:161336110
|
ATGGTCTC others(15): Show |
A | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.48+17283_48+17304d others(24): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161336110 | |||||
chr2:161336255
|
A | C | 4 | a0001c0001t0002g0079a0001c0001t0002g0095a0001c0001t0002g0100others(1): Show | 4 | NA19057.hp2 NA19058.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+17382A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161336255 | ||||||
chr2:161336370
|
A | G | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+17497A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161336370 | ||||||
chr2:161336398
|
G | A | 253 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.48+17525G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161336398 | ||||||
chr2:161336421
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA19004.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.48+17548G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161336421 | ||||||
chr2:161336727
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+17854C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161336727 | ||||||
chr2:161336814
|
G | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.48+17941G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161336814 | ||||||
chr2:161337020
|
A | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0099 | 2 | HG02132.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.48+18147A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161337020 | ||||||
chr2:161337306
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.48+18433T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161337306 | ||||||
chr2:161337430
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.48+18557A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161337430 | ||||||
chr2:161337454
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48+18581C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161337454 | ||||||
chr2:161337463
|
G | C | 1 | a0001c0001t0001g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.48+18590G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161337463 | ||||||
chr2:161337530
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+18657T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161337530 | ||||||
chr2:161337546
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.48+18673C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161337546 | ||||||
chr2:161338203
|
C | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+19330C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161338203 | ||||||
chr2:161338341
|
GTT | G | 243 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(240): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.48+19484_48+19485d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161338341 | |||||
chr2:161338422
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.48+19549C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161338422 | ||||||
chr2:161338900
|
A | G | 10 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(7): Show | 10 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+20027A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161338900 | ||||||
chr2:161339496
|
A | AT | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 72 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.48+20644dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161339496 | |||||
chr2:161339496
|
AT | A | 140 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(137): Show | 141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.48+20644delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161339496 | |||||
chr2:161339496
|
ATT | A | 10 | a0001c0001t0001g0133a0001c0001t0001g0146a0001c0001t0002g0024others(7): Show | 10 | HG01891.hp1 HG01952.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+20643_48+20644d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161339496 | |||||
chr2:161339613
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.48+20740G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161339613 | ||||||
chr2:161339748
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02040.hp2 HG02080.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+20875A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161339748 | ||||||
chr2:161340115
|
G | C | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.48+21242G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340115 | ||||||
chr2:161340117
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.48+21244G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340117 | ||||||
chr2:161340154
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48+21281G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340154 | ||||||
chr2:161340276
|
C | T | 18 | a0001c0001t0002g0054a0001c0001t0002g0070a0001c0001t0002g0077others(15): Show | 18 | HG00621.hp2 HG01928.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.48+21403C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340276 | ||||||
chr2:161340316
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.48+21443G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340316 | ||||||
chr2:161340464
|
A | T | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.48+21591A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340464 | ||||||
chr2:161340634
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.48+21761T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340634 | ||||||
chr2:161340650
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.48+21777C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161340650 | ||||||
chr2:161341023
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.48+22150G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341023 | ||||||
chr2:161341044
|
G | C | 1 | a0001c0001t0001g0202 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.48+22171G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341044 | ||||||
chr2:161341104
|
C | G | 2 | a0001c0001t0002g0045a0001c0001t0002g0051 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.48+22231C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341104 | ||||||
chr2:161341187
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.48+22314G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341187 | ||||||
chr2:161341223
|
G | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.48+22350G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341223 | ||||||
chr2:161341423
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA19004.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.48+22550C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341423 | ||||||
chr2:161341728
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.48+22855A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341728 | ||||||
chr2:161341862
|
TA | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0218others(1): Show | 4 | HG00423.hp1 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+22997delA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161341862 | |||||
chr2:161341869
|
A | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0166 | 2 | NA18522.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.48+22996A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341869 | ||||||
chr2:161341870
|
AT | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 73 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.48+22998delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341870 | ||||||
chr2:161341871
|
T | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0135others(2): Show | 5 | HG01109.hp2 HG01891.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+22998T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341871 | ||||||
chr2:161341873
|
T | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0257 | 2 | HG03516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.48+23000T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341873 | ||||||
chr2:161341875
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.48+23002T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341875 | ||||||
chr2:161341876
|
ATG | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+23005_48+23006d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161341876 | |||||
chr2:161341878
|
G | A | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.48+23005G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161341878 | ||||||
chr2:161342333
|
C | CT | 45 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(42): Show | 45 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.48+23471dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161342333 | |||||
chr2:161342477
|
T | A | 1 | a0001c0001t0001g0236 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.48+23604T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161342477 | ||||||
chr2:161342482
|
T | C | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.48+23609T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161342482 | ||||||
chr2:161342631
|
A | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0049others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+23758A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161342631 | ||||||
chr2:161342705
|
G | A | 4 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01192.hp2 NA19004.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+23832G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161342705 | ||||||
chr2:161343060
|
T | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0167 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.48+24187T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161343060 | ||||||
chr2:161343160
|
T | G | 1 | a0001c0001t0002g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.48+24287T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161343160 | ||||||
chr2:161343317
|
A | G | 4 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-24161A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161343317 | ||||||
chr2:161343340
|
C | G | 4 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0161others(1): Show | 4 | HG00639.hp2 HG01261.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-24138C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161343340 | ||||||
chr2:161343343
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.49-24135G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161343343 | ||||||
chr2:161343556
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.49-23922A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161343556 | ||||||
chr2:161343827
|
CAA | C | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.49-23637_49-23636d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161343827 | |||||
chr2:161343858
|
G | C | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49-23620G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161343858 | ||||||
chr2:161344047
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.49-23431A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344047 | ||||||
chr2:161344162
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.49-23316G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344162 | ||||||
chr2:161344180
|
A | G | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.49-23298A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344180 | ||||||
chr2:161344287
|
T | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 77 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.49-23191T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344287 | ||||||
chr2:161344554
|
G | A | 109 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.49-22924G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344554 | ||||||
chr2:161344565
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.49-22913C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344565 | ||||||
chr2:161344633
|
GTTC | G | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.49-22839_49-22837d others(5): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161344633 | |||||
chr2:161344650
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG02257.hp2 HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.49-22828A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344650 | ||||||
chr2:161344814
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.49-22664T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344814 | ||||||
chr2:161345148
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-22330G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161345148 | ||||||
chr2:161345170
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49-22308T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161345170 | ||||||
chr2:161345236
|
CT | C | 216 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(213): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.49-22218delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161345236 | |||||
chr2:161345435
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49-22043G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161345435 | ||||||
chr2:161345864
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.49-21614T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161345864 | ||||||
chr2:161345866
|
T | A | 1 | a0001c0001t0003g0097 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.49-21612T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161345866 | ||||||
chr2:161346117
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-21361C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161346117 | ||||||
chr2:161347191
|
G | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.49-20287G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161347191 | ||||||
chr2:161347264
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.49-20214T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161347264 | ||||||
chr2:161347385
|
C | T | 201 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.49-20093C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161347385 | ||||||
chr2:161347729
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49-19749C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161347729 | ||||||
chr2:161347844
|
CTT | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0028others(1): Show | 4 | HG03225.hp2 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-19632_49-19631d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161347844 | |||||
chr2:161347912
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.49-19566A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161347912 | ||||||
chr2:161348131
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.49-19347A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161348131 | ||||||
chr2:161348550
|
A | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-18928A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161348550 | ||||||
chr2:161348560
|
C | T | 2 | a0001c0001t0002g0060a0001c0001t0002g0114 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.49-18918C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161348560 | ||||||
chr2:161348927
|
ATTTG | A | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0217others(1): Show | 4 | HG02922.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-18548_49-18545d others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161348927 | |||||
chr2:161348932
|
T | C | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0217others(1): Show | 4 | HG02922.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-18546T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161348932 | ||||||
chr2:161349241
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49-18237G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161349241 | ||||||
chr2:161349882
|
A | G | 4 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01192.hp2 NA19004.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-17596A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161349882 | ||||||
chr2:161350294
|
A | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.49-17184A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161350294 | ||||||
chr2:161350735
|
C | G | 2 | a0001c0001t0002g0072a0001c0001t0002g0073 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.49-16743C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161350735 | ||||||
chr2:161350835
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-16643C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161350835 | ||||||
chr2:161350853
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.49-16625G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161350853 | ||||||
chr2:161350854
|
C | A | 1 | a0001c0001t0002g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.49-16624C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161350854 | ||||||
chr2:161350999
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(60): Show | 65 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.49-16479A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161350999 | ||||||
chr2:161351257
|
G | T | 2 | a0001c0001t0002g0163a0001c0001t0002g0167 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.49-16221G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351257 | ||||||
chr2:161351502
|
G | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.49-15976G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351502 | ||||||
chr2:161351747
|
C | T | 108 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(105): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.49-15731C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351747 | ||||||
chr2:161351848
|
A | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00544.hp1 HG02074.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.49-15630A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351848 | ||||||
chr2:161351849
|
T | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00544.hp1 HG02074.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.49-15629T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351849 | ||||||
chr2:161351850
|
T | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00544.hp1 HG02074.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.49-15628T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351850 | ||||||
chr2:161351912
|
G | C | 6 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(3): Show | 6 | HG02630.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-15566G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351912 | ||||||
chr2:161351933
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0051 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.49-15545G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351933 | ||||||
chr2:161352026
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.49-15452G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161352026 | ||||||
chr2:161352100
|
A | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA19004.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.49-15378A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161352100 | ||||||
chr2:161352199
|
A | G | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.49-15279A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161352199 | ||||||
chr2:161352474
|
G | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.49-15004G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161352474 | ||||||
chr2:161352693
|
C | T | 1 | a0001c0001t0004g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49-14785C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161352693 | ||||||
chr2:161352888
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49-14590C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161352888 | ||||||
chr2:161353089
|
C | A | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49-14389C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161353089 | ||||||
chr2:161353124
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.49-14354T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161353124 | ||||||
chr2:161353403
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.49-14075A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161353403 | ||||||
chr2:161353457
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49-14021A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161353457 | ||||||
chr2:161354120
|
C | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(56): Show | 61 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.49-13358C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161354120 | ||||||
chr2:161354129
|
T | G | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49-13349T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161354129 | ||||||
chr2:161354356
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.49-13122C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161354356 | ||||||
chr2:161354486
|
G | A | 1 | a0001c0001t0004g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49-12992G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161354486 | ||||||
chr2:161354508
|
C | CCTTA | 242 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(239): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.49-12967_49-12966i others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161354508 | |||||
chr2:161354758
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.49-12720G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161354758 | ||||||
chr2:161354785
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.49-12693T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161354785 | ||||||
chr2:161354872
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0051 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.49-12606G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161354872 | ||||||
chr2:161355219
|
G | A | 109 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.49-12259G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161355219 | ||||||
chr2:161355307
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0002g0167 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.49-12171A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161355307 | ||||||
chr2:161355532
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.49-11946C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161355532 | ||||||
chr2:161355716
|
A | G | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.49-11762A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161355716 | ||||||
chr2:161356046
|
A | ATG | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.49-11431_49-11430i others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161356046 | |||||
chr2:161356047
|
T | TG | 171 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(168): Show | 172 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.49-11431_49-11430i others(3): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161356047 | ||||||
chr2:161356301
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.49-11177A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161356301 | ||||||
chr2:161356340
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.49-11138A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161356340 | ||||||
chr2:161356634
|
C | A | 8 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(5): Show | 8 | HG02040.hp2 HG02080.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-10844C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161356634 | ||||||
chr2:161356655
|
A | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00544.hp1 HG02074.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.49-10823A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161356655 | ||||||
chr2:161356660
|
A | C | 12 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0238others(9): Show | 12 | HG00609.hp1 HG00673.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.49-10818A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161356660 | ||||||
chr2:161356762
|
CT | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0117others(12): Show | 17 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.49-10700delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161356762 | |||||
chr2:161356762
|
CTT | C | 235 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(232): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.49-10701_49-10700d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161356762 | |||||
chr2:161356762
|
CTTT | C | 6 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0227others(3): Show | 6 | HG03209.hp1 HG03471.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-10702_49-10700d others(5): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161356762 | |||||
chr2:161356791
|
A | C | 1 | a0001c0001t0002g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.49-10687A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161356791 | ||||||
chr2:161357076
|
C | CTTTT | 120 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(117): Show | 121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.49-10393_49-10390d others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTT | 7 | a0001c0001t0002g0064a0001c0001t0002g0079a0001c0001t0002g0164others(4): Show | 7 | HG02080.hp2 HG02280.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-10394_49-10390d others(7): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0118 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.49-10390_49-10389i others(20): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(12): Show |
25 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0120others(22): Show | 25 | HG00438.hp2 HG01515.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(21): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(13): Show |
9 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0132others(6): Show | 9 | HG02015.hp2 HG02080.hp1 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(22): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(14): Show |
10 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(23): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG00735.hp2 HG01123.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(24): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0258 | 2 | HG03209.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.49-10390_49-10389i others(27): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(19): Show |
5 | a0001c0001t0001g0227a0001c0001t0001g0232a0001c0001t0001g0246others(2): Show | 5 | HG02055.hp2 HG03471.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(28): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(20): Show |
25 | a0001c0001t0001g0008a0001c0001t0001g0196a0001c0001t0001g0212others(22): Show | 25 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(29): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(21): Show |
19 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0207others(16): Show | 20 | HG00438.hp1 HG01952.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(30): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(22): Show |
6 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0231others(3): Show | 6 | HG00673.hp1 HG01192.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(31): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(23): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0195a0001c0001t0001g0199others(4): Show | 8 | HG00140.hp2 HG02145.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-10390_49-10389i others(32): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(24): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.49-10390_49-10389i others(33): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-10390_49-10389i others(36): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0217 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.49-10390_49-10389i others(37): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357076
|
C | CTTTTTTT others(32): Show |
1 | a0001c0001t0001g0201 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.49-10390_49-10389i others(41): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357076 | |||||
chr2:161357165
|
G | GA | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(5): Show | 8 | HG02258.hp2 HG02886.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-10302dupA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357165 | |||||
chr2:161357205
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.49-10273A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161357205 | ||||||
chr2:161357562
|
G | T | 1 | a0001c0001t0002g0063 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.49-9916G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161357562 | ||||||
chr2:161357903
|
C | CT | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.49-9563dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161357903 | |||||
chr2:161357919
|
G | C | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.49-9559G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161357919 | ||||||
chr2:161358295
|
G | T | 1 | a0001c0001t0001g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.49-9183G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161358295 | ||||||
chr2:161358583
|
C | G | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0012others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.49-8895C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161358583 | ||||||
chr2:161358705
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.49-8773G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161358705 | ||||||
chr2:161358772
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0150others(1): Show | 4 | HG00438.hp2 NA18987.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-8706G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161358772 | ||||||
chr2:161358824
|
C | T | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG00741.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.49-8654C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161358824 | ||||||
chr2:161358953
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.49-8525G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161358953 | ||||||
chr2:161359002
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.49-8476C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359002 | ||||||
chr2:161359052
|
C | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-8426C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359052 | ||||||
chr2:161359163
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.49-8315G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359163 | ||||||
chr2:161359361
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG00423.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.49-8117A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359361 | ||||||
chr2:161359440
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49-8038C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359440 | ||||||
chr2:161359443
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.49-8035T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359443 | ||||||
chr2:161359798
|
C | T | 5 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0030others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-7680C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359798 | ||||||
chr2:161359901
|
C | T | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG02886.hp2 HG03139.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-7577C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161359901 | ||||||
chr2:161360019
|
A | G | 4 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(1): Show | 4 | HG02630.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-7459A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161360019 | ||||||
chr2:161360107
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 5 | NA18954.hp2 NA18979.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-7371A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161360107 | ||||||
chr2:161360191
|
A | AT | 161 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(158): Show | 162 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.49-7271dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161360191 | |||||
chr2:161360191
|
A | ATT | 5 | a0001c0001t0002g0015a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | NA18975.hp2 NA18992.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-7272_49-7271dup others(2): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161360191 | |||||
chr2:161360281
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.49-7197G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161360281 | ||||||
chr2:161360366
|
G | GT | 6 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0012others(3): Show | 6 | HG01109.hp1 HG01123.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-7097dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161360366 | |||||
chr2:161360366
|
GT | G | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(117): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.49-7097delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161360366 | |||||
chr2:161360778
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.49-6700C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161360778 | ||||||
chr2:161361199
|
G | C | 1 | a0001c0001t0002g0095 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.49-6279G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161361199 | ||||||
chr2:161361250
|
A | G | 1 | a0001c0001t0004g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49-6228A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161361250 | ||||||
chr2:161361406
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.49-6072A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161361406 | ||||||
chr2:161361458
|
A | AT | 170 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(167): Show | 171 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.49-6010dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161361458 | |||||
chr2:161361468
|
T | TTC | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.49-6010_49-6009ins others(2): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161361468 | ||||||
chr2:161361494
|
A | C | 1 | a0001c0001t0002g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.49-5984A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161361494 | ||||||
chr2:161361832
|
C | T | 28 | a0001c0001t0002g0001a0001c0001t0002g0018a0001c0001t0002g0023others(25): Show | 29 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.49-5646C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161361832 | ||||||
chr2:161362103
|
G | A | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.49-5375G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161362103 | ||||||
chr2:161362269
|
T | TA | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.49-5206dupA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161362269 | |||||
chr2:161362277
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49-5201A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161362277 | ||||||
chr2:161362739
|
A | G | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.49-4739A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161362739 | ||||||
chr2:161363106
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.49-4372G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161363106 | ||||||
chr2:161363227
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.49-4251C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161363227 | ||||||
chr2:161363288
|
T | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.49-4190T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161363288 | ||||||
chr2:161363409
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.49-4069A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161363409 | ||||||
chr2:161363574
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.49-3904T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161363574 | ||||||
chr2:161364042
|
G | C | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49-3436G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161364042 | ||||||
chr2:161364414
|
G | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0146others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.49-3064G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161364414 | ||||||
chr2:161364454
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.49-3024G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161364454 | ||||||
chr2:161364653
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0002g0167 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.49-2825A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161364653 | ||||||
chr2:161365183
|
G | A | 78 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0146others(75): Show | 78 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.49-2295G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161365183 | ||||||
chr2:161365468
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49-2010C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161365468 | ||||||
chr2:161365751
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.49-1727T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161365751 | ||||||
chr2:161366159
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.49-1319A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161366159 | ||||||
chr2:161366387
|
A | AAC | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.49-1057_49-1056dup others(2): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161366387 | |||||
chr2:161366387
|
AAC | A | 121 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0146others(118): Show | 122 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.49-1057_49-1056del others(2): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161366387 | |||||
chr2:161366387
|
AACAC | A | 13 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0225others(10): Show | 13 | HG00639.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.49-1059_49-1056del others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161366387 | |||||
chr2:161366387
|
AACACAC | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.49-1061_49-1056del others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 161366387 | |||||
chr2:161367682
|
G | GT | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.121-97dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 161367682 | |||||
chr2:161367746
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121-38G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 4/11 | chr2 | 161367746 | ||||||
chr2:161367778
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0004g0165 | 2 | HG02055.hp2 HG04115.hp2 |
splice_region_variant&intron_variant | LOW | c.121-6C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 4/11 | chr2 | 161367778 | ||||||
chr2:161367984
|
A | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.240+81A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161367984 | ||||||
chr2:161368076
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.240+173C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161368076 | ||||||
chr2:161368153
|
C | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.240+250C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161368153 | ||||||
chr2:161368158
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.240+255G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161368158 | ||||||
chr2:161368643
|
C | G | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG02886.hp2 HG03139.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+740C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161368643 | ||||||
chr2:161368658
|
A | G | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(204): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.240+755A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161368658 | ||||||
chr2:161368852
|
T | TA | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.240+954dupA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 161368852 | |||||
chr2:161368885
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0259 | 2 | NA18747.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.240+982C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161368885 | ||||||
chr2:161368933
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.240+1030A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161368933 | ||||||
chr2:161369097
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.241-1010G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161369097 | ||||||
chr2:161369127
|
T | C | 1 | a0001c0001t0002g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.241-980T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161369127 | ||||||
chr2:161369162
|
T | G | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.241-945T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161369162 | ||||||
chr2:161369804
|
G | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.241-303G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161369804 | ||||||
chr2:161369825
|
G | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.241-282G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161369825 | ||||||
chr2:161369912
|
C | T | 1 | a0001c0001t0004g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.241-195C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 5/11 | chr2 | 161369912 | ||||||
chr2:161370247
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 5 | NA18954.hp2 NA18979.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+70G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 6/11 | chr2 | 161370247 | ||||||
chr2:161370327
|
A | G | 182 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0117others(179): Show | 183 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.311+150A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 6/11 | chr2 | 161370327 | ||||||
chr2:161370449
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.311+272T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 6/11 | chr2 | 161370449 | ||||||
chr2:161370744
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.312-428A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 6/11 | chr2 | 161370744 | ||||||
chr2:161372472
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.462+1150A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161372472 | ||||||
chr2:161372550
|
G | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.462+1228G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161372550 | ||||||
chr2:161372630
|
CT | C | 4 | a0001c0001t0002g0164a0001c0001t0002g0166a0001c0001t0002g0169others(1): Show | 4 | HG02280.hp1 NA18522.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+1316delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 161372630 | |||||
chr2:161372688
|
CTTGA | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.462+1370_462+1373d others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 161372688 | |||||
chr2:161372975
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.462+1653A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161372975 | ||||||
chr2:161373002
|
A | G | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.462+1680A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161373002 | ||||||
chr2:161373021
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.462+1699T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161373021 | ||||||
chr2:161373830
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.462+2508C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161373830 | ||||||
chr2:161373968
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.462+2646A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161373968 | ||||||
chr2:161374009
|
T | G | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.462+2687T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374009 | ||||||
chr2:161374196
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.462+2874A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374196 | ||||||
chr2:161374323
|
A | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.462+3001A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374323 | ||||||
chr2:161374483
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0123others(1): Show | 4 | NA18984.hp2 NA19007.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+3161A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374483 | ||||||
chr2:161374604
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.462+3282C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374604 | ||||||
chr2:161374661
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.462+3339G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374661 | ||||||
chr2:161374835
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.462+3513C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374835 | ||||||
chr2:161374877
|
A | G | 1 | a0001c0001t0002g0092 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.462+3555A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374877 | ||||||
chr2:161374961
|
A | T | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | NA18950.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.462+3639A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161374961 | ||||||
chr2:161375574
|
T | C | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.462+4252T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161375574 | ||||||
chr2:161375639
|
A | G | 2 | a0001c0001t0002g0152a0001c0001t0002g0167 | 2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.462+4317A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161375639 | ||||||
chr2:161375948
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.462+4626C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161375948 | ||||||
chr2:161375951
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.462+4629G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161375951 | ||||||
chr2:161376061
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0197 | 2 | NA18943.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.462+4739G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161376061 | ||||||
chr2:161376106
|
C | CAT | 3 | a0001c0001t0002g0036a0001c0001t0002g0055a0001c0001t0002g0076 | 3 | HG02615.hp2 NA19077.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.462+4798_462+4799d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 161376106 | |||||
chr2:161376468
|
T | C | 3 | a0001c0001t0001g0227a0001c0001t0001g0258a0001c0001t0002g0152 | 3 | HG03209.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.462+5146T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161376468 | ||||||
chr2:161376511
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.462+5189A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161376511 | ||||||
chr2:161376597
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.462+5275C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161376597 | ||||||
chr2:161376670
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.462+5348G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161376670 | ||||||
chr2:161376986
|
G | A | 3 | a0001c0001t0001g0227a0001c0001t0001g0258a0001c0001t0002g0152 | 3 | HG03209.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.462+5664G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161376986 | ||||||
chr2:161377097
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.462+5775T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161377097 | ||||||
chr2:161377894
|
T | C | 1 | a0001c0001t0002g0100 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.462+6572T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161377894 | ||||||
chr2:161378097
|
A | G | 134 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0146others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.462+6775A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161378097 | ||||||
chr2:161378385
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.462+7063C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161378385 | ||||||
chr2:161378423
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.463-7041T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161378423 | ||||||
chr2:161378614
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.463-6850A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161378614 | ||||||
chr2:161379344
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.463-6120G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161379344 | ||||||
chr2:161379580
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463-5884C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161379580 | ||||||
chr2:161380029
|
G | A | 3 | a0001c0001t0001g0227a0001c0001t0001g0258a0001c0001t0002g0152 | 3 | HG03209.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.463-5435G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161380029 | ||||||
chr2:161380289
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.463-5175A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161380289 | ||||||
chr2:161380849
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.463-4615G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161380849 | ||||||
chr2:161381182
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.463-4282C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161381182 | ||||||
chr2:161381349
|
A | T | 1 | a0001c0001t0002g0073 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.463-4115A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161381349 | ||||||
chr2:161381491
|
T | A | 3 | a0001c0001t0001g0227a0001c0001t0001g0258a0001c0001t0002g0152 | 3 | HG03209.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.463-3973T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161381491 | ||||||
chr2:161382308
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.463-3156G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161382308 | ||||||
chr2:161382710
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.463-2754C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161382710 | ||||||
chr2:161383177
|
A | G | 1 | a0001c0001t0002g0101 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.463-2287A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161383177 | ||||||
chr2:161383474
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.463-1990A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161383474 | ||||||
chr2:161383718
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.463-1746T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161383718 | ||||||
chr2:161383743
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.463-1721T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161383743 | ||||||
chr2:161383896
|
T | A | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.463-1568T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161383896 | ||||||
chr2:161383969
|
CTT | C | 4 | a0001c0001t0002g0051a0001c0001t0002g0169a0001c0001t0002g0170others(1): Show | 4 | NA20300.hp1 NA20300.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.463-1490_463-1489d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 161383969 | |||||
chr2:161384087
|
G | A | 7 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0068others(4): Show | 7 | HG00609.hp2 HG00621.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.463-1377G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161384087 | ||||||
chr2:161384547
|
A | ACT | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.463-916_463-915dup others(2): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 161384547 | |||||
chr2:161384802
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.463-662A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161384802 | ||||||
chr2:161385335
|
T | C | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.463-129T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161385335 | ||||||
chr2:161385715
|
C | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.570+144C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161385715 | ||||||
chr2:161386165
|
T | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570+594T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161386165 | ||||||
chr2:161386376
|
T | C | 1 | a0001c0001t0002g0095 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.570+805T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161386376 | ||||||
chr2:161386925
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.570+1354C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161386925 | ||||||
chr2:161387182
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.570+1611T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161387182 | ||||||
chr2:161387209
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.570+1638C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161387209 | ||||||
chr2:161387664
|
A | G | 1 | a0001c0001t0002g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.570+2093A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161387664 | ||||||
chr2:161388427
|
T | A | 10 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(7): Show | 10 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-2677T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161388427 | ||||||
chr2:161388848
|
G | C | 1 | a0001c0001t0001g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.571-2256G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161388848 | ||||||
chr2:161388863
|
C | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0219 | 3 | HG02300.hp2 NA18959.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.571-2241C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161388863 | ||||||
chr2:161389321
|
C | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.571-1783C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389321 | ||||||
chr2:161389360
|
C | G | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.571-1744C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389360 | ||||||
chr2:161389398
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.571-1706C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389398 | ||||||
chr2:161389513
|
G | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.571-1591G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389513 | ||||||
chr2:161389788
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.571-1316A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389788 | ||||||
chr2:161389883
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.571-1221T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389883 | ||||||
chr2:161389886
|
GTTGTT | G | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0202others(2): Show | 5 | HG03139.hp1 HG03453.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-1215_571-1211d others(7): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389886 | |||||
chr2:161389889
|
G | GTTGTTGT others(6): Show |
1 | a0001c0001t0002g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(15): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(8): Show |
2 | a0001c0001t0001g0196a0001c0001t0001g0251 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(17): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(10): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG02040.hp2 NA19004.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(19): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(12): Show |
2 | a0001c0001t0001g0231a0001c0001t0002g0107 | 2 | HG01978.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(21): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(18): Show |
2 | a0001c0001t0001g0129a0001c0001t0002g0031 | 2 | HG03130.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(27): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(20): Show |
1 | a0001c0001t0001g0173 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.571-1213_571-1212i others(29): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(21): Show |
3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0205 | 3 | HG02145.hp1 NA18975.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(30): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(24): Show |
1 | a0001c0001t0002g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(33): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(25): Show |
1 | a0001c0001t0002g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.571-1213_571-1212i others(34): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(33): Show |
2 | a0001c0001t0002g0023a0001c0001t0002g0026 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(42): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(39): Show |
1 | a0001c0001t0002g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(48): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTGT others(41): Show |
1 | a0001c0001t0001g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.571-1213_571-1212i others(50): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(3): Show |
9 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0144others(6): Show | 10 | HG03209.hp2 NA18943.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(12): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(4): Show |
7 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0227others(4): Show | 7 | HG02257.hp1 HG03471.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(13): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(5): Show |
2 | a0001c0001t0001g0139a0001c0001t0002g0014 | 2 | HG01243.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(14): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(6): Show |
1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(15): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(7): Show |
11 | a0001c0001t0001g0141a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00280.hp1 HG01515.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(16): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(15): Show |
2 | a0001c0001t0002g0071a0001c0001t0002g0115 | 2 | HG00621.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(24): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(8): Show |
8 | a0001c0001t0001g0214a0001c0001t0001g0224a0001c0001t0001g0235others(5): Show | 8 | HG00673.hp1 HG03831.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(17): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(9): Show |
7 | a0001c0001t0001g0008a0001c0001t0001g0215a0001c0001t0001g0216others(4): Show | 7 | HG02300.hp2 HG02897.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(18): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(10): Show |
15 | a0001c0001t0001g0006a0001c0001t0001g0206a0001c0001t0001g0209others(12): Show | 16 | HG00423.hp1 HG00438.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(19): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(11): Show |
3 | a0001c0001t0001g0222a0001c0001t0001g0232a0001c0001t0001g0249 | 3 | HG02074.hp1 HG02622.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(20): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(12): Show |
3 | a0001c0001t0001g0195a0001c0001t0001g0250a0001c0001t0001g0256 | 3 | HG00140.hp2 HG04228.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(21): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(13): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0248 | 2 | HG00544.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(22): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(14): Show |
5 | a0001c0001t0001g0149a0001c0001t0001g0213a0001c0001t0002g0018others(2): Show | 5 | HG01243.hp1 HG03017.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(23): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(15): Show |
17 | a0001c0001t0001g0175a0001c0001t0001g0212a0001c0001t0002g0016others(14): Show | 17 | HG00609.hp2 HG01192.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(24): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(16): Show |
18 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0148others(15): Show | 18 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(25): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(17): Show |
13 | a0001c0001t0001g0146a0001c0001t0001g0258a0001c0001t0002g0001others(10): Show | 14 | HG00741.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(26): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(34): Show |
1 | a0001c0001t0002g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.571-1213_571-1212i others(43): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(18): Show |
4 | a0001c0001t0002g0079a0001c0001t0002g0085a0001c0001t0002g0100others(1): Show | 4 | HG02074.hp2 NA18950.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(27): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(34): Show |
2 | a0001c0001t0002g0153a0001c0001t0002g0159 | 2 | HG00639.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(43): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(35): Show |
5 | a0001c0001t0002g0154a0001c0001t0002g0156a0001c0001t0002g0160others(2): Show | 5 | HG01261.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(44): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(19): Show |
4 | a0001c0001t0002g0034a0001c0001t0002g0064a0001c0001t0002g0086others(1): Show | 4 | HG02080.hp2 HG03491.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(28): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(37): Show |
2 | a0001c0001t0002g0155a0001c0001t0002g0157 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(46): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(20): Show |
3 | a0001c0001t0001g0147a0001c0001t0002g0012a0001c0001t0002g0083 | 3 | HG00323.hp1 HG02056.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(29): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(21): Show |
2 | a0001c0001t0002g0035a0001c0001t0002g0098 | 2 | HG00673.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(30): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(22): Show |
3 | a0001c0001t0001g0142a0001c0001t0002g0013a0001c0001t0002g0074 | 3 | HG00423.hp2 HG02809.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(31): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(23): Show |
3 | a0001c0001t0001g0125a0001c0001t0002g0055a0001c0001t0002g0073 | 3 | HG01891.hp1 NA18959.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(32): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(24): Show |
4 | a0001c0001t0002g0033a0001c0001t0002g0095a0001c0001t0003g0039others(1): Show | 4 | HG01358.hp2 HG02004.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(33): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(25): Show |
5 | a0001c0001t0001g0126a0001c0001t0002g0015a0001c0001t0002g0053others(2): Show | 5 | HG02040.hp1 NA18948.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(34): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(27): Show |
3 | a0001c0001t0001g0174a0001c0001t0002g0027a0001c0001t0002g0089 | 3 | NA18987.hp1 NA19043.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(36): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(28): Show |
2 | a0001c0001t0001g0131a0001c0001t0002g0075 | 2 | HG03927.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(37): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(29): Show |
1 | a0001c0001t0002g0168 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(38): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(30): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0138a0001c0001t0001g0143others(1): Show | 4 | HG00438.hp2 HG01081.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1213_571-1212i others(39): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(31): Show |
1 | a0001c0001t0001g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.571-1213_571-1212i others(40): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(32): Show |
3 | a0001c0001t0001g0137a0001c0001t0002g0009a0001c0001t0002g0105 | 3 | HG01261.hp2 HG02135.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1212i others(41): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(34): Show |
1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(43): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(35): Show |
1 | a0001c0001t0002g0087 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(44): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(36): Show |
1 | a0001c0001t0001g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(45): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTGTTTT others(60): Show |
1 | a0001c0001t0001g0171 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.571-1213_571-1212i others(69): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.571-1206_571-1192d others(17): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0242 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.571-1207_571-1192d others(18): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(12): Show |
1 | a0001c0001t0001g0244 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.571-1210_571-1192d others(21): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(14): Show |
1 | a0001c0001t0002g0167 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1212_571-1192d others(23): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(15): Show |
2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | NA18939.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.571-1213_571-1192d others(24): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(16): Show |
1 | a0001c0001t0002g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.571-1214_571-1192d others(25): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0150 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.571-1192_571-1191i others(26): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389889
|
G | GTTTTTTT others(23): Show |
1 | a0001c0001t0002g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.571-1192_571-1191i others(32): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 161389889 | |||||
chr2:161389892
|
T | G | 4 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(1): Show | 4 | HG02630.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1212T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389892 | ||||||
chr2:161389910
|
T | G | 1 | a0001c0001t0002g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.571-1194T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389910 | ||||||
chr2:161389912
|
T | A | 16 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(13): Show | 16 | HG02145.hp2 HG02809.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.571-1192T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389912 | ||||||
chr2:161389912
|
T | TTTTTTTT others(25): Show |
1 | a0001c0001t0002g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.571-1192_571-1191i others(34): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389912 | ||||||
chr2:161389912
|
T | TTTTTTTT others(27): Show |
1 | a0001c0001t0002g0029 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.571-1192_571-1191i others(36): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389912 | ||||||
chr2:161389998
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0166 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.571-1106G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161389998 | ||||||
chr2:161390204
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.571-900A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161390204 | ||||||
chr2:161390329
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.571-775A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161390329 | ||||||
chr2:161390410
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.571-694G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161390410 | ||||||
chr2:161390491
|
G | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0073 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.571-613G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161390491 | ||||||
chr2:161390771
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.571-333A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161390771 | ||||||
chr2:161390888
|
A | G | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.571-216A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 8/11 | chr2 | 161390888 | ||||||
chr2:161391245
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.645+67G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161391245 | ||||||
chr2:161391261
|
C | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.645+83C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161391261 | ||||||
chr2:161391267
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.645+89T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161391267 | ||||||
chr2:161391630
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.645+452C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161391630 | ||||||
chr2:161391977
|
A | G | 3 | a0001c0001t0002g0024a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA20129.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.645+799A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161391977 | ||||||
chr2:161392040
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG02135.hp1 NA18943.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+862C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392040 | ||||||
chr2:161392080
|
T | G | 5 | a0001c0001t0002g0024a0001c0001t0002g0164a0001c0001t0002g0166others(2): Show | 5 | HG02280.hp1 NA18522.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.645+902T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392080 | ||||||
chr2:161392161
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.645+983A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392161 | ||||||
chr2:161392313
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.645+1135C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392313 | ||||||
chr2:161392317
|
G | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.645+1139G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392317 | ||||||
chr2:161392460
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.645+1282C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392460 | ||||||
chr2:161392509
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.645+1331G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392509 | ||||||
chr2:161392695
|
A | G | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.645+1517A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392695 | ||||||
chr2:161392937
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.645+1759T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161392937 | ||||||
chr2:161393815
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.646-1263C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161393815 | ||||||
chr2:161393816
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.646-1262G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161393816 | ||||||
chr2:161393821
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.646-1257A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161393821 | ||||||
chr2:161393848
|
A | G | 5 | a0001c0001t0002g0024a0001c0001t0002g0164a0001c0001t0002g0166others(2): Show | 5 | HG02280.hp1 NA18522.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1230A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161393848 | ||||||
chr2:161393971
|
A | AT | 172 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0118others(169): Show | 173 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.646-1085dupT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 161393971 | |||||
chr2:161393971
|
A | ATT | 12 | a0001c0001t0001g0119a0001c0001t0001g0139a0001c0001t0002g0017others(9): Show | 12 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.646-1086_646-1085d others(4): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 161393971 | |||||
chr2:161394031
|
C | T | 6 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0081others(3): Show | 6 | NA18950.hp2 NA18990.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1047C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394031 | ||||||
chr2:161394063
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.646-1015C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394063 | ||||||
chr2:161394081
|
T | G | 28 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(25): Show | 28 | HG00438.hp2 HG02040.hp2 HG02080.hp1 others(25): Show |
intron_variant | MODIFIER | c.646-997T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394081 | ||||||
chr2:161394325
|
A | G | 10 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(7): Show | 10 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-753A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394325 | ||||||
chr2:161394359
|
G | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0100a0001c0001t0002g0111 | 3 | NA19057.hp2 NA19060.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.646-719G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394359 | ||||||
chr2:161394399
|
C | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.646-679C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394399 | ||||||
chr2:161394786
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.646-292A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394786 | ||||||
chr2:161394926
|
T | C | 80 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0148others(77): Show | 80 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.646-152T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | chr2 | 161394926 | ||||||
chr2:161394988
|
GT | G | 6 | a0001c0001t0001g0125a0001c0001t0002g0060a0001c0001t0002g0061others(3): Show | 6 | HG02630.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-77delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 161394988 | |||||
chr2:161395345
|
C | G | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.771+142C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161395345 | ||||||
chr2:161395710
|
G | GA | 3 | a0001c0001t0001g0227a0001c0001t0001g0258a0001c0001t0002g0152 | 3 | HG03209.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.771+511dupA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 161395710 | |||||
chr2:161395910
|
A | G | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.771+707A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161395910 | ||||||
chr2:161396059
|
A | C | 3 | a0001c0001t0002g0152a0001c0001t0002g0163a0001c0001t0002g0167 | 3 | HG02280.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.771+856A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396059 | ||||||
chr2:161396108
|
G | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.771+905G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396108 | ||||||
chr2:161396227
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.771+1024G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396227 | ||||||
chr2:161396388
|
C | G | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.771+1185C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396388 | ||||||
chr2:161396598
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.771+1395G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396598 | ||||||
chr2:161396600
|
G | T | 1 | a0001c0001t0002g0022 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.771+1397G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396600 | ||||||
chr2:161396704
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.771+1501C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396704 | ||||||
chr2:161396924
|
T | C | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.771+1721T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396924 | ||||||
chr2:161396976
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.771+1773C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161396976 | ||||||
chr2:161397230
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.771+2027A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161397230 | ||||||
chr2:161397537
|
G | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0258a0001c0001t0002g0152 | 3 | HG03209.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.771+2334G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161397537 | ||||||
chr2:161397579
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.771+2376G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161397579 | ||||||
chr2:161397677
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.771+2474G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161397677 | ||||||
chr2:161397968
|
T | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG00438.hp2 NA18943.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.771+2765T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161397968 | ||||||
chr2:161398415
|
A | T | 12 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0238others(9): Show | 12 | HG00609.hp1 HG00673.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.771+3212A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161398415 | ||||||
chr2:161398555
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.771+3352A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161398555 | ||||||
chr2:161398663
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.771+3460C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161398663 | ||||||
chr2:161399267
|
C | T | 25 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(22): Show | 25 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.771+4064C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161399267 | ||||||
chr2:161399327
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.771+4124A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161399327 | ||||||
chr2:161399378
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.771+4175C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161399378 | ||||||
chr2:161399439
|
A | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.771+4236A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161399439 | ||||||
chr2:161399575
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.771+4372A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161399575 | ||||||
chr2:161399851
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.771+4648G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161399851 | ||||||
chr2:161399960
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(58): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.771+4757C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161399960 | ||||||
chr2:161400419
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.771+5216C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161400419 | ||||||
chr2:161400621
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0148others(3): Show | 6 | HG02015.hp2 HG02083.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+5418A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161400621 | ||||||
chr2:161400716
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.771+5513G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161400716 | ||||||
chr2:161400859
|
GA | G | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG02886.hp2 HG03139.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+5667delA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 161400859 | |||||
chr2:161400950
|
T | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.771+5747T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161400950 | ||||||
chr2:161400964
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.771+5761A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161400964 | ||||||
chr2:161401037
|
T | C | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.771+5834T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401037 | ||||||
chr2:161401288
|
T | A | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.771+6085T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401288 | ||||||
chr2:161401355
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.771+6152C>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401355 | ||||||
chr2:161401373
|
C | A | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.771+6170C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401373 | ||||||
chr2:161401423
|
G | T | 20 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(17): Show | 20 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.771+6220G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401423 | ||||||
chr2:161401539
|
G | A | 10 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(7): Show | 10 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.771+6336G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401539 | ||||||
chr2:161401684
|
A | G | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.771+6481A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401684 | ||||||
chr2:161401778
|
C | CATT | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(204): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.771+6591_771+6593d others(5): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 161401778 | |||||
chr2:161401922
|
C | T | 117 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0146others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.771+6719C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161401922 | ||||||
chr2:161402090
|
C | T | 6 | a0001c0001t0001g0136a0001c0001t0002g0037a0001c0001t0002g0038others(3): Show | 6 | HG00741.hp2 HG01192.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-6747C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402090 | ||||||
chr2:161402194
|
T | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.772-6643T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402194 | ||||||
chr2:161402217
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.772-6620T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402217 | ||||||
chr2:161402429
|
G | A | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.772-6408G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402429 | ||||||
chr2:161402575
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.772-6262A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402575 | ||||||
chr2:161402686
|
A | T | 1 | a0001c0001t0004g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.772-6151A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402686 | ||||||
chr2:161402698
|
GA | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.772-6128delA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 161402698 | |||||
chr2:161402758
|
A | T | 1 | a0001c0001t0002g0073 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.772-6079A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402758 | ||||||
chr2:161402911
|
G | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0146others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.772-5926G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161402911 | ||||||
chr2:161403202
|
TACTC | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0148others(3): Show | 6 | HG02015.hp2 HG02083.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-5633_772-5630d others(6): Show |
PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 161403202 | |||||
chr2:161403219
|
G | T | 1 | a0001c0001t0003g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.772-5618G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161403219 | ||||||
chr2:161403412
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.772-5425G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161403412 | ||||||
chr2:161403816
|
C | T | 28 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(25): Show | 28 | HG00438.hp2 HG02040.hp2 HG02080.hp1 others(25): Show |
intron_variant | MODIFIER | c.772-5021C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161403816 | ||||||
chr2:161403903
|
A | C | 1 | a0001c0001t0002g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.772-4934A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161403903 | ||||||
chr2:161403910
|
AT | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0150others(3): Show | 6 | HG00438.hp2 HG02451.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.772-4914delT | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 161403910 | |||||
chr2:161403965
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(58): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.772-4872A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161403965 | ||||||
chr2:161404392
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 5 | NA18954.hp2 NA18979.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-4445G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161404392 | ||||||
chr2:161404431
|
A | C | 3 | a0001c0001t0002g0024a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA20129.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.772-4406A>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161404431 | ||||||
chr2:161404536
|
G | T | 1 | a0001c0001t0002g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.772-4301G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161404536 | ||||||
chr2:161404629
|
G | A | 3 | a0001c0001t0001g0227a0001c0001t0001g0258a0001c0001t0002g0152 | 3 | HG03209.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.772-4208G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161404629 | ||||||
chr2:161404878
|
C | T | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(204): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.772-3959C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161404878 | ||||||
chr2:161404965
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.772-3872C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161404965 | ||||||
chr2:161405355
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.772-3482C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161405355 | ||||||
chr2:161405520
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.772-3317A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161405520 | ||||||
chr2:161405536
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.772-3301G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161405536 | ||||||
chr2:161405698
|
C | T | 1 | a0001c0001t0002g0022 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.772-3139C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161405698 | ||||||
chr2:161405758
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.772-3079C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161405758 | ||||||
chr2:161405831
|
C | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.772-3006C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161405831 | ||||||
chr2:161406154
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.772-2683G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161406154 | ||||||
chr2:161406637
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.772-2200A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161406637 | ||||||
chr2:161406850
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.772-1987A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161406850 | ||||||
chr2:161406964
|
T | G | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-1873T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161406964 | ||||||
chr2:161407250
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.772-1587A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161407250 | ||||||
chr2:161407279
|
G | T | 1 | a0001c0001t0002g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.772-1558G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161407279 | ||||||
chr2:161407333
|
A | T | 117 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0146others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.772-1504A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161407333 | ||||||
chr2:161407423
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.772-1414T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161407423 | ||||||
chr2:161407629
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0042 | 2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.772-1208T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161407629 | ||||||
chr2:161407704
|
G | A | 18 | a0001c0001t0001g0136a0001c0001t0002g0001a0001c0001t0002g0018others(15): Show | 19 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.772-1133G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161407704 | ||||||
chr2:161407766
|
T | C | 253 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.772-1071T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161407766 | ||||||
chr2:161408067
|
A | G | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0122others(3): Show | 6 | NA18961.hp1 NA18977.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.772-770A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161408067 | ||||||
chr2:161408481
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.772-356A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161408481 | ||||||
chr2:161408534
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.772-303C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161408534 | ||||||
chr2:161408678
|
G | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.772-159G>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161408678 | ||||||
chr2:161408759
|
A | G | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 77 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.772-78A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 10/11 | chr2 | 161408759 | ||||||
chr2:161409129
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG02145.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.834+230C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161409129 | ||||||
chr2:161409162
|
TA | T | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG03139.hp1 HG03453.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+265delA | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 161409162 | |||||
chr2:161409359
|
A | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.834+460A>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161409359 | ||||||
chr2:161409381
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0251 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.834+482A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161409381 | ||||||
chr2:161409828
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.834+929C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161409828 | ||||||
chr2:161410180
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0051 | 3 | HG02615.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.835-1122A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161410180 | ||||||
chr2:161410260
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.835-1042T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161410260 | ||||||
chr2:161410596
|
C | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0030 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.835-706C>T | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161410596 | ||||||
chr2:161410650
|
G | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.835-652G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161410650 | ||||||
chr2:161410708
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.835-594T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161410708 | ||||||
chr2:161410935
|
T | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.835-367T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161410935 | ||||||
chr2:161411111
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.835-191T>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161411111 | ||||||
chr2:161411202
|
G | C | 1 | a0001c0001t0002g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.835-100G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161411202 | ||||||
chr2:161411290
|
T | C | 3 | a0001c0001t0002g0024a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA20129.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.835-12T>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 11/11 | chr2 | 161411290 |