Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5707 |
| ensemblid | ENSG00000173692.14 |
| hgncid | 9554 |
| symbol | PSMD1 |
| name | proteasome 26S subunit, non-ATPase 1 |
| refseq_nuc | NM_002807.4 |
| refseq_prot | NP_002798.2 |
| ensembl_nuc | ENST00000308696.11 |
| ensembl_prot | ENSP00000309474.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 231056867 |
| end | 231172827 |
| strand | + |
| ver | v1.2 |
| region | chr2:231056867-231172827 |
| region5000 | chr2:231051867-231177827 |
| regionname0 | PSMD1_chr2_231056867_231172827 |
| regionname5000 | PSMD1_chr2_231051867_231177827 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 953 | 360 | 85 | 48 | 179 | 10 | 36 | 144 | PSMD1_chr2_231051867_231177827 | PSMD1 | MITSA others(948): Show |
chr2 | 231051867 | 231177827 |
| a0002 | 0/0 | 953 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | MITSA others(948): Show |
chr2 | 231051867 | 231177827 |
| a0003 | 0/0 | 953 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | MITSA others(948): Show |
chr2 | 231051867 | 231177827 |
| a0004 | 0/0 | 953 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | MITSA others(948): Show |
chr2 | 231051867 | 231177827 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2859 | 353 | 78 | 48 | 179 | 10 | 36 | PSMD1_chr2_231051867_231177827 | PSMD1 | ATGAT others(2854): Show |
chr2 | 231051867 | 231177827 | ||
| a0001c0002 | 0/0 | 2859 | 5 | 5 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | ATGAT others(2854): Show |
chr2 | 231051867 | 231177827 | ||
| a0001c0005 | 0/0 | 2859 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | ATGAT others(2854): Show |
chr2 | 231051867 | 231177827 | ||
| a0001c0006 | 0/0 | 2859 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | ATGAT others(2854): Show |
chr2 | 231051867 | 231177827 | ||
| a0002c0003 | 0/0 | 2859 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | ATGAT others(2854): Show |
chr2 | 231051867 | 231177827 | ||
| a0003c0007 | 0/0 | 2859 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | ATGAT others(2854): Show |
chr2 | 231051867 | 231177827 | ||
| a0004c0004 | 0/0 | 2859 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | ATGAT others(2854): Show |
chr2 | 231051867 | 231177827 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3323 | 192 | 42 | 22 | 111 | 2 | 15 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0001t0002 | 1/1 | 3323 | 101 | 8 | 21 | 51 | 4 | 15 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0001t0003 | 0/0 | 3323 | 57 | 27 | 5 | 16 | 4 | 5 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0001t0005 | 0/0 | 3323 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0001t0006 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0001t0007 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0002t0004 | 0/0 | 3323 | 5 | 5 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0005t0001 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0001c0006t0002 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0002c0003t0002 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0002c0003t0003 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0003c0007t0001 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| a0004c0004t0002 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | GTCCT others(3318): Show |
chr2 | 231051867 | 231177827 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0115 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0001c0006t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0002c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0003c0007t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| a0004c0004t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0145 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0344 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0162 | EUR | FIN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0160 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0146 | EUR | IBS | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01891 | hp1 | a0003 | c0007 | t0001 | g0239 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0156 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CDX | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0026 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02280 | hp2 | a0001 | c0006 | t0002 | g0105 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | KHV | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0351 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0279 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0335 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0121 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0030 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0350 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | BEB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | STU | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19003 | hp1 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19088 | hp1 | a0002 | c0003 | t0002 | g0081 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | YRI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0352 | AFR | ASW | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | TSI | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | GIH | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20300 | hp1 | a0001 | c0005 | t0001 | g0031 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | USA | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0116 | REF | REF | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0115 | REF | REF | PSMD1_chr2_231051867_231177827 | PSMD1 | chr2 | 231051867 | 231177827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:231067085 | G | A | 1 | a0002 | 2 | HG02129.hp1 NA19088.hp1 |
missense_variant | MODERATE | c.484G>A | p.Val162Ile | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/25 | 643/3323 | 484/2862 | 162/953 | chr2 | 231067085 | |||
| chr2:231067092 | A | C | 1 | a0003 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.491A>C | p.Glu164Ala | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/25 | 650/3323 | 491/2862 | 164/953 | chr2 | 231067092 | |||
| chr2:231153639 | A | G | 1 | a0004 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.2191A>G | p.Ile731Val | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/25 | 2350/3323 | 2191/2862 | 731/953 | chr2 | 231153639 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:231070117 | A | G | 1 | a0001c0006 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.603A>G | p.Leu201Leu | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/25 | 762/3323 | 603/2862 | 201/953 | chr2 | 231070117 | |||
| chr2:231072269 | A | G | 1 | a0001c0005 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.735A>G | p.Ala245Ala | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/25 | 894/3323 | 735/2862 | 245/953 | chr2 | 231072269 | |||
| chr2:231163682 | A | G | 1 | a0001c0002 | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.2436A>G | p.Ala812Ala | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/25 | 2595/3323 | 2436/2862 | 812/953 | chr2 | 231163682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:231056872 | G | C | 3 | a0001c0001t0003 a0001c0001t0005 a0002c0003t0003 |
59 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-154G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/25 | 154 | chr2 | 231056872 | ||||||
| chr2:231056930 | C | A | 1 | a0001c0001t0006 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/25 | 96 | chr2 | 231056930 | ||||||
| chr2:231056955 | C | G | 1 | a0001c0002t0004 | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-71C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/25 | 71 | chr2 | 231056955 | ||||||
| chr2:231170715 | G | A | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(5): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/25 | 3 | chr2 | 231170715 | ||||||
| chr2:231172709 | C | G | 1 | a0001c0001t0005 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 25/25 | 1997 | chr2 | 231172709 | ||||||
| chr2:231172803 | C | T | 1 | a0001c0001t0007 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 25/25 | 2091 | chr2 | 231172803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:231057179 | C | T | 2 | a0001c0001t0003g0351 a0001c0001t0003g0352 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.16+138C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057179 | |||||||
| chr2:231057232 | G | C | 12 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(9): Show |
12 | HG01346.hp2 HG03654.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.16+191G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057232 | |||||||
| chr2:231057236 | A | G | 1 | a0001c0001t0002g0350 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16+195A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057236 | |||||||
| chr2:231057272 | A | G | 1 | a0001c0001t0002g0349 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.16+231A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057272 | |||||||
| chr2:231057548 | A | G | 5 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+507A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057548 | |||||||
| chr2:231057654 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.16+613C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231057654 | |||||||
| chr2:231058123 | A | G | 1 | a0001c0001t0002g0342 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.16+1082A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058123 | |||||||
| chr2:231058285 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16+1244T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058285 | |||||||
| chr2:231058339 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.16+1298C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058339 | |||||||
| chr2:231058520 | CT | C | 57 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(54): Show |
59 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.16+1494delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231058520 | ||||||
| chr2:231058626 | C | T | 4 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0167 others(1): Show |
4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+1585C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058626 | |||||||
| chr2:231058716 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.16+1675T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058716 | |||||||
| chr2:231058825 | C | T | 2 | a0001c0001t0001g0340 a0001c0001t0003g0341 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.16+1784C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058825 | |||||||
| chr2:231058845 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.16+1804T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058845 | |||||||
| chr2:231058912 | A | C | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.16+1871A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231058912 | |||||||
| chr2:231058952 | G | GTC | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(48): Show |
53 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.16+1927_16+1928dup others(2): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231058952 | ||||||
| chr2:231059025 | A | G | 32 | a0001c0001t0003g0005 a0001c0001t0003g0134 a0001c0001t0003g0135 others(29): Show |
33 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.16+1984A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059025 | |||||||
| chr2:231059220 | T | C | 1 | a0001c0002t0004g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.17-2047T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059220 | |||||||
| chr2:231059223 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.17-2044A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059223 | |||||||
| chr2:231059235 | G | T | 1 | a0001c0001t0001g0338 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.17-2032G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059235 | |||||||
| chr2:231059493 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0211 a0001c0001t0001g0212 others(15): Show |
19 | HG02683.hp2 HG03490.hp2 HG03491.hp1 others(16): Show |
intron_variant | MODIFIER | c.17-1774G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059493 | |||||||
| chr2:231059501 | G | A | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.17-1766G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059501 | |||||||
| chr2:231059574 | A | C | 1 | a0001c0001t0001g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.17-1693A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059574 | |||||||
| chr2:231059651 | C | T | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17-1616C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231059651 | |||||||
| chr2:231060153 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.17-1114G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060153 | |||||||
| chr2:231060326 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.17-941A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060326 | |||||||
| chr2:231060450 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.17-817C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060450 | |||||||
| chr2:231060933 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.17-334C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060933 | |||||||
| chr2:231060952 | T | A | 1 | a0001c0001t0003g0136 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.17-315T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231060952 | |||||||
| chr2:231061035 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.17-232T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061035 | |||||||
| chr2:231061162 | C | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.17-105C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061162 | |||||||
| chr2:231061175 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.17-92G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061175 | |||||||
| chr2:231061218 | C | T | 4 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0003g0334 others(1): Show |
4 | HG02145.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-49C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 1/24 | chr2 | 231061218 | |||||||
| chr2:231061606 | C | G | 1 | a0001c0001t0002g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.60+296C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061606 | |||||||
| chr2:231061869 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.61-379G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061869 | |||||||
| chr2:231061877 | C | T | 1 | a0001c0001t0002g0350 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61-371C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061877 | |||||||
| chr2:231061896 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.61-352A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061896 | |||||||
| chr2:231061978 | G | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.61-270G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231061978 | |||||||
| chr2:231062106 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61-142T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231062106 | |||||||
| chr2:231062235 | T | C | 6 | a0001c0001t0003g0005 a0001c0001t0003g0137 a0001c0001t0003g0138 others(3): Show |
7 | HG03834.hp2 NA18963.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-13T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 2/24 | chr2 | 231062235 | |||||||
| chr2:231062690 | T | A | 2 | a0001c0001t0001g0340 a0001c0001t0003g0341 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.304+15T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062690 | |||||||
| chr2:231062855 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.304+180G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062855 | |||||||
| chr2:231062856 | G | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.304+181G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062856 | |||||||
| chr2:231062951 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.304+276G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231062951 | |||||||
| chr2:231063067 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.304+392A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063067 | |||||||
| chr2:231063178 | T | C | 2 | a0001c0001t0003g0118 a0001c0001t0003g0119 |
2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.304+503T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063178 | |||||||
| chr2:231063191 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0002g0035 |
2 | HG02258.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.304+516G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063191 | |||||||
| chr2:231063343 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.304+668G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063343 | |||||||
| chr2:231063396 | T | C | 1 | a0001c0001t0002g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.304+721T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063396 | |||||||
| chr2:231063497 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.304+822G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063497 | |||||||
| chr2:231063561 | T | A | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.304+886T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063561 | |||||||
| chr2:231063594 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.304+919G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231063594 | |||||||
| chr2:231063828 | AT | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
359 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.304+1166delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231063828 | ||||||
| chr2:231064261 | T | A | 1 | a0001c0001t0001g0290 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.304+1586T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064261 | |||||||
| chr2:231064302 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+1627A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064302 | |||||||
| chr2:231064324 | C | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304+1649C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064324 | |||||||
| chr2:231064463 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.304+1788A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064463 | |||||||
| chr2:231064916 | CT | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.305-1988delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231064916 | ||||||
| chr2:231064947 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0336 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.305-1959C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231064947 | |||||||
| chr2:231065002 | A | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG03927.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.305-1904A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065002 | |||||||
| chr2:231065052 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.305-1854C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065052 | |||||||
| chr2:231065063 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.305-1843A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065063 | |||||||
| chr2:231065177 | A | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.305-1729A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065177 | |||||||
| chr2:231065226 | A | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1680A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065226 | |||||||
| chr2:231065261 | G | GTTTTTTG others(1): Show |
5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1630_305-1623d others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065261 | ||||||
| chr2:231065261 | G | GTTTTTTG others(10): Show |
1 | a0001c0001t0003g0163 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.305-1622_305-1606d others(19): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065261 | ||||||
| chr2:231065354 | G | A | 6 | a0001c0001t0001g0025 a0001c0002t0004g0026 a0001c0002t0004g0027 others(3): Show |
6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-1552G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065354 | |||||||
| chr2:231065421 | T | A | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0118 others(53): Show |
58 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.305-1485T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065421 | |||||||
| chr2:231065459 | A | ATT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0004g0026 others(4): Show |
7 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.305-1435_305-1434d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065459 | ||||||
| chr2:231065459 | A | ATTT | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.305-1436_305-1434d others(5): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065459 | ||||||
| chr2:231065459 | A | ATTTT | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.305-1437_305-1434d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr2 | 231065459 | ||||||
| chr2:231065497 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.305-1409C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065497 | |||||||
| chr2:231065501 | G | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.305-1405G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065501 | |||||||
| chr2:231065591 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.305-1315G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065591 | |||||||
| chr2:231065835 | C | T | 11 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(8): Show |
11 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.305-1071C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065835 | |||||||
| chr2:231065852 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.305-1054G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065852 | |||||||
| chr2:231065968 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.305-938C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231065968 | |||||||
| chr2:231066206 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.305-700A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066206 | |||||||
| chr2:231066419 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.305-487T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066419 | |||||||
| chr2:231066502 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
252 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.305-404G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066502 | |||||||
| chr2:231066609 | G | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.305-297G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066609 | |||||||
| chr2:231066638 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0331 a0001c0001t0001g0332 others(1): Show |
5 | HG00438.hp1 HG00558.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-268C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066638 | |||||||
| chr2:231066657 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.305-249G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066657 | |||||||
| chr2:231066668 | C | T | 2 | a0001c0001t0003g0165 a0001c0001t0003g0168 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.305-238C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 4/24 | chr2 | 231066668 | |||||||
| chr2:231067349 | T | C | 9 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(6): Show |
9 | NA18948.hp1 NA18960.hp1 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+238T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067349 | |||||||
| chr2:231067420 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.510+309T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067420 | |||||||
| chr2:231067533 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510+422A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067533 | |||||||
| chr2:231067657 | T | C | 4 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+546T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067657 | |||||||
| chr2:231067802 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.510+691G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067802 | |||||||
| chr2:231067846 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.510+735G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231067846 | |||||||
| chr2:231068201 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510+1090A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068201 | |||||||
| chr2:231068372 | C | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.510+1261C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068372 | |||||||
| chr2:231068373 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+1262G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068373 | |||||||
| chr2:231068547 | A | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.510+1436A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068547 | |||||||
| chr2:231068686 | A | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.511-1339A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068686 | |||||||
| chr2:231068694 | C | T | 2 | a0001c0001t0002g0110 a0001c0001t0002g0117 |
2 | HG01081.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.511-1331C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068694 | |||||||
| chr2:231068944 | A | G | 7 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-1081A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231068944 | |||||||
| chr2:231069089 | C | A | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.511-936C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069089 | |||||||
| chr2:231069188 | T | A | 1 | a0001c0001t0002g0042 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.511-837T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069188 | |||||||
| chr2:231069188 | T | TA | 7 | a0001c0001t0001g0233 a0001c0001t0001g0285 a0001c0001t0001g0292 others(4): Show |
7 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-825dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231069188 | ||||||
| chr2:231069189 | A | T | 5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0286 others(2): Show |
5 | HG02155.hp1 NA18964.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-836A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069189 | |||||||
| chr2:231069998 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.511-27G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 5/24 | chr2 | 231069998 | |||||||
| chr2:231070215 | G | A | 3 | a0001c0002t0004g0027 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.654+47G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070215 | |||||||
| chr2:231070245 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.654+77A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070245 | |||||||
| chr2:231070252 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.654+84A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070252 | |||||||
| chr2:231070277 | A | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG01243.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.654+109A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070277 | |||||||
| chr2:231070484 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.654+316A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070484 | |||||||
| chr2:231070495 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0001g0327 others(3): Show |
7 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+327A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070495 | |||||||
| chr2:231070527 | A | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.654+359A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070527 | |||||||
| chr2:231070562 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.654+394C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070562 | |||||||
| chr2:231070611 | T | G | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.654+443T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070611 | |||||||
| chr2:231070885 | G | C | 4 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(1): Show |
4 | HG02027.hp1 NA18947.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+717G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070885 | |||||||
| chr2:231070962 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | HG00408.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.654+794C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231070962 | |||||||
| chr2:231071093 | G | T | 1 | a0001c0001t0003g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.654+925G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071093 | |||||||
| chr2:231071104 | C | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | NA18966.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.654+936C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071104 | |||||||
| chr2:231071204 | C | T | 39 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0122 others(36): Show |
41 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.655-985C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071204 | |||||||
| chr2:231071325 | G | A | 11 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(8): Show |
11 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.655-864G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071325 | |||||||
| chr2:231071615 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.655-574A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071615 | |||||||
| chr2:231071655 | A | T | 1 | a0001c0001t0002g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.655-534A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071655 | |||||||
| chr2:231071660 | G | A | 4 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-529G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071660 | |||||||
| chr2:231071770 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655-419T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071770 | |||||||
| chr2:231071917 | C | A | 3 | a0001c0002t0004g0027 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.655-272C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 6/24 | chr2 | 231071917 | |||||||
| chr2:231072536 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.881+121T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072536 | |||||||
| chr2:231072605 | T | C | 1 | a0001c0001t0002g0049 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.881+190T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072605 | |||||||
| chr2:231072791 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.881+376A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072791 | |||||||
| chr2:231072825 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.881+410T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072825 | |||||||
| chr2:231072893 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG00733.hp2 HG01081.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.881+478C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072893 | |||||||
| chr2:231072899 | G | A | 3 | a0001c0002t0004g0027 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.881+484G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231072899 | |||||||
| chr2:231073257 | A | G | 1 | a0001c0001t0003g0161 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.881+842A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073257 | |||||||
| chr2:231073292 | A | T | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.881+877A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073292 | |||||||
| chr2:231073332 | A | G | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 |
3 | NA18952.hp1 NA18957.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.881+917A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073332 | |||||||
| chr2:231073479 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0194 others(79): Show |
84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.881+1064C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073479 | |||||||
| chr2:231073507 | T | C | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+1092T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073507 | |||||||
| chr2:231073558 | G | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+1143G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073558 | |||||||
| chr2:231073588 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.881+1173G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073588 | |||||||
| chr2:231073621 | G | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.881+1206G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073621 | |||||||
| chr2:231073801 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.881+1386G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073801 | |||||||
| chr2:231073996 | C | A | 1 | a0001c0001t0003g0164 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882-1515C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231073996 | |||||||
| chr2:231074103 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.882-1408G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074103 | |||||||
| chr2:231074294 | C | T | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0006g0279 |
3 | HG02451.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.882-1217C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074294 | |||||||
| chr2:231074431 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882-1080G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074431 | |||||||
| chr2:231074700 | T | C | 4 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0167 others(1): Show |
4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-811T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074700 | |||||||
| chr2:231074798 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882-713A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074798 | |||||||
| chr2:231074812 | A | G | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.882-699A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074812 | |||||||
| chr2:231074917 | C | T | 3 | a0001c0002t0004g0027 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.882-594C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231074917 | |||||||
| chr2:231075253 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.882-258A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231075253 | |||||||
| chr2:231075339 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.882-172A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231075339 | |||||||
| chr2:231075408 | CATT | C | 3 | a0001c0001t0001g0282 a0001c0002t0004g0026 a0001c0002t0004g0030 |
3 | HG02280.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882-99_882-97delAT others(1): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr2 | 231075408 | ||||||
| chr2:231075425 | A | G | 3 | a0001c0002t0004g0027 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.882-86A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 7/24 | chr2 | 231075425 | |||||||
| chr2:231075648 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0194 others(79): Show |
84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.942+77C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075648 | |||||||
| chr2:231075740 | C | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | NA18968.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.942+169C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075740 | |||||||
| chr2:231075789 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.942+218C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075789 | |||||||
| chr2:231075872 | C | T | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.942+301C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075872 | |||||||
| chr2:231075878 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.942+307A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075878 | |||||||
| chr2:231075895 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.942+324G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075895 | |||||||
| chr2:231075930 | A | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.942+359A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075930 | |||||||
| chr2:231075950 | G | A | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.942+379G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075950 | |||||||
| chr2:231075957 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.942+386C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231075957 | |||||||
| chr2:231076149 | A | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.942+578A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076149 | |||||||
| chr2:231076162 | A | G | 12 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(9): Show |
12 | HG00408.hp2 HG02015.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.942+591A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076162 | |||||||
| chr2:231076246 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
263 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.942+675A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076246 | |||||||
| chr2:231076305 | G | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.943-729G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076305 | |||||||
| chr2:231076416 | C | T | 1 | a0001c0006t0002g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.943-618C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076416 | |||||||
| chr2:231076538 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.943-496A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076538 | |||||||
| chr2:231076540 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.943-494G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076540 | |||||||
| chr2:231076570 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.943-464C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076570 | |||||||
| chr2:231076904 | GAAAT | G | 11 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(8): Show |
11 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(8): Show |
intron_variant | MODIFIER | c.943-125_943-122del others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231076904 | ||||||
| chr2:231076908 | T | G | 1 | a0001c0001t0001g0332 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.943-126T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231076908 | |||||||
| chr2:231077016 | T | G | 1 | a0001c0001t0005g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.943-18T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 8/24 | chr2 | 231077016 | |||||||
| chr2:231077355 | T | C | 8 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071+193T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077355 | |||||||
| chr2:231077481 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1071+319G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077481 | |||||||
| chr2:231077698 | A | G | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1071+536A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077698 | |||||||
| chr2:231077778 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.1071+616G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077778 | |||||||
| chr2:231077810 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1071+648A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077810 | |||||||
| chr2:231077962 | T | A | 1 | a0001c0001t0001g0295 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1072-697T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077962 | |||||||
| chr2:231077968 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1072-691T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231077968 | |||||||
| chr2:231078005 | C | T | 2 | a0001c0001t0003g0166 a0001c0001t0003g0167 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1072-654C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078005 | |||||||
| chr2:231078160 | C | T | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1072-499C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078160 | |||||||
| chr2:231078376 | G | A | 7 | a0001c0001t0002g0013 a0001c0001t0002g0051 a0001c0001t0002g0052 others(4): Show |
7 | NA18966.hp1 NA19003.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1072-283G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078376 | |||||||
| chr2:231078426 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1072-233C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078426 | |||||||
| chr2:231078631 | T | G | 1 | a0001c0001t0003g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1072-28T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 9/24 | chr2 | 231078631 | |||||||
| chr2:231078791 | C | CT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0025 others(99): Show |
104 | HG00408.hp2 HG00558.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.1160+68dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr2 | 231078791 | ||||||
| chr2:231078791 | C | CTT | 13 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0264 others(10): Show |
13 | HG01109.hp1 HG02055.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160+67_1160+68dup others(2): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr2 | 231078791 | ||||||
| chr2:231078791 | CT | C | 8 | a0001c0001t0001g0331 a0001c0001t0002g0038 a0001c0001t0002g0039 others(5): Show |
8 | HG00438.hp1 HG01074.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160+68delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr2 | 231078791 | ||||||
| chr2:231079004 | A | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1160+257A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079004 | |||||||
| chr2:231079287 | T | C | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | NA18952.hp1 NA18957.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-249T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079287 | |||||||
| chr2:231079303 | T | G | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | NA18952.hp1 NA18957.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-233T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079303 | |||||||
| chr2:231079403 | A | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161-133A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079403 | |||||||
| chr2:231079477 | A | G | 1 | a0001c0001t0002g0055 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1161-59A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 10/24 | chr2 | 231079477 | |||||||
| chr2:231079659 | A | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.1239+45A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 11/24 | chr2 | 231079659 | |||||||
| chr2:231079973 | G | C | 1 | a0001c0001t0001g0332 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240-168G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 11/24 | chr2 | 231079973 | |||||||
| chr2:231080423 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1413+109A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080423 | |||||||
| chr2:231080586 | A | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(22): Show |
27 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1413+272A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080586 | |||||||
| chr2:231080706 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1413+392T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080706 | |||||||
| chr2:231080871 | G | A | 6 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(3): Show |
6 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413+557G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080871 | |||||||
| chr2:231080909 | G | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0339 |
3 | HG01070.hp2 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1413+595G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080909 | |||||||
| chr2:231080964 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1413+650G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231080964 | |||||||
| chr2:231081004 | C | A | 8 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1413+690C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081004 | |||||||
| chr2:231081144 | T | TA | 11 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0200 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413+852dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | ||||||
| chr2:231081144 | T | TAAAA | 8 | a0001c0001t0001g0169 a0001c0001t0001g0315 a0001c0001t0001g0316 others(5): Show |
8 | HG02027.hp2 HG02965.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1413+849_1413+852d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | ||||||
| chr2:231081144 | T | TAAAAA | 52 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(49): Show |
55 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1413+848_1413+852d others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | ||||||
| chr2:231081144 | T | TAAAAAA | 10 | a0001c0001t0001g0010 a0001c0001t0001g0212 a0001c0001t0001g0216 others(7): Show |
11 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413+847_1413+852d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | ||||||
| chr2:231081144 | TA | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0187 a0001c0001t0001g0230 others(13): Show |
16 | HG00323.hp1 HG01515.hp2 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.1413+852delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231081144 | ||||||
| chr2:231081170 | T | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413+856T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081170 | |||||||
| chr2:231081366 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413+1052C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081366 | |||||||
| chr2:231081418 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1413+1104T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081418 | |||||||
| chr2:231081518 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1413+1204G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081518 | |||||||
| chr2:231081573 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1413+1259G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081573 | |||||||
| chr2:231081594 | G | C | 1 | a0001c0001t0003g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1413+1280G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081594 | |||||||
| chr2:231081778 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1414-1105A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081778 | |||||||
| chr2:231081980 | C | A | 1 | a0001c0001t0001g0300 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1414-903C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231081980 | |||||||
| chr2:231082186 | C | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1414-697C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082186 | |||||||
| chr2:231082188 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1414-695G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082188 | |||||||
| chr2:231082256 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1414-627G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082256 | |||||||
| chr2:231082476 | G | A | 2 | a0001c0001t0003g0137 a0001c0001t0003g0139 |
2 | NA18963.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1414-407G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082476 | |||||||
| chr2:231082502 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
263 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.1414-381A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082502 | |||||||
| chr2:231082506 | A | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0350 |
3 | HG03490.hp1 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1414-377A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082506 | |||||||
| chr2:231082718 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1414-165C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082718 | |||||||
| chr2:231082753 | A | G | 4 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-130A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 12/24 | chr2 | 231082753 | |||||||
| chr2:231083054 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1525+60A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083054 | |||||||
| chr2:231083066 | C | G | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1525+72C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083066 | |||||||
| chr2:231083391 | A | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1526-176A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083391 | |||||||
| chr2:231083464 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1526-103A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 13/24 | chr2 | 231083464 | |||||||
| chr2:231083989 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1722+226C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231083989 | |||||||
| chr2:231084087 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1722+324G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084087 | |||||||
| chr2:231084114 | C | T | 1 | a0001c0001t0001g0314 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1722+351C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084114 | |||||||
| chr2:231084115 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1722+352G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084115 | |||||||
| chr2:231084220 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1722+457C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084220 | |||||||
| chr2:231084222 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1722+459G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084222 | |||||||
| chr2:231084284 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1722+521A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084284 | |||||||
| chr2:231084372 | T | A | 1 | a0001c0001t0003g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1722+609T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084372 | |||||||
| chr2:231084456 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1723-563C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084456 | |||||||
| chr2:231084465 | T | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1723-554T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084465 | |||||||
| chr2:231084537 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1723-482G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084537 | |||||||
| chr2:231084582 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1723-437G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084582 | |||||||
| chr2:231084584 | T | G | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1723-435T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084584 | |||||||
| chr2:231084855 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1723-164T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084855 | |||||||
| chr2:231084884 | A | G | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1723-135A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084884 | |||||||
| chr2:231084890 | A | G | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1723-129A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084890 | |||||||
| chr2:231084976 | G | C | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1723-43G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 14/24 | chr2 | 231084976 | |||||||
| chr2:231085232 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1818+118G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231085232 | |||||||
| chr2:231085674 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0331 a0001c0001t0001g0332 others(1): Show |
5 | HG00438.hp1 HG00558.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+560A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231085674 | |||||||
| chr2:231086009 | C | T | 1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1818+895C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086009 | |||||||
| chr2:231086093 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1818+979C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086093 | |||||||
| chr2:231086133 | T | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG01074.hp1 HG04204.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1819-984T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086133 | |||||||
| chr2:231086244 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1819-873G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086244 | |||||||
| chr2:231086368 | G | T | 11 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(8): Show |
11 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(8): Show |
intron_variant | MODIFIER | c.1819-749G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086368 | |||||||
| chr2:231086389 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1819-728G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086389 | |||||||
| chr2:231086529 | C | T | 5 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-588C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086529 | |||||||
| chr2:231086714 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1819-403G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 15/24 | chr2 | 231086714 | |||||||
| chr2:231087328 | A | C | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1883+147A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087328 | |||||||
| chr2:231087471 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1883+290C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087471 | |||||||
| chr2:231087777 | ACGGTGAA others(3): Show |
A | 1 | a0001c0001t0002g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1883+598_1883+607d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231087777 | ||||||
| chr2:231087897 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+716A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087897 | |||||||
| chr2:231087927 | A | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+746A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087927 | |||||||
| chr2:231087961 | T | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+780T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087961 | |||||||
| chr2:231087968 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1883+787A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087968 | |||||||
| chr2:231087984 | A | T | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+803A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231087984 | |||||||
| chr2:231088713 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1883+1532G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231088713 | |||||||
| chr2:231088718 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+1537A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231088718 | |||||||
| chr2:231089249 | A | G | 1 | a0002c0003t0003g0156 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1883+2068A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089249 | |||||||
| chr2:231089377 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
252 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1883+2196A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089377 | |||||||
| chr2:231089522 | T | C | 11 | a0001c0001t0002g0056 a0001c0001t0002g0060 a0001c0001t0002g0061 others(8): Show |
11 | HG00438.hp2 HG00609.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.1883+2341T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089522 | |||||||
| chr2:231089549 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
119 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1883+2368A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089549 | |||||||
| chr2:231089594 | G | GAT | 14 | a0001c0001t0001g0172 a0001c0001t0001g0233 a0001c0001t0001g0246 others(11): Show |
14 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1883+2432_1883+243 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | ||||||
| chr2:231089594 | G | GATATATA others(7): Show |
1 | a0001c0002t0004g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1883+2420_1883+243 others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | ||||||
| chr2:231089594 | G | GATATATA others(9): Show |
1 | a0001c0002t0004g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1883+2418_1883+243 others(20): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | ||||||
| chr2:231089594 | G | GATATATA others(37): Show |
1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1883+2433_1883+243 others(48): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | ||||||
| chr2:231089594 | G | GATATATA others(45): Show |
1 | a0001c0002t0004g0030 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1883+2433_1883+243 others(56): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | ||||||
| chr2:231089594 | G | GATATATA others(49): Show |
1 | a0001c0002t0004g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1883+2433_1883+243 others(60): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231089594 | ||||||
| chr2:231089917 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+2736C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089917 | |||||||
| chr2:231089924 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1883+2743A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231089924 | |||||||
| chr2:231090176 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1883+2995C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090176 | |||||||
| chr2:231090312 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1883+3131G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090312 | |||||||
| chr2:231090331 | C | A | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0118 others(53): Show |
58 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1883+3150C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090331 | |||||||
| chr2:231090565 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+3384A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090565 | |||||||
| chr2:231090609 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1883+3428C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090609 | |||||||
| chr2:231090623 | G | T | 1 | a0001c0001t0003g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1883+3442G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090623 | |||||||
| chr2:231090690 | T | G | 7 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+3509T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090690 | |||||||
| chr2:231090831 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1883+3650C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231090831 | |||||||
| chr2:231091195 | G | C | 2 | a0001c0001t0003g0145 a0001c0001t0003g0146 |
2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1883+4014G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091195 | |||||||
| chr2:231091209 | C | T | 1 | a0001c0001t0002g0040 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1883+4028C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091209 | |||||||
| chr2:231091772 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1883+4591C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091772 | |||||||
| chr2:231091838 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+4657G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091838 | |||||||
| chr2:231091903 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1883+4722C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231091903 | |||||||
| chr2:231092038 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1883+4857A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092038 | |||||||
| chr2:231092215 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1883+5034G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092215 | |||||||
| chr2:231092547 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1883+5366C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092547 | |||||||
| chr2:231092579 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+5398G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092579 | |||||||
| chr2:231092610 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1883+5429G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092610 | |||||||
| chr2:231092616 | C | A | 1 | a0001c0001t0005g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1883+5435C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092616 | |||||||
| chr2:231092734 | G | T | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+5553G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231092734 | |||||||
| chr2:231093311 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG03453.hp2 HG03471.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+6130A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093311 | |||||||
| chr2:231093398 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1883+6217C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093398 | |||||||
| chr2:231093401 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1883+6220G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093401 | |||||||
| chr2:231093424 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1883+6243C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093424 | |||||||
| chr2:231093425 | G | A | 6 | a0001c0001t0002g0110 a0001c0002t0004g0026 a0001c0002t0004g0027 others(3): Show |
6 | HG02280.hp1 HG02683.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1883+6244G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093425 | |||||||
| chr2:231093433 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1883+6252C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093433 | |||||||
| chr2:231093478 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1883+6297A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231093478 | |||||||
| chr2:231094157 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1883+6976G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094157 | |||||||
| chr2:231094165 | C | A | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1883+6984C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094165 | |||||||
| chr2:231094325 | T | C | 1 | a0001c0001t0002g0349 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1883+7144T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094325 | |||||||
| chr2:231094583 | G | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+7402G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094583 | |||||||
| chr2:231094681 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0001g0327 others(3): Show |
7 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+7500G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231094681 | |||||||
| chr2:231095054 | G | A | 7 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+7873G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095054 | |||||||
| chr2:231095104 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1883+7923A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095104 | |||||||
| chr2:231095111 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+7930T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095111 | |||||||
| chr2:231095275 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1883+8094T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095275 | |||||||
| chr2:231095584 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1883+8403G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095584 | |||||||
| chr2:231095862 | G | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+8681G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095862 | |||||||
| chr2:231095864 | C | G | 1 | a0001c0001t0001g0248 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1883+8683C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095864 | |||||||
| chr2:231095882 | G | A | 8 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG01361.hp2 NA18942.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.1883+8701G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095882 | |||||||
| chr2:231095910 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1883+8729A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231095910 | |||||||
| chr2:231096028 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1883+8847A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096028 | |||||||
| chr2:231096127 | T | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+8946T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096127 | |||||||
| chr2:231096192 | A | G | 2 | a0001c0001t0003g0165 a0001c0001t0003g0168 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1883+9011A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096192 | |||||||
| chr2:231096455 | G | C | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+9274G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096455 | |||||||
| chr2:231096480 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0179 a0001c0001t0001g0180 others(8): Show |
12 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1883+9299C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096480 | |||||||
| chr2:231096569 | A | T | 1 | a0001c0001t0001g0008 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1883+9388A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096569 | |||||||
| chr2:231096793 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+9612G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096793 | |||||||
| chr2:231096868 | G | T | 46 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0120 others(43): Show |
48 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1883+9687G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096868 | |||||||
| chr2:231096876 | A | T | 1 | a0001c0001t0001g0314 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1883+9695A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231096876 | |||||||
| chr2:231097299 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1883+10118T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097299 | |||||||
| chr2:231097341 | T | C | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+10160T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097341 | |||||||
| chr2:231097432 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+10251T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097432 | |||||||
| chr2:231097451 | T | C | 1 | a0001c0001t0003g0130 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1883+10270T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097451 | |||||||
| chr2:231097574 | G | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+10393G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097574 | |||||||
| chr2:231097651 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1883+10470C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097651 | |||||||
| chr2:231097771 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1883+10590G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231097771 | |||||||
| chr2:231098002 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1883+10821G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098002 | |||||||
| chr2:231098025 | C | G | 4 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+10844C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098025 | |||||||
| chr2:231098058 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1883+10877G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098058 | |||||||
| chr2:231098078 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1883+10897C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098078 | |||||||
| chr2:231098094 | G | T | 2 | a0001c0001t0001g0345 a0001c0001t0001g0347 |
2 | HG01069.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1883+10913G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098094 | |||||||
| chr2:231098349 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1883+11168A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098349 | |||||||
| chr2:231098361 | CT | C | 4 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0347 others(1): Show |
4 | HG00280.hp2 HG01069.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1883+11183delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098361 | ||||||
| chr2:231098402 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1883+11221T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098402 | |||||||
| chr2:231098447 | TTC | T | 6 | a0001c0001t0003g0005 a0001c0001t0003g0137 a0001c0001t0003g0138 others(3): Show |
7 | HG03834.hp2 NA18963.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+11278_1883+11 others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098447 | ||||||
| chr2:231098457 | CTCTG | C | 4 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0003g0334 others(1): Show |
4 | HG02145.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+11280_1883+11 others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098457 | ||||||
| chr2:231098461 | G | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+11280G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098461 | |||||||
| chr2:231098512 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1883+11331T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098512 | |||||||
| chr2:231098543 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+11362T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098543 | |||||||
| chr2:231098555 | TTCTCTC | T | 3 | a0001c0001t0002g0042 a0001c0001t0002g0099 a0001c0005t0001g0031 |
3 | NA18973.hp1 NA18985.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1883+11391_1883+11 others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231098555 | ||||||
| chr2:231098780 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1883+11599G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231098780 | |||||||
| chr2:231099061 | C | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+11880C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099061 | |||||||
| chr2:231099075 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1883+11894G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099075 | |||||||
| chr2:231099180 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
14 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1883+11999C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099180 | |||||||
| chr2:231099181 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+12000G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099181 | |||||||
| chr2:231099335 | T | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+12154T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099335 | |||||||
| chr2:231099396 | G | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+12215G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099396 | |||||||
| chr2:231099443 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+12262C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099443 | |||||||
| chr2:231099473 | C | G | 1 | a0001c0001t0001g0324 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1883+12292C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099473 | |||||||
| chr2:231099813 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+12632T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099813 | |||||||
| chr2:231099859 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1883+12678C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099859 | |||||||
| chr2:231099946 | C | T | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+12765C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231099946 | |||||||
| chr2:231100129 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1883+12948G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100129 | |||||||
| chr2:231100151 | C | T | 3 | a0001c0001t0001g0299 a0001c0001t0001g0311 a0001c0001t0001g0312 |
3 | HG01928.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1883+12970C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100151 | |||||||
| chr2:231100171 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+12990T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100171 | |||||||
| chr2:231100180 | T | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+12999T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100180 | |||||||
| chr2:231100250 | T | C | 2 | a0001c0001t0003g0351 a0001c0001t0003g0352 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1883+13069T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100250 | |||||||
| chr2:231100280 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1883+13099A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100280 | |||||||
| chr2:231100351 | G | A | 58 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(55): Show |
60 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1883+13170G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100351 | |||||||
| chr2:231100380 | C | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+13199C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100380 | |||||||
| chr2:231100380 | C | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1883+13199C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100380 | |||||||
| chr2:231100491 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+13310G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100491 | |||||||
| chr2:231100698 | A | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0339 |
3 | HG01070.hp2 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1883+13517A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100698 | |||||||
| chr2:231100891 | C | G | 1 | a0001c0001t0001g0224 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1883+13710C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231100891 | |||||||
| chr2:231101109 | T | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+13928T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101109 | |||||||
| chr2:231101379 | A | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0350 |
3 | HG03490.hp1 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1883+14198A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101379 | |||||||
| chr2:231101442 | T | C | 6 | a0001c0001t0002g0036 a0001c0001t0003g0134 a0001c0001t0003g0135 others(3): Show |
6 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1883+14261T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101442 | |||||||
| chr2:231101569 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+14388T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101569 | |||||||
| chr2:231101592 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+14411A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101592 | |||||||
| chr2:231101752 | C | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+14571C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231101752 | |||||||
| chr2:231102426 | A | G | 1 | a0001c0001t0001g0007 | 2 | NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1883+15245A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102426 | |||||||
| chr2:231102496 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1883+15315A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102496 | |||||||
| chr2:231102524 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1883+15343A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102524 | |||||||
| chr2:231102780 | T | A | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+15599T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102780 | |||||||
| chr2:231102873 | GTTATATT others(16): Show |
G | 6 | a0001c0001t0001g0216 a0001c0001t0001g0282 a0001c0001t0003g0158 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1883+15715_1883+15 others(29): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231102873 | ||||||
| chr2:231102896 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
252 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1883+15715A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102896 | |||||||
| chr2:231102969 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0003g0155 |
2 | HG02155.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1883+15788C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102969 | |||||||
| chr2:231102976 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0194 others(81): Show |
86 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.1883+15795T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231102976 | |||||||
| chr2:231103172 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1883+15991T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231103172 | |||||||
| chr2:231103235 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1883+16054C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231103235 | |||||||
| chr2:231103518 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1883+16337G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231103518 | |||||||
| chr2:231104057 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1883+16876G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104057 | |||||||
| chr2:231104101 | A | AGTT | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1883+16921_1883+16 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231104101 | ||||||
| chr2:231104206 | G | T | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1883+17025G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104206 | |||||||
| chr2:231104333 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+17152C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104333 | |||||||
| chr2:231104336 | CT | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+17157delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231104336 | ||||||
| chr2:231104367 | T | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0004g0026 others(5): Show |
8 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1883+17186T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104367 | |||||||
| chr2:231104368 | A | G | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+17187A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104368 | |||||||
| chr2:231104405 | A | G | 2 | a0001c0001t0003g0004 a0001c0001t0003g0122 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1883+17224A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104405 | |||||||
| chr2:231104438 | A | G | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+17257A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104438 | |||||||
| chr2:231104550 | C | CT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0194 others(79): Show |
84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.1883+17370dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231104550 | ||||||
| chr2:231104576 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1883+17395C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104576 | |||||||
| chr2:231104612 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1883+17431G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104612 | |||||||
| chr2:231104669 | C | T | 1 | a0001c0001t0003g0154 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1883+17488C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104669 | |||||||
| chr2:231104734 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1883+17553C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104734 | |||||||
| chr2:231104754 | C | T | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+17573C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104754 | |||||||
| chr2:231104840 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1883+17659A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104840 | |||||||
| chr2:231104942 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0342 |
2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1883+17761G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104942 | |||||||
| chr2:231104965 | G | A | 1 | a0001c0001t0002g0342 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1883+17784G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231104965 | |||||||
| chr2:231105222 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1883+18041T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105222 | |||||||
| chr2:231105322 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1883+18141G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105322 | |||||||
| chr2:231105455 | G | C | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1883+18274G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105455 | |||||||
| chr2:231105648 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1883+18467G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105648 | |||||||
| chr2:231105794 | CCACTAAC others(5): Show |
C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+18621_1883+18 others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231105794 | ||||||
| chr2:231105911 | T | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | HG01346.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1883+18730T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231105911 | |||||||
| chr2:231105954 | A | AT | 45 | a0001c0001t0001g0087 a0001c0001t0001g0250 a0001c0001t0001g0262 others(42): Show |
46 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1883+18783dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231105954 | ||||||
| chr2:231106018 | G | GT | 8 | a0001c0001t0001g0024 a0001c0001t0002g0054 a0001c0001t0002g0083 others(5): Show |
8 | HG01981.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1883+18852dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231106018 | ||||||
| chr2:231106018 | GT | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
248 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1883+18852delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231106018 | ||||||
| chr2:231106024 | T | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0266 others(1): Show |
4 | HG03688.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+18843T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231106024 | |||||||
| chr2:231106207 | T | A | 1 | a0001c0001t0001g0311 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1883+19026T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231106207 | |||||||
| chr2:231106960 | C | A | 1 | a0001c0001t0003g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1883+19779C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231106960 | |||||||
| chr2:231107089 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1883+19908G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107089 | |||||||
| chr2:231107144 | A | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+19963A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107144 | |||||||
| chr2:231107208 | A | C | 1 | a0001c0001t0002g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1883+20027A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107208 | |||||||
| chr2:231107461 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0194 others(78): Show |
83 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.1883+20280A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107461 | |||||||
| chr2:231107683 | G | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+20502G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107683 | |||||||
| chr2:231107829 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG01243.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1883+20648C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107829 | |||||||
| chr2:231107870 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1883+20689T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231107870 | |||||||
| chr2:231108649 | G | A | 6 | a0001c0001t0001g0025 a0001c0002t0004g0026 a0001c0002t0004g0027 others(3): Show |
6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1883+21468G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108649 | |||||||
| chr2:231108688 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1883+21507A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108688 | |||||||
| chr2:231108702 | T | C | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+21521T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108702 | |||||||
| chr2:231108711 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+21530G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108711 | |||||||
| chr2:231108732 | G | A | 1 | a0001c0001t0002g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1883+21551G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108732 | |||||||
| chr2:231108991 | C | G | 1 | a0001c0001t0002g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1883+21810C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231108991 | |||||||
| chr2:231109120 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1883+21939C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109120 | |||||||
| chr2:231109341 | C | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02258.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1883+22160C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109341 | |||||||
| chr2:231109535 | A | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0245 others(4): Show |
9 | NA18951.hp1 NA18955.hp1 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1883+22354A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109535 | |||||||
| chr2:231109548 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1883+22367C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109548 | |||||||
| chr2:231109654 | A | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+22473A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231109654 | |||||||
| chr2:231110209 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1883+23028A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110209 | |||||||
| chr2:231110755 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1883+23574A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110755 | |||||||
| chr2:231110831 | A | G | 5 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0099 others(2): Show |
5 | NA18957.hp2 NA18967.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+23650A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110831 | |||||||
| chr2:231110832 | C | G | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 |
3 | NA18952.hp1 NA18957.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1883+23651C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110832 | |||||||
| chr2:231110868 | T | C | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+23687T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231110868 | |||||||
| chr2:231111329 | A | C | 1 | a0001c0001t0002g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1883+24148A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111329 | |||||||
| chr2:231111746 | T | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1883+24565T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111746 | |||||||
| chr2:231111865 | G | A | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+24684G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111865 | |||||||
| chr2:231111901 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1883+24720A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111901 | |||||||
| chr2:231111947 | G | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1883+24766G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231111947 | |||||||
| chr2:231112117 | C | T | 2 | a0001c0001t0003g0165 a0001c0001t0003g0168 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1883+24936C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112117 | |||||||
| chr2:231112227 | A | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | NA18979.hp2 NA18988.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1883+25046A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112227 | |||||||
| chr2:231112254 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1883+25073C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112254 | |||||||
| chr2:231112288 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1883+25107C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112288 | |||||||
| chr2:231112382 | T | C | 1 | a0001c0001t0003g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1883+25201T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112382 | |||||||
| chr2:231112516 | C | T | 3 | a0001c0002t0004g0027 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+25335C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112516 | |||||||
| chr2:231112600 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1883+25419A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112600 | |||||||
| chr2:231112723 | G | A | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1883+25542G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112723 | |||||||
| chr2:231112725 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1883+25544A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112725 | |||||||
| chr2:231112779 | A | T | 1 | a0001c0001t0003g0153 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1883+25598A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112779 | |||||||
| chr2:231112813 | C | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1883+25632C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112813 | |||||||
| chr2:231112816 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1883+25635A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112816 | |||||||
| chr2:231112821 | CT | C | 7 | a0001c0001t0001g0024 a0001c0002t0004g0026 a0001c0002t0004g0027 others(4): Show |
7 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1883+25641delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112821 | |||||||
| chr2:231112914 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1883+25733C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112914 | |||||||
| chr2:231112992 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1884-25744C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231112992 | |||||||
| chr2:231113089 | G | A | 2 | a0001c0001t0003g0165 a0001c0001t0003g0168 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1884-25647G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113089 | |||||||
| chr2:231113149 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1884-25587G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113149 | |||||||
| chr2:231113262 | A | G | 2 | a0001c0001t0001g0328 a0001c0001t0001g0330 |
2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1884-25474A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113262 | |||||||
| chr2:231113285 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-25451C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113285 | |||||||
| chr2:231113495 | T | C | 1 | a0001c0001t0002g0349 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1884-25241T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113495 | |||||||
| chr2:231113961 | A | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-24775A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231113961 | |||||||
| chr2:231114359 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0005t0001g0031 |
3 | NA20129.hp2 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1884-24377G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114359 | |||||||
| chr2:231114531 | G | A | 3 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 |
3 | HG01069.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1884-24205G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114531 | |||||||
| chr2:231114544 | A | G | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-24192A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114544 | |||||||
| chr2:231114567 | T | C | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-24169T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114567 | |||||||
| chr2:231114641 | C | T | 41 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(38): Show |
43 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1884-24095C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114641 | |||||||
| chr2:231114806 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1884-23930T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114806 | |||||||
| chr2:231114834 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1884-23902A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231114834 | |||||||
| chr2:231115150 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1884-23586T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115150 | |||||||
| chr2:231115162 | G | A | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1884-23574G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115162 | |||||||
| chr2:231115280 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-23456C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115280 | |||||||
| chr2:231115305 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1884-23431C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115305 | |||||||
| chr2:231115493 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1884-23243G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115493 | |||||||
| chr2:231115716 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-23020A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115716 | |||||||
| chr2:231115720 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1884-23016G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115720 | |||||||
| chr2:231115860 | C | G | 1 | a0001c0001t0001g0250 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1884-22876C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231115860 | |||||||
| chr2:231116063 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(197): Show |
208 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1884-22673A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116063 | |||||||
| chr2:231116154 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1884-22582A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116154 | |||||||
| chr2:231116326 | C | G | 1 | a0001c0001t0002g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1884-22410C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116326 | |||||||
| chr2:231116390 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-22346A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116390 | |||||||
| chr2:231116393 | T | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-22343T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116393 | |||||||
| chr2:231116429 | G | C | 1 | a0001c0001t0002g0059 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1884-22307G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116429 | |||||||
| chr2:231116433 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1884-22303C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116433 | |||||||
| chr2:231116507 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1884-22229G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116507 | |||||||
| chr2:231116605 | A | G | 1 | a0002c0003t0002g0081 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1884-22131A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116605 | |||||||
| chr2:231116645 | G | GT | 17 | a0001c0001t0001g0025 a0001c0001t0003g0118 a0001c0001t0003g0119 others(14): Show |
17 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1884-22085dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231116645 | ||||||
| chr2:231116662 | T | A | 1 | a0001c0002t0004g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884-22074T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116662 | |||||||
| chr2:231116747 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-21989A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116747 | |||||||
| chr2:231116790 | A | T | 1 | a0001c0001t0001g0225 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1884-21946A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231116790 | |||||||
| chr2:231117062 | A | G | 7 | a0001c0001t0002g0013 a0001c0001t0002g0051 a0001c0001t0002g0052 others(4): Show |
7 | NA18966.hp1 NA19003.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-21674A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117062 | |||||||
| chr2:231117119 | A | C | 1 | a0001c0001t0001g0247 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1884-21617A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117119 | |||||||
| chr2:231117182 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1884-21554G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117182 | |||||||
| chr2:231117196 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-21540T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117196 | |||||||
| chr2:231117249 | A | G | 1 | a0001c0001t0003g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1884-21487A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117249 | |||||||
| chr2:231117278 | A | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(332): Show |
347 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(344): Show |
intron_variant | MODIFIER | c.1884-21458A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117278 | |||||||
| chr2:231117669 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1884-21067T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117669 | |||||||
| chr2:231117791 | C | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1884-20945C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231117791 | |||||||
| chr2:231118033 | T | C | 3 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02258.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1884-20703T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118033 | |||||||
| chr2:231118112 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1884-20624G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118112 | |||||||
| chr2:231118124 | T | TAATAGTA others(278): Show |
7 | a0001c0001t0003g0119 a0001c0001t0003g0123 a0001c0001t0003g0124 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-20597_1884-20 others(291): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118124 | ||||||
| chr2:231118124 | T | TAATAGTA others(279): Show |
3 | a0001c0001t0003g0118 a0001c0001t0003g0125 a0001c0001t0003g0129 |
3 | HG02055.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1884-20597_1884-20 others(292): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118124 | ||||||
| chr2:231118236 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-20500T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118236 | |||||||
| chr2:231118257 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0177 a0001c0001t0001g0178 |
4 | NA18940.hp1 NA18973.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-20479A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118257 | |||||||
| chr2:231118295 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-20441C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118295 | |||||||
| chr2:231118437 | G | GT | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-20297dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118437 | ||||||
| chr2:231118461 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-20275G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118461 | |||||||
| chr2:231118525 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0336 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1884-20211G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118525 | |||||||
| chr2:231118668 | T | G | 32 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(29): Show |
34 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1884-20068T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118668 | |||||||
| chr2:231118729 | A | G | 1 | a0001c0001t0003g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1884-20007A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231118729 | |||||||
| chr2:231118978 | AAAAG | A | 69 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1884-19752_1884-19 others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231118978 | ||||||
| chr2:231119110 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1884-19626A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119110 | |||||||
| chr2:231119436 | T | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-19300T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119436 | |||||||
| chr2:231119439 | C | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-19297C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119439 | |||||||
| chr2:231119504 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1884-19232C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119504 | |||||||
| chr2:231119514 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0267 |
2 | HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1884-19222A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119514 | |||||||
| chr2:231119651 | A | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0266 others(1): Show |
4 | HG03688.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-19085A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119651 | |||||||
| chr2:231119869 | C | CA | 27 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0022 others(24): Show |
27 | HG00438.hp2 HG01071.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1884-18845dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | ||||||
| chr2:231119869 | CA | C | 37 | a0001c0001t0001g0179 a0001c0001t0001g0184 a0001c0001t0001g0189 others(34): Show |
37 | HG00673.hp2 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.1884-18845delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | ||||||
| chr2:231119869 | CAA | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
213 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1884-18846_1884-18 others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | ||||||
| chr2:231119869 | CAAA | C | 7 | a0001c0001t0001g0310 a0001c0001t0003g0159 a0001c0002t0004g0026 others(4): Show |
7 | HG01169.hp1 HG02083.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-18847_1884-18 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119869 | ||||||
| chr2:231119950 | C | CT | 7 | a0001c0001t0001g0178 a0001c0001t0001g0265 a0001c0001t0001g0303 others(4): Show |
7 | HG00735.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-18770dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119950 | ||||||
| chr2:231119950 | CT | C | 6 | a0001c0001t0002g0062 a0001c0001t0002g0064 a0001c0001t0002g0067 others(3): Show |
6 | HG00438.hp2 HG00609.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1884-18770delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119950 | ||||||
| chr2:231119966 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-18770T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231119966 | |||||||
| chr2:231119984 | AC | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-18748delC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231119984 | ||||||
| chr2:231120241 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1884-18495C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120241 | |||||||
| chr2:231120242 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-18494G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120242 | |||||||
| chr2:231120457 | AC | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0339 |
3 | HG01070.hp2 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1884-18278delC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120457 | |||||||
| chr2:231120542 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1884-18194A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120542 | |||||||
| chr2:231120543 | A | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-18193A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120543 | |||||||
| chr2:231120562 | A | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1884-18174A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120562 | |||||||
| chr2:231120822 | C | T | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0267 |
3 | HG01928.hp1 HG02300.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1884-17914C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120822 | |||||||
| chr2:231120827 | G | A | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884-17909G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231120827 | |||||||
| chr2:231121396 | TAATAAAC others(6): Show |
T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0093 |
3 | NA18988.hp2 NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1884-17337_1884-17 others(19): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231121396 | ||||||
| chr2:231121740 | A | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-16996A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121740 | |||||||
| chr2:231121979 | A | G | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16757A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121979 | |||||||
| chr2:231121980 | T | C | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16756T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121980 | |||||||
| chr2:231121981 | C | CTGTACAG | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16755_1884-16 others(13): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121981 | |||||||
| chr2:231121982 | A | T | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16754A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121982 | |||||||
| chr2:231121984 | A | C | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1884-16752A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231121984 | |||||||
| chr2:231122018 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-16718T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231122018 | |||||||
| chr2:231122442 | A | C | 1 | a0001c0001t0003g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1884-16294A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231122442 | |||||||
| chr2:231122494 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-16242A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231122494 | |||||||
| chr2:231122766 | AGGAACAC others(4): Show |
A | 1 | a0001c0001t0001g0250 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1884-15968_1884-15 others(17): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231122766 | ||||||
| chr2:231123014 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1884-15722G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123014 | |||||||
| chr2:231123037 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0179 a0001c0001t0001g0181 others(7): Show |
11 | HG00544.hp2 HG00673.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1884-15699C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123037 | |||||||
| chr2:231123122 | A | G | 1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1884-15614A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123122 | |||||||
| chr2:231123176 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-15560T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123176 | |||||||
| chr2:231123241 | C | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1884-15495C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123241 | |||||||
| chr2:231123386 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-15350A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123386 | |||||||
| chr2:231123388 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1884-15348G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123388 | |||||||
| chr2:231123613 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-15123C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123613 | |||||||
| chr2:231123638 | T | C | 1 | a0001c0001t0006g0279 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1884-15098T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123638 | |||||||
| chr2:231123674 | A | G | 7 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884-15062A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123674 | |||||||
| chr2:231123910 | C | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0278 |
2 | NA18943.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1884-14826C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123910 | |||||||
| chr2:231123912 | A | G | 2 | a0001c0001t0003g0004 a0001c0001t0003g0122 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1884-14824A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231123912 | |||||||
| chr2:231124099 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0342 |
2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1884-14637C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124099 | |||||||
| chr2:231124141 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0194 others(77): Show |
82 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.1884-14595A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124141 | |||||||
| chr2:231124347 | C | G | 1 | a0001c0001t0001g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1884-14389C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124347 | |||||||
| chr2:231124933 | C | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1884-13803C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231124933 | |||||||
| chr2:231125321 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1884-13415T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125321 | |||||||
| chr2:231125386 | A | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0194 others(79): Show |
84 | HG00408.hp2 HG00558.hp2 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.1884-13350A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125386 | |||||||
| chr2:231125657 | A | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(196): Show |
207 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1884-13079A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125657 | |||||||
| chr2:231125734 | A | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0262 |
3 | NA18952.hp2 NA19077.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1884-13002A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125734 | |||||||
| chr2:231125761 | A | C | 1 | a0001c0001t0002g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1884-12975A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125761 | |||||||
| chr2:231125953 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1884-12783G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231125953 | |||||||
| chr2:231126135 | G | T | 2 | a0001c0001t0003g0132 a0001c0001t0003g0133 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1884-12601G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126135 | |||||||
| chr2:231126152 | C | T | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1884-12584C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126152 | |||||||
| chr2:231126244 | C | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0093 |
3 | NA18988.hp2 NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1884-12492C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126244 | |||||||
| chr2:231126304 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1884-12432G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126304 | |||||||
| chr2:231126609 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1884-12127A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126609 | |||||||
| chr2:231126638 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1884-12098A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126638 | |||||||
| chr2:231126808 | G | A | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884-11928G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126808 | |||||||
| chr2:231126850 | T | C | 1 | a0001c0001t0002g0016 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1884-11886T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126850 | |||||||
| chr2:231126903 | T | A | 7 | a0001c0001t0003g0142 a0001c0001t0003g0150 a0001c0001t0003g0151 others(4): Show |
7 | NA18972.hp1 NA18975.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884-11833T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231126903 | |||||||
| chr2:231127028 | C | T | 7 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884-11708C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127028 | |||||||
| chr2:231127052 | C | T | 1 | a0001c0001t0003g0352 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1884-11684C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127052 | |||||||
| chr2:231127274 | C | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0342 a0001c0002t0004g0029 |
3 | HG03139.hp1 NA18983.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1884-11462C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127274 | |||||||
| chr2:231127274 | C | CA | 11 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0200 others(8): Show |
11 | HG00438.hp2 HG01070.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1884-11448dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231127274 | ||||||
| chr2:231127277 | A | C | 2 | a0001c0001t0001g0011 a0001c0001t0003g0120 |
3 | NA18522.hp2 NA19002.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1884-11459A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127277 | |||||||
| chr2:231127288 | AC | A | 4 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0142 others(1): Show |
4 | NA18951.hp2 NA18972.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1884-11447delC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127288 | |||||||
| chr2:231127289 | C | A | 30 | a0001c0001t0003g0005 a0001c0001t0003g0134 a0001c0001t0003g0135 others(27): Show |
31 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1884-11447C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127289 | |||||||
| chr2:231127499 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1884-11237C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127499 | |||||||
| chr2:231127500 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1884-11236G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127500 | |||||||
| chr2:231127543 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-11193C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127543 | |||||||
| chr2:231127597 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1884-11139G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127597 | |||||||
| chr2:231127600 | T | C | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1884-11136T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127600 | |||||||
| chr2:231127630 | G | A | 1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1884-11106G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231127630 | |||||||
| chr2:231128054 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1884-10682A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128054 | |||||||
| chr2:231128092 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0327 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1884-10644G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128092 | |||||||
| chr2:231128092 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1884-10644G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128092 | |||||||
| chr2:231128231 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-10505T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128231 | |||||||
| chr2:231128234 | T | C | 1 | a0001c0001t0002g0052 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1884-10502T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128234 | |||||||
| chr2:231128264 | A | G | 1 | a0002c0003t0002g0081 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1884-10472A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128264 | |||||||
| chr2:231128324 | A | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1884-10412A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128324 | |||||||
| chr2:231128352 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-10384C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128352 | |||||||
| chr2:231128473 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1884-10263A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128473 | |||||||
| chr2:231128484 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-10252G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128484 | |||||||
| chr2:231128525 | C | T | 6 | a0001c0001t0003g0352 a0001c0002t0004g0026 a0001c0002t0004g0027 others(3): Show |
6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1884-10211C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128525 | |||||||
| chr2:231128598 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1884-10138A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231128598 | |||||||
| chr2:231129024 | G | T | 36 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(33): Show |
38 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1884-9712G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129024 | |||||||
| chr2:231129048 | T | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-9688T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129048 | |||||||
| chr2:231129332 | T | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-9404T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129332 | |||||||
| chr2:231129479 | A | G | 2 | a0001c0001t0003g0137 a0001c0001t0003g0139 |
2 | NA18963.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1884-9257A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129479 | |||||||
| chr2:231129666 | A | G | 1 | a0001c0001t0002g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1884-9070A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129666 | |||||||
| chr2:231129747 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0222 a0001c0001t0001g0227 |
3 | NA18947.hp2 NA18950.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1884-8989A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129747 | |||||||
| chr2:231129879 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1884-8857A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231129879 | |||||||
| chr2:231130088 | G | A | 2 | a0001c0001t0003g0142 a0001c0001t0003g0161 |
2 | NA18972.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1884-8648G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231130088 | |||||||
| chr2:231130580 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1884-8156C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231130580 | |||||||
| chr2:231130887 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1884-7849G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231130887 | |||||||
| chr2:231131018 | G | T | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1884-7718G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131018 | |||||||
| chr2:231131056 | G | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1884-7680G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131056 | |||||||
| chr2:231131462 | TAGAAAGT others(317): Show |
T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1884-7254_1884-693 others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231131462 | ||||||
| chr2:231131761 | C | CA | 19 | a0001c0001t0001g0087 a0001c0001t0002g0018 a0001c0001t0002g0019 others(16): Show |
19 | HG00423.hp2 HG00438.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1884-6949dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231131761 | ||||||
| chr2:231131761 | CA | C | 9 | a0001c0001t0002g0043 a0001c0001t0002g0071 a0001c0001t0002g0072 others(6): Show |
9 | HG00323.hp1 HG00639.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1884-6949delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231131761 | ||||||
| chr2:231131851 | A | G | 1 | a0001c0006t0002g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1884-6885A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131851 | |||||||
| chr2:231131862 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.1884-6874G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231131862 | |||||||
| chr2:231132076 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1884-6660T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132076 | |||||||
| chr2:231132095 | C | G | 69 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1884-6641C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132095 | |||||||
| chr2:231132241 | A | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1884-6495A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132241 | |||||||
| chr2:231132618 | G | GC | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0266 others(1): Show |
4 | HG03688.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-6117dupC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231132618 | ||||||
| chr2:231132624 | A | G | 18 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(15): Show |
18 | HG01243.hp1 HG02055.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1884-6112A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132624 | |||||||
| chr2:231132896 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1884-5840C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231132896 | |||||||
| chr2:231133106 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1884-5630A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133106 | |||||||
| chr2:231133234 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-5502G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133234 | |||||||
| chr2:231133245 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-5491C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133245 | |||||||
| chr2:231133273 | C | T | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-5463C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133273 | |||||||
| chr2:231133296 | G | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-5440G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133296 | |||||||
| chr2:231133383 | C | T | 1 | a0001c0001t0003g0334 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1884-5353C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133383 | |||||||
| chr2:231133416 | G | A | 5 | a0001c0001t0001g0025 a0001c0002t0004g0026 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03139.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-5320G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133416 | |||||||
| chr2:231133581 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1884-5155C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231133581 | |||||||
| chr2:231134139 | A | G | 1 | a0001c0001t0002g0003 | 2 | NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1884-4597A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231134139 | |||||||
| chr2:231134322 | G | A | 3 | a0001c0001t0003g0158 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG01168.hp1 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1884-4414G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231134322 | |||||||
| chr2:231134733 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0104 |
2 | HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1884-4003G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231134733 | |||||||
| chr2:231135057 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1884-3679A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135057 | |||||||
| chr2:231135110 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1884-3626T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135110 | |||||||
| chr2:231135113 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-3623A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135113 | |||||||
| chr2:231135164 | G | C | 8 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1884-3572G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135164 | |||||||
| chr2:231135175 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1884-3561G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135175 | |||||||
| chr2:231135186 | G | T | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1884-3550G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135186 | |||||||
| chr2:231135350 | G | A | 4 | a0001c0001t0001g0304 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | NA18943.hp1 NA18975.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1884-3386G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135350 | |||||||
| chr2:231135443 | G | A | 6 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0091 others(3): Show |
6 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1884-3293G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135443 | |||||||
| chr2:231135701 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0226 |
3 | HG03490.hp2 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1884-3035A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135701 | |||||||
| chr2:231135831 | A | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1884-2905A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135831 | |||||||
| chr2:231135999 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0177 |
3 | NA18940.hp1 NA18973.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1884-2737G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231135999 | |||||||
| chr2:231136219 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1884-2517C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136219 | |||||||
| chr2:231136227 | T | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1884-2509T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136227 | |||||||
| chr2:231136535 | A | G | 1 | a0001c0001t0003g0137 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1884-2201A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136535 | |||||||
| chr2:231136807 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-1929A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136807 | |||||||
| chr2:231136969 | ATT | A | 7 | a0001c0001t0003g0142 a0001c0001t0003g0150 a0001c0001t0003g0151 others(4): Show |
7 | NA18972.hp1 NA18975.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884-1766_1884-176 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231136969 | |||||||
| chr2:231137057 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1884-1679A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137057 | |||||||
| chr2:231137148 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1884-1588C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137148 | |||||||
| chr2:231137211 | G | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1884-1525G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137211 | |||||||
| chr2:231137412 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1884-1324C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137412 | |||||||
| chr2:231137424 | A | T | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1884-1312A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137424 | |||||||
| chr2:231137487 | A | G | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884-1249A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137487 | |||||||
| chr2:231137556 | T | A | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1884-1180T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137556 | |||||||
| chr2:231137721 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884-1015A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231137721 | |||||||
| chr2:231138345 | G | A | 2 | a0001c0001t0001g0328 a0001c0001t0001g0330 |
2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1884-391G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138345 | |||||||
| chr2:231138389 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1884-347T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138389 | |||||||
| chr2:231138475 | C | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
4 | HG01074.hp1 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884-261C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138475 | |||||||
| chr2:231138675 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1884-61T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138675 | |||||||
| chr2:231138703 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1884-33A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 16/24 | chr2 | 231138703 | |||||||
| chr2:231139004 | C | T | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1998+154C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139004 | |||||||
| chr2:231139038 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1998+188A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139038 | |||||||
| chr2:231139118 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1998+268G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139118 | |||||||
| chr2:231139123 | T | C | 2 | a0001c0001t0003g0004 a0001c0001t0003g0122 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1998+273T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139123 | |||||||
| chr2:231139124 | G | GT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0238 a0001c0001t0001g0251 others(4): Show |
7 | HG01952.hp1 HG03225.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.1998+282dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139124 | ||||||
| chr2:231139166 | CTT | C | 4 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0167 others(1): Show |
4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998+318_1998+319d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139166 | ||||||
| chr2:231139250 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1998+400C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139250 | |||||||
| chr2:231139291 | A | G | 1 | a0001c0001t0002g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1998+441A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139291 | |||||||
| chr2:231139314 | C | CT | 8 | a0001c0001t0002g0035 a0001c0001t0002g0039 a0001c0001t0002g0060 others(5): Show |
8 | HG01074.hp1 HG01123.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1998+487dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | ||||||
| chr2:231139314 | CT | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
184 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1998+487delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | ||||||
| chr2:231139314 | CTT | C | 54 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(51): Show |
56 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1998+486_1998+487d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | ||||||
| chr2:231139314 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1998+477_1998+487d others(13): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139314 | ||||||
| chr2:231139320 | T | C | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
9 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1998+470T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139320 | |||||||
| chr2:231139558 | T | TA | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
184 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1998+725dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139558 | ||||||
| chr2:231139558 | T | TAA | 44 | a0001c0001t0001g0087 a0001c0001t0001g0179 a0001c0001t0001g0233 others(41): Show |
46 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1998+724_1998+725d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231139558 | ||||||
| chr2:231139573 | A | AG | 3 | a0001c0002t0004g0027 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03130.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1998+723_1998+724i others(3): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139573 | |||||||
| chr2:231139576 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1998+726G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139576 | |||||||
| chr2:231139579 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0003g0129 |
2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1998+729G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139579 | |||||||
| chr2:231139755 | G | A | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1998+905G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139755 | |||||||
| chr2:231139829 | T | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1998+979T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231139829 | |||||||
| chr2:231140220 | G | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1998+1370G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140220 | |||||||
| chr2:231140357 | A | G | 1 | a0001c0002t0004g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1998+1507A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140357 | |||||||
| chr2:231140390 | G | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1998+1540G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140390 | |||||||
| chr2:231140406 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1998+1556G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140406 | |||||||
| chr2:231140495 | C | CA | 17 | a0001c0001t0001g0131 a0001c0001t0001g0185 a0001c0001t0001g0196 others(14): Show |
17 | HG01928.hp1 HG01981.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1998+1665dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231140495 | ||||||
| chr2:231140495 | CA | C | 12 | a0001c0001t0001g0177 a0001c0001t0001g0200 a0001c0001t0001g0237 others(9): Show |
12 | HG01070.hp2 HG01516.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1998+1665delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231140495 | ||||||
| chr2:231140786 | G | C | 1 | a0001c0001t0002g0042 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1998+1936G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231140786 | |||||||
| chr2:231141035 | C | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 |
3 | HG02027.hp1 NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1998+2185C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141035 | |||||||
| chr2:231141305 | G | GA | 9 | a0001c0001t0001g0200 a0001c0001t0001g0269 a0001c0001t0001g0292 others(6): Show |
9 | HG01981.hp1 HG02015.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1998+2469dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141305 | ||||||
| chr2:231141305 | GA | G | 6 | a0001c0001t0001g0025 a0001c0001t0002g0057 a0001c0001t0002g0074 others(3): Show |
6 | HG01168.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1998+2469delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141305 | ||||||
| chr2:231141395 | C | T | 58 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(55): Show |
61 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1998+2545C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141395 | |||||||
| chr2:231141412 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1998+2562C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141412 | |||||||
| chr2:231141420 | ACT | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0267 others(1): Show |
4 | HG01928.hp1 HG02300.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998+2571_1998+257 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141420 | |||||||
| chr2:231141420 | ACTT | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(72): Show |
77 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1998+2571_1998+257 others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141420 | |||||||
| chr2:231141421 | C | CT | 15 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0214 others(12): Show |
15 | HG02280.hp1 HG02738.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.1998+2590dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141421 | ||||||
| chr2:231141421 | CT | C | 12 | a0001c0001t0002g0077 a0001c0001t0002g0086 a0001c0001t0003g0118 others(9): Show |
12 | HG01168.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1998+2590delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141421 | ||||||
| chr2:231141496 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1998+2646G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141496 | |||||||
| chr2:231141568 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1998+2718C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141568 | |||||||
| chr2:231141583 | AT | A | 7 | a0001c0001t0002g0014 a0001c0001t0002g0101 a0001c0002t0004g0026 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1998+2748delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231141583 | ||||||
| chr2:231141737 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1998+2887G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231141737 | |||||||
| chr2:231142043 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1998+3193C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142043 | |||||||
| chr2:231142044 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1998+3194G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142044 | |||||||
| chr2:231142072 | G | A | 48 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1998+3222G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142072 | |||||||
| chr2:231142208 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1998+3358C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142208 | |||||||
| chr2:231142510 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1998+3660C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142510 | |||||||
| chr2:231142541 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998+3691G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142541 | |||||||
| chr2:231142568 | C | A | 2 | a0001c0001t0003g0118 a0001c0001t0003g0119 |
2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1999-3672C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142568 | |||||||
| chr2:231142636 | T | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(33): Show |
38 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1999-3604T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142636 | |||||||
| chr2:231142713 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1999-3527C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142713 | |||||||
| chr2:231142865 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1999-3375T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231142865 | |||||||
| chr2:231143065 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(79): Show |
84 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1999-3175T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143065 | |||||||
| chr2:231143140 | A | AT | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1999-3090dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143140 | ||||||
| chr2:231143140 | A | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1999-3100A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143140 | |||||||
| chr2:231143187 | G | GGGTTT | 5 | a0001c0001t0001g0176 a0001c0001t0001g0188 a0001c0001t0001g0194 others(2): Show |
5 | HG02886.hp1 HG03579.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999-2997_1999-299 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | ||||||
| chr2:231143187 | GGGTTT | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
140 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1999-2997_1999-299 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | ||||||
| chr2:231143187 | GGGTTTGG others(3): Show |
G | 41 | a0001c0001t0001g0025 a0001c0001t0001g0249 a0001c0001t0001g0250 others(38): Show |
43 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.1999-3002_1999-299 others(14): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | ||||||
| chr2:231143187 | GGGTTTGG others(8): Show |
G | 115 | a0001c0001t0001g0011 a0001c0001t0001g0201 a0001c0001t0001g0207 others(112): Show |
118 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1999-3007_1999-299 others(19): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | ||||||
| chr2:231143187 | GGGTTTGG others(13): Show |
G | 7 | a0001c0001t0002g0037 a0001c0001t0002g0069 a0001c0001t0002g0096 others(4): Show |
7 | HG00733.hp1 HG03017.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1999-3012_1999-299 others(24): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231143187 | ||||||
| chr2:231143244 | G | C | 2 | a0001c0001t0002g0070 a0001c0001t0002g0342 |
2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1999-2996G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143244 | |||||||
| chr2:231143337 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-2903C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143337 | |||||||
| chr2:231143339 | C | G | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1999-2901C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143339 | |||||||
| chr2:231143441 | G | A | 4 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0167 others(1): Show |
4 | HG02622.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999-2799G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143441 | |||||||
| chr2:231143591 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1999-2649C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143591 | |||||||
| chr2:231143620 | T | C | 1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1999-2620T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143620 | |||||||
| chr2:231143674 | G | C | 1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1999-2566G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143674 | |||||||
| chr2:231143725 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1999-2515A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143725 | |||||||
| chr2:231143759 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1999-2481A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143759 | |||||||
| chr2:231143836 | A | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG03927.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1999-2404A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143836 | |||||||
| chr2:231143945 | T | C | 1 | a0001c0006t0002g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1999-2295T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231143945 | |||||||
| chr2:231144130 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-2110G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144130 | |||||||
| chr2:231144159 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1999-2081G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144159 | |||||||
| chr2:231144211 | C | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(88): Show |
93 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1999-2029C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144211 | |||||||
| chr2:231144252 | C | CT | 6 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0049 others(3): Show |
6 | NA18968.hp1 NA18972.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-1973dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144252 | ||||||
| chr2:231144333 | C | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1999-1907C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144333 | |||||||
| chr2:231144336 | C | T | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1999-1904C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144336 | |||||||
| chr2:231144356 | A | T | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1999-1884A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144356 | |||||||
| chr2:231144401 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1999-1839G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144401 | |||||||
| chr2:231144418 | A | AT | 29 | a0001c0001t0001g0024 a0001c0001t0002g0013 a0001c0001t0002g0014 others(26): Show |
29 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1999-1790dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | AT | A | 6 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0056 others(3): Show |
6 | HG00323.hp1 HG01169.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-1790delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | ATTT | A | 26 | a0001c0001t0001g0199 a0001c0001t0001g0206 a0001c0001t0001g0211 others(23): Show |
26 | HG00438.hp1 HG00544.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1999-1792_1999-179 others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | ATTTT | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
90 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1999-1793_1999-179 others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | ATTTTT | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0087 others(115): Show |
122 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999-1794_1999-179 others(9): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | ATTTTTT | A | 12 | a0001c0001t0001g0207 a0001c0001t0001g0229 a0001c0001t0001g0250 others(9): Show |
12 | HG01070.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1999-1795_1999-179 others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | ATTTTTTT others(4): Show |
A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1999-1800_1999-179 others(15): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0041 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1999-1801_1999-179 others(16): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144418 | ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG01074.hp1 HG04204.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1999-1802_1999-179 others(17): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231144418 | ||||||
| chr2:231144423 | T | A | 1 | a0001c0001t0002g0068 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1999-1817T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144423 | |||||||
| chr2:231144498 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1999-1742C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144498 | |||||||
| chr2:231144648 | A | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1999-1592A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144648 | |||||||
| chr2:231144662 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | NA19065.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1999-1578C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144662 | |||||||
| chr2:231144757 | G | T | 1 | a0001c0001t0002g0038 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1999-1483G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144757 | |||||||
| chr2:231144812 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1999-1428A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231144812 | |||||||
| chr2:231145220 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1999-1020T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145220 | |||||||
| chr2:231145463 | A | G | 1 | a0001c0001t0005g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1999-777A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145463 | |||||||
| chr2:231145660 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0099 |
2 | NA18973.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1999-580G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145660 | |||||||
| chr2:231145681 | G | C | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1999-559G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145681 | |||||||
| chr2:231145749 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-491C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145749 | |||||||
| chr2:231145756 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1999-484G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145756 | |||||||
| chr2:231145869 | G | A | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1999-371G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145869 | |||||||
| chr2:231145894 | C | CA | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0169 others(41): Show |
46 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1999-318dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | ||||||
| chr2:231145894 | C | CAA | 14 | a0001c0001t0001g0282 a0001c0001t0001g0300 a0001c0001t0002g0076 others(11): Show |
14 | HG01361.hp1 HG01943.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1999-319_1999-318d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | ||||||
| chr2:231145894 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(102): Show |
109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1999-318delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | ||||||
| chr2:231145894 | CAA | C | 9 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0001g0262 others(6): Show |
9 | HG01168.hp1 HG01891.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-319_1999-318d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | ||||||
| chr2:231145894 | CAAAAAAA others(2): Show |
C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1999-326_1999-318d others(11): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | ||||||
| chr2:231145894 | CAAAAAAA others(4): Show |
C | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1999-328_1999-318d others(13): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231145894 | ||||||
| chr2:231145966 | G | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(77): Show |
82 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1999-274G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 17/24 | chr2 | 231145966 | |||||||
| chr2:231146404 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2115+48C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146404 | |||||||
| chr2:231146463 | A | T | 1 | a0001c0001t0002g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2115+107A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146463 | |||||||
| chr2:231146547 | T | TAC | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2115+192_2115+193i others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231146547 | ||||||
| chr2:231146726 | C | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.2115+370C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146726 | |||||||
| chr2:231146842 | G | T | 1 | a0001c0001t0003g0140 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2115+486G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231146842 | |||||||
| chr2:231147103 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2115+747C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147103 | |||||||
| chr2:231147124 | C | G | 1 | a0001c0001t0003g0139 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2115+768C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147124 | |||||||
| chr2:231147252 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0295 |
3 | HG00423.hp1 HG00673.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2115+896G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147252 | |||||||
| chr2:231147313 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2115+957G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147313 | |||||||
| chr2:231147661 | T | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(76): Show |
81 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.2115+1305T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147661 | |||||||
| chr2:231147670 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2115+1314G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147670 | |||||||
| chr2:231147675 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2115+1319G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147675 | |||||||
| chr2:231147741 | T | G | 1 | a0001c0001t0002g0033 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2115+1385T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231147741 | |||||||
| chr2:231148273 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2115+1917A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148273 | |||||||
| chr2:231148590 | G | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.2115+2234G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148590 | |||||||
| chr2:231148592 | A | C | 1 | a0001c0001t0002g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2115+2236A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148592 | |||||||
| chr2:231148636 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0177 a0001c0001t0001g0178 |
4 | NA18940.hp1 NA18973.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2115+2280A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148636 | |||||||
| chr2:231148935 | A | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2115+2579A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231148935 | |||||||
| chr2:231149073 | G | A | 2 | a0001c0001t0003g0145 a0001c0001t0003g0146 |
2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2115+2717G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149073 | |||||||
| chr2:231149339 | A | C | 1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2115+2983A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149339 | |||||||
| chr2:231149425 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2115+3069G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149425 | |||||||
| chr2:231149480 | CA | C | 6 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
6 | NA18942.hp1 NA18980.hp2 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.2115+3131delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231149480 | ||||||
| chr2:231149482 | A | G | 14 | a0001c0001t0001g0204 a0001c0001t0001g0235 a0001c0001t0001g0236 others(11): Show |
15 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.2115+3126A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149482 | |||||||
| chr2:231149608 | C | T | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2115+3252C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149608 | |||||||
| chr2:231149717 | C | T | 4 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0003g0334 others(1): Show |
4 | HG02145.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2115+3361C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149717 | |||||||
| chr2:231149726 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2115+3370A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231149726 | |||||||
| chr2:231150084 | G | A | 7 | a0001c0001t0001g0169 a0001c0001t0001g0233 a0001c0001t0001g0292 others(4): Show |
7 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2116-3480G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150084 | |||||||
| chr2:231150129 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2116-3435C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150129 | |||||||
| chr2:231150189 | C | CA | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-3367dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231150189 | ||||||
| chr2:231150260 | T | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | NA18979.hp2 NA18988.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2116-3304T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150260 | |||||||
| chr2:231150344 | CAAG | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2116-3219_2116-321 others(7): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150344 | |||||||
| chr2:231150423 | T | G | 6 | a0001c0001t0002g0088 a0001c0002t0004g0026 a0001c0002t0004g0027 others(3): Show |
6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2116-3141T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150423 | |||||||
| chr2:231150659 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2116-2905A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150659 | |||||||
| chr2:231150703 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2116-2861C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150703 | |||||||
| chr2:231150892 | C | T | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2116-2672C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150892 | |||||||
| chr2:231150920 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2116-2644C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231150920 | |||||||
| chr2:231151009 | G | A | 5 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(2): Show |
5 | NA18966.hp1 NA19063.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-2555G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151009 | |||||||
| chr2:231151545 | T | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2116-2019T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151545 | |||||||
| chr2:231151585 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2116-1979C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151585 | |||||||
| chr2:231151641 | C | CT | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2116-1920dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151641 | ||||||
| chr2:231151801 | GA | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0171 others(19): Show |
24 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.2116-1761delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151801 | ||||||
| chr2:231151803 | A | AT | 28 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0001g0226 others(25): Show |
28 | HG00438.hp1 HG00673.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2116-1735dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151803 | ||||||
| chr2:231151803 | A | T | 9 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0175 others(6): Show |
9 | HG00673.hp1 HG01361.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.2116-1761A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151803 | |||||||
| chr2:231151803 | AT | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0087 others(103): Show |
110 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2116-1735delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151803 | ||||||
| chr2:231151803 | ATT | A | 15 | a0001c0001t0001g0282 a0001c0001t0003g0120 a0001c0001t0003g0123 others(12): Show |
15 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2116-1736_2116-173 others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231151803 | ||||||
| chr2:231151831 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2116-1733A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231151831 | |||||||
| chr2:231152427 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2116-1137G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152427 | |||||||
| chr2:231152461 | C | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-1103C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152461 | |||||||
| chr2:231152588 | C | G | 1 | a0001c0001t0001g0010 | 2 | HG00735.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2116-976C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152588 | |||||||
| chr2:231152627 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-937A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231152627 | |||||||
| chr2:231153032 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2116-532G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153032 | |||||||
| chr2:231153169 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-395A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153169 | |||||||
| chr2:231153170 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-394G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153170 | |||||||
| chr2:231153171 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-393G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153171 | |||||||
| chr2:231153193 | G | A | 2 | a0001c0001t0002g0013 a0004c0004t0002g0012 |
2 | NA19003.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2116-371G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153193 | |||||||
| chr2:231153540 | T | C | 1 | a0002c0003t0003g0156 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2116-24T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153540 | |||||||
| chr2:231153543 | T | G | 1 | a0002c0003t0003g0156 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2116-21T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153543 | |||||||
| chr2:231153544 | T | A | 1 | a0002c0003t0003g0156 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2116-20T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 18/24 | chr2 | 231153544 | |||||||
| chr2:231153794 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+128C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231153794 | |||||||
| chr2:231153911 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2218+245C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231153911 | |||||||
| chr2:231154003 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2218+337C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154003 | |||||||
| chr2:231154070 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2218+404G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154070 | |||||||
| chr2:231154074 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2218+408T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154074 | |||||||
| chr2:231154087 | G | A | 1 | a0001c0002t0004g0030 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2218+421G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154087 | |||||||
| chr2:231154105 | C | T | 6 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(3): Show |
6 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.2218+439C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154105 | |||||||
| chr2:231154128 | C | A | 8 | a0001c0001t0001g0025 a0001c0001t0002g0078 a0001c0002t0004g0026 others(5): Show |
8 | HG01516.hp1 HG02280.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2218+462C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154128 | |||||||
| chr2:231154265 | C | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
243 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.2218+599C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154265 | |||||||
| chr2:231154375 | A | T | 1 | a0001c0001t0001g0255 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2218+709A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154375 | |||||||
| chr2:231154455 | CTGTT | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2218+790_2218+793d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154455 | |||||||
| chr2:231154575 | A | C | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2218+909A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154575 | |||||||
| chr2:231154655 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+989G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231154655 | |||||||
| chr2:231155048 | G | A | 2 | a0001c0002t0004g0027 a0001c0002t0004g0028 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2218+1382G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155048 | |||||||
| chr2:231155074 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2218+1408A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155074 | |||||||
| chr2:231155203 | G | A | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2218+1537G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155203 | |||||||
| chr2:231155507 | TA | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2218+1850delA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231155507 | ||||||
| chr2:231155523 | T | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2218+1857T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155523 | |||||||
| chr2:231155587 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2218+1921G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155587 | |||||||
| chr2:231155627 | T | TA | 11 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(8): Show |
11 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2218+1962dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231155627 | ||||||
| chr2:231155741 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+2075G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155741 | |||||||
| chr2:231155887 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2218+2221G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231155887 | |||||||
| chr2:231156107 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2218+2441T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156107 | |||||||
| chr2:231156393 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2218+2727T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156393 | |||||||
| chr2:231156430 | A | G | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2218+2764A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156430 | |||||||
| chr2:231156479 | A | T | 2 | a0001c0001t0001g0252 a0001c0001t0003g0167 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2218+2813A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156479 | |||||||
| chr2:231156497 | A | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(21): Show |
26 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2218+2831A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156497 | |||||||
| chr2:231156547 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2218+2881T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156547 | |||||||
| chr2:231156548 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
240 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2218+2882G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156548 | |||||||
| chr2:231156588 | T | C | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2218+2922T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156588 | |||||||
| chr2:231156597 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2218+2931T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156597 | |||||||
| chr2:231156640 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0001g0327 others(3): Show |
7 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2218+2974T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156640 | |||||||
| chr2:231156700 | A | G | 7 | a0001c0001t0003g0142 a0001c0001t0003g0150 a0001c0001t0003g0151 others(4): Show |
7 | NA18972.hp1 NA18975.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2218+3034A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156700 | |||||||
| chr2:231156725 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2218+3059T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156725 | |||||||
| chr2:231156924 | T | C | 1 | a0002c0003t0002g0081 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2218+3258T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231156924 | |||||||
| chr2:231157253 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2218+3587G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157253 | |||||||
| chr2:231157430 | C | CT | 9 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0001g0327 others(6): Show |
10 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2218+3779dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231157430 | ||||||
| chr2:231157434 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2218+3768T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157434 | |||||||
| chr2:231157441 | T | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2218+3775T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157441 | |||||||
| chr2:231157442 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(28): Show |
33 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.2218+3776T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157442 | |||||||
| chr2:231157586 | T | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-3754T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157586 | |||||||
| chr2:231157586 | T | TG | 84 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(81): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2219-3746dupG | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231157586 | ||||||
| chr2:231157693 | T | G | 41 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(38): Show |
41 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.2219-3647T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157693 | |||||||
| chr2:231157694 | G | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2219-3646G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157694 | |||||||
| chr2:231157976 | G | C | 1 | a0001c0001t0002g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2219-3364G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231157976 | |||||||
| chr2:231158218 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(27): Show |
32 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.2219-3122C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158218 | |||||||
| chr2:231158246 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-3094G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158246 | |||||||
| chr2:231158267 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.2219-3073G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158267 | |||||||
| chr2:231158316 | A | C | 1 | a0001c0001t0001g0303 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2219-3024A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158316 | |||||||
| chr2:231158319 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2219-3021A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158319 | |||||||
| chr2:231158569 | A | G | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2219-2771A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158569 | |||||||
| chr2:231158609 | T | C | 11 | a0001c0001t0001g0234 a0001c0001t0003g0118 a0001c0001t0003g0119 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2219-2731T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158609 | |||||||
| chr2:231158781 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2219-2559G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158781 | |||||||
| chr2:231158857 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2219-2483G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158857 | |||||||
| chr2:231158961 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2219-2379T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231158961 | |||||||
| chr2:231159281 | G | A | 2 | a0001c0001t0003g0145 a0001c0001t0003g0146 |
2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2219-2059G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159281 | |||||||
| chr2:231159285 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2219-2055G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159285 | |||||||
| chr2:231159499 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2219-1841A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159499 | |||||||
| chr2:231159823 | G | T | 1 | a0001c0001t0002g0021 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2219-1517G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159823 | |||||||
| chr2:231159845 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2219-1495T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159845 | |||||||
| chr2:231159923 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2219-1417G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159923 | |||||||
| chr2:231159993 | C | T | 2 | a0001c0002t0004g0026 a0001c0002t0004g0030 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2219-1347C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231159993 | |||||||
| chr2:231160174 | A | G | 1 | a0001c0001t0003g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2219-1166A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160174 | |||||||
| chr2:231160185 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2219-1155A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160185 | |||||||
| chr2:231160308 | A | C | 1 | a0001c0001t0003g0352 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2219-1032A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160308 | |||||||
| chr2:231160387 | G | C | 1 | a0001c0001t0001g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2219-953G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160387 | |||||||
| chr2:231160570 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
310 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.2219-770G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160570 | |||||||
| chr2:231160608 | C | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-732C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160608 | |||||||
| chr2:231160919 | T | C | 2 | a0001c0001t0002g0070 a0001c0001t0002g0342 |
2 | NA18942.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2219-421T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160919 | |||||||
| chr2:231160960 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2219-380C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231160960 | |||||||
| chr2:231161001 | A | G | 1 | a0001c0001t0003g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2219-339A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161001 | |||||||
| chr2:231161018 | C | G | 1 | a0001c0001t0003g0352 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2219-322C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161018 | |||||||
| chr2:231161105 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0222 a0001c0001t0001g0227 |
3 | NA18947.hp2 NA18950.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.2219-235G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161105 | |||||||
| chr2:231161166 | C | T | 32 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0170 others(29): Show |
34 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.2219-174C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161166 | |||||||
| chr2:231161177 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2219-163A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161177 | |||||||
| chr2:231161238 | T | TA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(83): Show |
90 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.2219-88dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231161238 | ||||||
| chr2:231161280 | G | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(39): Show |
44 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2219-60G>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161280 | |||||||
| chr2:231161336 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0096 |
2 | HG00733.hp1 NA20905.hp2 |
splice_region_variant&intron_variant | LOW | c.2219-4A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 19/24 | chr2 | 231161336 | |||||||
| chr2:231161524 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2388+15C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231161524 | |||||||
| chr2:231161552 | C | T | 2 | a0001c0001t0001g0328 a0001c0001t0001g0330 |
2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2388+43C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231161552 | |||||||
| chr2:231161553 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2388+44G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231161553 | |||||||
| chr2:231162042 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2388+533C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162042 | |||||||
| chr2:231162582 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-1053G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162582 | |||||||
| chr2:231162599 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-1036G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162599 | |||||||
| chr2:231162826 | C | CA | 13 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(10): Show |
13 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2389-795dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231162826 | ||||||
| chr2:231162854 | A | G | 2 | a0001c0001t0002g0083 a0001c0001t0002g0101 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2389-781A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162854 | |||||||
| chr2:231162862 | C | A | 7 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2389-773C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231162862 | |||||||
| chr2:231163016 | C | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-619C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163016 | |||||||
| chr2:231163029 | G | A | 1 | a0001c0002t0004g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2389-606G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163029 | |||||||
| chr2:231163056 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-579G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163056 | |||||||
| chr2:231163080 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-555A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163080 | |||||||
| chr2:231163100 | C | CA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(86): Show |
93 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2389-521dupA | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231163100 | ||||||
| chr2:231163118 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2389-517A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163118 | |||||||
| chr2:231163190 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0179 a0001c0001t0001g0180 others(8): Show |
12 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.2389-445C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163190 | |||||||
| chr2:231163207 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2389-428C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163207 | |||||||
| chr2:231163292 | G | T | 1 | a0001c0001t0001g0339 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2389-343G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 20/24 | chr2 | 231163292 | |||||||
| chr2:231163865 | A | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+138A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231163865 | |||||||
| chr2:231163870 | A | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+143A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231163870 | |||||||
| chr2:231163986 | A | G | 10 | a0001c0001t0003g0118 a0001c0001t0003g0119 a0001c0001t0003g0123 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2481+259A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231163986 | |||||||
| chr2:231164031 | T | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2481+304T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164031 | |||||||
| chr2:231164055 | A | G | 11 | a0001c0001t0002g0066 a0001c0001t0003g0118 a0001c0001t0003g0119 others(8): Show |
11 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2481+328A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164055 | |||||||
| chr2:231164086 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2481+359G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164086 | |||||||
| chr2:231164441 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2481+714A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164441 | |||||||
| chr2:231164484 | C | CATG | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-714_2482-713i others(5): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231164484 | ||||||
| chr2:231164579 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2482-621T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164579 | |||||||
| chr2:231164589 | A | G | 5 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(2): Show |
5 | HG00438.hp2 HG02027.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-611A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164589 | |||||||
| chr2:231164716 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2482-484G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164716 | |||||||
| chr2:231164783 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-417G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164783 | |||||||
| chr2:231164784 | C | T | 1 | a0001c0001t0002g0342 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2482-416C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164784 | |||||||
| chr2:231164854 | A | G | 48 | a0001c0001t0001g0249 a0001c0001t0001g0282 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2482-346A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164854 | |||||||
| chr2:231164885 | C | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2482-315C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164885 | |||||||
| chr2:231164890 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-310G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231164890 | |||||||
| chr2:231165021 | GATTTATA others(3): Show |
G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0169 others(1): Show |
6 | HG02027.hp2 HG03195.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-166_2482-157d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165021 | ||||||
| chr2:231165023 | TTTATATA others(28): Show |
T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0285 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2482-175_2482-141d others(37): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165023 | ||||||
| chr2:231165024 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2482-176T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165024 | |||||||
| chr2:231165024 | T | TTA | 3 | a0001c0001t0001g0213 a0001c0001t0001g0298 a0001c0001t0001g0320 |
3 | HG02683.hp2 NA18952.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2482-168_2482-167d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | T | TTATA | 3 | a0001c0001t0001g0174 a0001c0001t0001g0192 a0001c0001t0003g0341 |
3 | HG02965.hp2 NA18968.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2482-170_2482-167d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(5): Show |
T | 4 | a0001c0001t0001g0322 a0001c0001t0003g0123 a0001c0001t0003g0124 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-166_2482-155d others(14): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(7): Show |
T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0233 a0001c0001t0001g0293 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-166_2482-153d others(16): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0223 a0001c0001t0003g0118 a0001c0001t0003g0119 others(1): Show |
4 | HG03209.hp1 HG03540.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-166_2482-151d others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(11): Show |
T | 1 | a0001c0001t0001g0331 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2482-166_2482-149d others(20): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(13): Show |
T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0018 |
2 | NA19062.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2482-166_2482-147d others(22): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(15): Show |
T | 1 | a0001c0001t0001g0305 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2482-166_2482-145d others(24): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(17): Show |
T | 1 | a0001c0001t0001g0319 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2482-166_2482-143d others(26): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(19): Show |
T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0181 a0001c0001t0001g0183 others(4): Show |
7 | HG00408.hp1 HG00673.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.2482-166_2482-141d others(28): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(21): Show |
T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0226 a0001c0001t0001g0295 others(5): Show |
8 | HG00423.hp1 HG00673.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-166_2482-139d others(30): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(23): Show |
T | 1 | a0001c0001t0001g0010 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2482-166_2482-137d others(32): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(25): Show |
T | 16 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
16 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.2482-166_2482-135d others(34): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(27): Show |
T | 6 | a0001c0001t0001g0251 a0001c0001t0001g0265 a0001c0001t0001g0288 others(3): Show |
6 | HG01109.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-166_2482-133d others(36): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(29): Show |
T | 15 | a0001c0001t0001g0230 a0001c0001t0001g0240 a0001c0001t0001g0241 others(12): Show |
15 | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2482-166_2482-131d others(38): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(31): Show |
T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(62): Show |
67 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.2482-166_2482-129d others(40): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(35): Show |
T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0176 a0001c0001t0001g0313 |
3 | HG03710.hp2 NA18942.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2482-166_2482-125d others(44): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(37): Show |
T | 6 | a0001c0001t0001g0024 a0001c0002t0004g0026 a0001c0002t0004g0027 others(3): Show |
6 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-166_2482-123d others(46): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(45): Show |
T | 5 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-166_2482-115d others(54): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165024 | TTATATAT others(47): Show |
T | 48 | a0001c0001t0001g0249 a0001c0001t0001g0282 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2482-166_2482-113d others(56): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165024 | ||||||
| chr2:231165026 | ATATATAT others(1): Show |
A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0215 others(5): Show |
9 | HG01981.hp1 HG02129.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-166_2482-159d others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165026 | ||||||
| chr2:231165028 | A | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | NA18947.hp2 NA18971.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-172A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165028 | |||||||
| chr2:231165028 | ATATATT | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0304 |
3 | HG02056.hp1 NA18975.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2482-166_2482-161d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165028 | ||||||
| chr2:231165030 | ATATT | A | 8 | a0001c0001t0001g0170 a0001c0001t0001g0188 a0001c0001t0001g0190 others(5): Show |
8 | HG02451.hp2 HG03579.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2482-166_2482-163d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165030 | ||||||
| chr2:231165032 | ATT | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0212 a0001c0001t0001g0217 others(5): Show |
8 | HG01123.hp1 HG03927.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-166_2482-165d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165032 | ||||||
| chr2:231165034 | T | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0171 others(23): Show |
27 | HG00609.hp1 HG00639.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2482-166T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165034 | |||||||
| chr2:231165034 | T | TTA | 9 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0036 others(6): Show |
9 | HG02523.hp2 HG03942.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.2482-110_2482-109d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | T | TTATA | 8 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0046 others(5): Show |
8 | HG02109.hp1 HG04228.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-112_2482-109d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | T | TTATATA | 4 | a0001c0001t0002g0016 a0001c0001t0002g0066 a0001c0001t0002g0078 others(1): Show |
4 | HG01081.hp1 HG01516.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-114_2482-109d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | T | TTATATAT others(3): Show |
1 | a0001c0001t0002g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2482-118_2482-109d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTA | T | 14 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0039 others(11): Show |
14 | HG01074.hp1 HG01515.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.2482-110_2482-109d others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATA | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0038 a0001c0001t0002g0047 others(11): Show |
14 | HG00438.hp2 HG00639.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2482-112_2482-109d others(6): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATA | T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0037 a0001c0001t0002g0043 others(12): Show |
16 | HG00323.hp1 HG00609.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2482-114_2482-109d others(8): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATAT others(1): Show |
T | 3 | a0001c0001t0002g0060 a0001c0001t0002g0077 a0001c0001t0002g0108 |
3 | HG01168.hp2 HG01884.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.2482-116_2482-109d others(10): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATAT others(3): Show |
T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0069 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2482-118_2482-109d others(12): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATAT others(9): Show |
T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0067 a0001c0001t0002g0095 others(1): Show |
4 | HG01981.hp2 HG02300.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-124_2482-109d others(18): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATAT others(13): Show |
T | 1 | a0001c0001t0002g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2482-128_2482-109d others(22): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0002g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2482-134_2482-109d others(28): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATAT others(23): Show |
T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0101 |
3 | HG01243.hp2 NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2482-138_2482-109d others(32): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165034 | TTATATAT others(33): Show |
T | 1 | a0001c0001t0002g0114 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2482-148_2482-109d others(42): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231165034 | ||||||
| chr2:231165036 | A | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0092 |
2 | HG00735.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2482-164A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165036 | |||||||
| chr2:231165038 | A | T | 2 | a0001c0001t0001g0322 a0001c0001t0002g0107 |
2 | NA18957.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2482-162A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165038 | |||||||
| chr2:231165040 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2482-160A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165040 | |||||||
| chr2:231165042 | A | T | 2 | a0001c0001t0001g0221 a0001c0001t0002g0043 |
2 | HG00323.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2482-158A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165042 | |||||||
| chr2:231165044 | A | T | 2 | a0001c0001t0001g0223 a0001c0001t0002g0077 |
2 | HG01168.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2482-156A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165044 | |||||||
| chr2:231165048 | A | ACAATATA others(19): Show |
1 | a0001c0001t0002g0103 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-152_2482-151i others(28): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165048 | |||||||
| chr2:231165052 | A | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0104 |
2 | HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2482-148A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165052 | |||||||
| chr2:231165056 | A | T | 1 | a0001c0001t0002g0103 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-144A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165056 | |||||||
| chr2:231165063 | T | C | 2 | a0001c0001t0002g0103 a0001c0001t0002g0106 |
2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2482-137T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165063 | |||||||
| chr2:231165070 | A | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-130A>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165070 | |||||||
| chr2:231165071 | T | C | 1 | a0001c0001t0002g0103 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-129T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165071 | |||||||
| chr2:231165079 | T | C | 1 | a0001c0001t0002g0103 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2482-121T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165079 | |||||||
| chr2:231165082 | A | G | 4 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482-118A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165082 | |||||||
| chr2:231165088 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0096 |
2 | HG00733.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2482-112A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165088 | |||||||
| chr2:231165191 | T | C | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-9T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 21/24 | chr2 | 231165191 | |||||||
| chr2:231165448 | C | CTA | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2568+162_2568+163i others(4): Show |
PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165448 | |||||||
| chr2:231165587 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2569-284C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165587 | |||||||
| chr2:231165796 | C | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.2569-75C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165796 | |||||||
| chr2:231165841 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2569-30G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 22/24 | chr2 | 231165841 | |||||||
| chr2:231166147 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
242 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.2715+130A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166147 | |||||||
| chr2:231166176 | A | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0290 |
2 | NA19076.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2715+159A>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166176 | |||||||
| chr2:231166503 | G | A | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2715+486G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166503 | |||||||
| chr2:231166508 | C | CT | 226 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
236 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.2715+503dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231166508 | ||||||
| chr2:231166642 | G | A | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+625G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166642 | |||||||
| chr2:231166691 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+674C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166691 | |||||||
| chr2:231166886 | C | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+869C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231166886 | |||||||
| chr2:231167020 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2715+1003T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167020 | |||||||
| chr2:231167134 | G | A | 5 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+1117G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167134 | |||||||
| chr2:231167387 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2715+1370G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167387 | |||||||
| chr2:231167491 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2715+1474T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231167491 | |||||||
| chr2:231168134 | C | T | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2715+2117C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168134 | |||||||
| chr2:231168150 | C | G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02258.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2715+2133C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168150 | |||||||
| chr2:231168307 | T | G | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2716-2259T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168307 | |||||||
| chr2:231168361 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG01243.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2716-2205G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168361 | |||||||
| chr2:231168578 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2716-1988T>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168578 | |||||||
| chr2:231168615 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2716-1951G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168615 | |||||||
| chr2:231168688 | T | C | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2716-1878T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168688 | |||||||
| chr2:231168760 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2716-1806A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168760 | |||||||
| chr2:231168836 | G | T | 1 | a0001c0001t0006g0279 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2716-1730G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231168836 | |||||||
| chr2:231169060 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2716-1506T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169060 | |||||||
| chr2:231169087 | A | AC | 73 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2716-1477dupC | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231169087 | ||||||
| chr2:231169159 | T | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0231 a0001c0001t0001g0232 others(8): Show |
11 | HG02080.hp1 HG02738.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.2716-1407T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169159 | |||||||
| chr2:231169563 | T | C | 2 | a0001c0001t0001g0025 a0001c0005t0001g0031 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2716-1003T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169563 | |||||||
| chr2:231169628 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.2716-938C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 23/24 | chr2 | 231169628 | |||||||
| chr2:231170801 | G | A | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*9+80G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231170801 | |||||||
| chr2:231170820 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.*9+99T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231170820 | |||||||
| chr2:231170929 | C | G | 5 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.*9+208C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231170929 | |||||||
| chr2:231171013 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.*9+292C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171013 | |||||||
| chr2:231171079 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.*9+358C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171079 | |||||||
| chr2:231171138 | C | G | 2 | a0001c0001t0003g0118 a0001c0001t0003g0119 |
2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.*9+417C>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171138 | |||||||
| chr2:231171549 | A | AT | 90 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.*9+851dupT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr2 | 231171549 | ||||||
| chr2:231171549 | A | ATT | 15 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0169 others(12): Show |
16 | HG00558.hp1 HG02027.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.*9+850_*9+851dupTT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr2 | 231171549 | ||||||
| chr2:231171549 | AT | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(31): Show |
36 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.*9+851delT | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr2 | 231171549 | ||||||
| chr2:231171634 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*10-901G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171634 | |||||||
| chr2:231171660 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*10-875G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171660 | |||||||
| chr2:231171682 | G | A | 48 | a0001c0001t0001g0249 a0001c0001t0001g0282 a0001c0001t0003g0004 others(45): Show |
50 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.*10-853G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171682 | |||||||
| chr2:231171808 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*10-727G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171808 | |||||||
| chr2:231171853 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG01074.hp1 HG04204.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.*10-682G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171853 | |||||||
| chr2:231171869 | C | A | 2 | a0001c0001t0003g0166 a0001c0001t0003g0167 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*10-666C>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171869 | |||||||
| chr2:231171947 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*10-588C>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231171947 | |||||||
| chr2:231172129 | T | G | 43 | a0001c0001t0001g0249 a0001c0001t0001g0282 a0001c0001t0003g0004 others(40): Show |
45 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.*10-406T>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172129 | |||||||
| chr2:231172169 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0131 others(79): Show |
84 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.*10-366G>A | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172169 | |||||||
| chr2:231172242 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*10-293A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172242 | |||||||
| chr2:231172280 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.*10-255A>G | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172280 | |||||||
| chr2:231172315 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.*10-220G>T | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172315 | |||||||
| chr2:231172353 | T | C | 1 | a0001c0005t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*10-182T>C | PSMD1 | ENSG00000173692.14 | transcript | ENST00000308696.11 | protein_coding | 24/24 | chr2 | 231172353 |