Item | Value |
---|---|
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 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 930 | 268 | 72 | 34 | 116 | 12 | 32 | PSMD14_chr2_161303425_161416717 | PSMD14 | ATGGA others(925): Show |
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 | AAGTG others(1562): Show |
chr2 | 161303425 | 161416717 |
a0001c0001t0002 | 0/1 | 1567 | 124 | 42 | 16 | 49 | 7 | 9 | PSMD14_chr2_161303425_161416717 | PSMD14 | AAGTG others(1562): Show |
chr2 | 161303425 | 161416717 |
a0001c0001t0003 | 0/0 | 1567 | 5 | 0 | 4 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | AAGTG others(1562): Show |
chr2 | 161303425 | 161416717 |
a0001c0001t0004 | 0/0 | 1567 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | AAGTG others(1562): Show |
chr2 | 161303425 | 161416717 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0182 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0097 | 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 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 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 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 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 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
a0001c0001t0004g0157 | 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 | g0048 | EUR | GBR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0084 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0050 | 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 | g0140 | 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 | g0024 | EUR | IBS | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0206 | 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 | g0087 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ASW | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ASW | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | TSI | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | USA | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0060 | REF | REF | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0184 | REF | REF | PSMD14_chr2_161303425_161416717 | PSMD14 | chr2 | 161303425 | 161416717 |
view | 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 |
---|
view | 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 |
---|
view | 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 | a0001c0001t0002 a0001c0001t0003 |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): 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 |
view | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
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 | 70 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(67): 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 | a0001c0001t0002g0017 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0019 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0003g0173 a0001c0001t0003g0174 |
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 | a0001c0001t0002g0172 | 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 | a0001c0001t0001g0016 | 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 | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): 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 | a0001c0001t0002g0020 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0171 | 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 | 11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): 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 | 166 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0116 others(163): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(173): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0109 | 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 others(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 | a0001c0001t0001g0015 | 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 | 62 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): 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 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
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 | a0001c0001t0002g0026 | 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 | 191 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(188): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): 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 | a0001c0001t0003g0174 | 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 | a0001c0001t0002g0108 | 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 | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(115): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): 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 | a0001c0001t0001g0188 a0001c0001t0001g0243 |
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 | a0001c0001t0001g0190 | 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 | a0001c0001t0002g0110 | 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0015 a0001c0001t0004g0157 |
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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(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 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(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 | 72 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(69): Show |
75 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(72): 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 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(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 | 221 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(218): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
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 | a0001c0001t0002g0039 a0001c0001t0002g0111 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
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 | a0001c0001t0002g0104 | 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 | 74 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): 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 | a0001c0001t0002g0151 | 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 | 191 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(188): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): 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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | |||||||
chr2:161319035 | CAT | C | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0055 | 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 | 182 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0116 others(179): Show |
192 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(189): 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 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(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 | a0001c0001t0002g0160 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.48+1306G>C | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161320179 | |||||||
chr2:161320973 | G | A | 1 | a0001c0001t0002g0160 | 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 | a0001c0001t0001g0132 | 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 | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(115): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0001t0002g0103 | 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 | a0001c0001t0001g0197 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0181 | 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 | 1 | a0001c0001t0002g0006 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0015 a0001c0001t0002g0102 a0001c0001t0002g0151 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
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 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | a0001c0001t0001g0181 | 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 | 62 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0002g0040 | 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 | a0001c0001t0002g0054 | 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 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0020 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0002g0041 | 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 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(115): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.48+8123T>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161326996 | |||||||
chr2:161327019 | T | A | 1 | a0001c0001t0002g0003 | 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 | a0001c0001t0001g0163 | 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 | 72 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.48+8937G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327810 | |||||||
chr2:161327878 | T | TA | 62 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.48+9012C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161327885 | |||||||
chr2:161327914 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 25 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0133 others(22): 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 |
40 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(37): 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 | a0001c0001t0001g0014 a0001c0001t0001g0140 a0001c0001t0001g0141 others(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 |
12 | a0001c0001t0001g0201 a0001c0001t0001g0217 a0001c0001t0001g0238 others(9): 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 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0032 others(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 |
25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(22): 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 |
16 | a0001c0001t0001g0196 a0001c0001t0002g0021 a0001c0001t0002g0028 others(13): Show |
16 | HG00323.hp1 HG00423.hp2 HG02040.hp1 others(13): 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 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0030 others(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 | a0001c0001t0001g0194 a0001c0001t0002g0022 a0001c0001t0002g0068 others(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 | a0001c0001t0002g0023 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0002g0062 a0001c0001t0002g0099 a0001c0001t0002g0100 others(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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0063 | 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 | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(3): 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 | 1 | a0001c0001t0002g0006 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0158 | 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 | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): 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 | a0001c0001t0001g0011 a0001c0001t0001g0185 a0001c0001t0001g0186 |
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 | a0001c0001t0002g0058 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0244 |
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 | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(3): 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 | a0001c0001t0001g0204 | 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 | 61 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(58): 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 | a0001c0001t0002g0047 | 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 | 174 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0116 others(171): Show |
184 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(181): 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 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
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 | 68 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(68): 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 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0156 a0001c0001t0002g0159 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0250 a0001c0001t0002g0105 |
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 | 16 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0026 others(13): 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
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 | a0001c0001t0002g0080 a0001c0001t0002g0096 a0001c0001t0002g0101 others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0094 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0002g0070 | 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 | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(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 | a0001c0001t0002g0172 | 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 | a0001c0001t0003g0098 | 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0002g0042 | 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 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0160 others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(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 | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(115): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): 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 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
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 | 117 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(114): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): 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 | a0001c0001t0002g0080 a0001c0001t0002g0096 a0001c0001t0002g0101 others(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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.48+17497A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161336370 | |||||||
chr2:161336398 | G | A | 242 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(239): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | 72 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): 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 | a0001c0001t0002g0087 a0001c0001t0002g0100 |
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 | a0001c0001t0001g0215 | 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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0150 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0017 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.48+19330C>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161338203 | |||||||
chr2:161338341 | GTT | G | 232 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(229): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(3): 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 | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): 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 | 134 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(131): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): 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 | a0001c0001t0001g0132 a0001c0001t0001g0145 a0001c0001t0002g0032 others(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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | 191 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(188): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0059 a0001c0001t0002g0073 a0001c0001t0002g0078 others(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 | a0001c0001t0002g0075 | 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 | a0001c0001t0002g0047 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0086 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0002g0051 a0001c0001t0002g0056 |
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 | a0001c0001t0001g0016 | 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 | 63 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(60): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0210 others(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 | a0001c0001t0002g0093 a0001c0001t0002g0158 |
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 | 70 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(67): 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | 191 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(188): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0228 | 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 | 117 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(114): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): 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 | a0001c0001t0002g0042 a0001c0001t0002g0051 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0001t0002g0156 a0001c0001t0002g0159 |
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 | a0001c0001t0002g0040 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(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 | 3 | a0001c0001t0002g0008 a0001c0001t0002g0153 a0001c0001t0002g0154 |
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 | 1 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0198 | 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 | 233 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(230): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): 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 | a0001c0001t0002g0047 | 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0002g0046 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.49-23298A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161344180 | |||||||
chr2:161344287 | T | C | 74 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): 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 | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): 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 | a0001c0001t0002g0087 | 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 | 117 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(114): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0177 | 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 | a0001c0001t0002g0064 | 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 | a0001c0001t0002g0155 | 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 | 205 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(202): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0003g0098 | 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 | a0001c0001t0002g0152 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0187 | 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 | 190 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(187): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0036 others(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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0065 a0001c0001t0002g0113 |
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 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0209 others(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 | a0001c0001t0002g0172 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0041 | 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 | a0001c0001t0002g0041 | 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 | 62 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): 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 | a0001c0001t0002g0156 a0001c0001t0002g0159 |
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 | 234 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(231): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.49-15976G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161351502 | |||||||
chr2:161351747 | C | T | 102 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(99): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
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 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0002g0051 a0001c0001t0002g0056 |
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 | a0001c0001t0002g0159 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | 234 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(231): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.49-15279A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161352199 | |||||||
chr2:161352474 | G | A | 234 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(231): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0015 | 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 | 58 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): 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 | a0001c0001t0002g0156 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0004g0157 | 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 | 231 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(228): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0002g0051 a0001c0001t0002g0056 |
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 | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): 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 | a0001c0001t0002g0156 a0001c0001t0002g0159 |
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 | a0001c0001t0001g0236 | 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 | 234 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(231): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.49-11762A>G | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 3/11 | chr2 | 161355716 | |||||||
chr2:161356046 | A | ATG | 73 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): 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 | 161 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(158): Show |
171 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(168): 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0002g0017 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0230 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0116 others(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 | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): 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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0219 others(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 | a0001c0001t0002g0158 | 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 | 110 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(107): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): 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 | a0001c0001t0002g0069 a0001c0001t0002g0080 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0219 a0001c0001t0001g0224 a0001c0001t0001g0238 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0188 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0190 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0223 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0187 a0001c0001t0001g0191 others(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 |
1 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0150 | 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 | a0001c0001t0002g0068 | 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 | 117 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(114): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0116 | 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 | 117 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(114): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0149 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0055 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0038 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(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 | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0245 |
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 | 154 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(151): Show |
161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): 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 | a0001c0001t0002g0023 a0001c0001t0002g0090 a0001c0001t0002g0091 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0002g0020 others(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 | 115 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(112): 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0167 | 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 | 160 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(157): Show |
170 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(167): 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 | 72 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): 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 | a0001c0001t0002g0079 | 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 | 26 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0026 others(23): 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | a0001c0001t0002g0021 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0002g0055 | 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 | a0001c0001t0002g0081 | 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 | a0001c0001t0002g0047 | 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 | 124 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0145 others(121): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0002g0156 a0001c0001t0002g0159 |
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 | 74 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0145 others(71): Show |
77 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(74): 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0002g0057 | 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 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
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 | 115 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0145 others(112): Show |
121 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(118): 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 | 9 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0217 others(6): 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 | 107 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(104): 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0156 | 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 | a0001c0001t0001g0015 a0001c0001t0004g0157 |
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 | 72 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | 196 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(193): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0249 |
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 | a0001c0001t0002g0062 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0002g0066 | 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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 198 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(195): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): 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 | a0001c0001t0004g0157 | 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 | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0245 |
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 | 172 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0116 others(169): Show |
182 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(179): 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 | a0001c0001t0002g0081 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0016 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0161 others(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 | 1 | a0001c0001t0002g0003 | 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 | a0001c0001t0002g0049 | 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | a0001c0001t0002g0084 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0002g0047 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0002g0113 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0002g0093 | 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 | 1 | a0001c0001t0002g0006 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0159 |
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 | a0001c0001t0002g0064 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0189 |
2 | NA18943.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.462+4739G>A | PSMD14 | ENSG00000115233.12 | transcript | ENST00000409682.8 | protein_coding | 7/11 | chr2 | 161376061 | |||||||
chr2:161376468 | T | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0144 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0219 | 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 | a0001c0001t0002g0101 | 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 | 124 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0145 others(121): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): 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 | a0001c0001t0002g0154 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0002g0159 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0002g0151 |
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 | a0001c0001t0002g0029 | 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 | a0001c0001t0002g0057 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0190 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0056 a0001c0001t0002g0161 a0001c0001t0002g0162 others(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 | 6 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0074 others(3): 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | 63 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(60): 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0002g0109 | 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 | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(3): 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0164 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0194 others(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 | a0001c0001t0002g0038 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0243 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0223 a0001c0001t0002g0106 |
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 | a0001c0001t0001g0128 a0001c0001t0002g0039 |
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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0197 |
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 | a0001c0001t0002g0040 | 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 | a0001c0001t0002g0033 | 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 | a0001c0001t0002g0031 a0001c0001t0002g0034 |
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 | a0001c0001t0002g0111 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0138 a0001c0001t0002g0022 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0202 a0001c0001t0001g0203 others(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 | a0001c0001t0002g0074 a0001c0001t0002g0114 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0216 a0001c0001t0001g0227 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0207 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0198 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0224 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0242 a0001c0001t0001g0246 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0240 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0002g0026 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0204 a0001c0001t0002g0001 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0248 a0001c0001t0002g0001 others(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 | a0001c0001t0002g0152 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0080 a0001c0001t0002g0086 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0069 a0001c0001t0002g0087 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0007 |
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 | a0001c0001t0001g0146 a0001c0001t0002g0020 a0001c0001t0002g0084 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0099 |
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 | a0001c0001t0001g0141 a0001c0001t0002g0021 a0001c0001t0002g0077 |
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 |
2 | a0001c0001t0001g0125 a0001c0001t0002g0076 |
2 | HG01891.hp1 NA18959.hp2 |
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 | a0001c0001t0002g0041 a0001c0001t0002g0096 a0001c0001t0003g0044 others(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 | a0001c0001t0001g0124 a0001c0001t0002g0023 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0166 a0001c0001t0002g0035 a0001c0001t0002g0090 |
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 | a0001c0001t0001g0130 a0001c0001t0002g0005 |
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 | a0001c0001t0002g0160 | 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 | a0001c0001t0001g0118 a0001c0001t0001g0136 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0017 a0001c0001t0002g0104 |
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 | a0001c0001t0001g0137 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0002g0159 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0071 |
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 | a0001c0001t0002g0156 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0002g0158 | 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0001c0001t0002g0036 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0002g0155 a0001c0001t0002g0158 |
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 | a0001c0001t0002g0034 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0002g0070 | 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 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
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 | a0001c0001t0002g0155 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0064 | 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 | 198 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(195): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): 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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0032 a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0002g0032 a0001c0001t0002g0155 a0001c0001t0002g0158 others(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 | a0001c0001t0002g0084 | 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 | a0001c0001t0002g0024 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0002g0032 a0001c0001t0002g0155 a0001c0001t0002g0158 others(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 | 162 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(159): Show |
172 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(169): 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 | a0001c0001t0001g0123 a0001c0001t0001g0138 a0001c0001t0002g0025 others(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 | 4 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0082 others(1): 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(3): 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 | a0001c0001t0002g0080 a0001c0001t0002g0101 a0001c0001t0002g0110 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0187 | 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 | 76 | a0001c0001t0001g0018 a0001c0001t0001g0145 a0001c0001t0001g0147 others(73): Show |
79 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(76): 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 | a0001c0001t0001g0125 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0156 a0001c0001t0002g0159 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0052 | 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 | a0001c0001t0002g0030 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0168 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0002g0151 |
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 | a0001c0001t0002g0101 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0230 others(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 | a0001c0001t0002g0049 | 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 | a0001c0001t0002g0081 | 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 | 22 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0017 others(19): Show |
24 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(21): 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0002g0103 | 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 | 72 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0203 | 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 | 60 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0145 a0001c0001t0001g0147 others(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 | a0001c0001t0002g0161 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 198 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(195): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0055 | 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 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(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 | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(3): 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 196 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(193): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): 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 | 111 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0145 others(108): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): 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 | a0001c0001t0001g0134 a0001c0001t0002g0043 a0001c0001t0002g0045 others(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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0002g0021 | 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 | 198 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(195): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0004g0157 | 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 | 248 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(245): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): 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 | a0001c0001t0002g0076 | 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 | 124 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0145 others(121): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): 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 | a0001c0001t0001g0018 a0001c0001t0001g0145 a0001c0001t0001g0147 others(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 | a0001c0001t0003g0174 | 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 | a0001c0001t0003g0173 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0079 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0149 others(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 | 60 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): 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 | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0245 |
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 | a0001c0001t0002g0032 a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | a0001c0001t0002g0085 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0002g0151 |
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 | 197 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(194): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0002g0021 | 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 | a0001c0001t0002g0030 | 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 | a0001c0001t0002g0047 | 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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0002g0021 | 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 | a0001c0001t0002g0105 | 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 | 111 | a0001c0001t0001g0018 a0001c0001t0001g0134 a0001c0001t0001g0145 others(108): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0002g0026 a0001c0001t0002g0048 |
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 | 16 | a0001c0001t0001g0134 a0001c0001t0002g0001 a0001c0001t0002g0003 others(13): 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 | 242 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(239): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): 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 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | 74 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): 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 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): 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 | a0001c0001t0001g0188 a0001c0001t0001g0243 |
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 | a0001c0001t0002g0172 | 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 | a0001c0001t0002g0042 a0001c0001t0002g0051 a0001c0001t0002g0056 |
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 | a0001c0001t0002g0092 | 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 | a0001c0001t0002g0031 a0001c0001t0002g0038 |
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 | 249 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): 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 | a0001c0001t0001g0119 | 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 | 72 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0002g0032 a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 |