Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5636 |
| ensemblid | ENSG00000141127.15 |
| hgncid | 9467 |
| symbol | PRPSAP2 |
| name | phosphoribosyl pyrophosphate synthetase associated protein 2 |
| refseq_nuc | NM_002767.4 |
| refseq_prot | NP_002758.1 |
| ensembl_nuc | ENST00000268835.7 |
| ensembl_prot | ENSP00000268835.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 18858131 |
| end | 18931287 |
| strand | + |
| ver | v1.2 |
| region | chr17:18858131-18931287 |
| region5000 | chr17:18853131-18936287 |
| regionname0 | PRPSAP2_chr17_18858131_18931287 |
| regionname5000 | PRPSAP2_chr17_18853131_18936287 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1107 | 214 | 42 | 34 | 107 | 6 | 23 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | ATGTT others(1102): Show |
chr17 | 18853131 | 18936287 | ||
| a0001c0002 | 0/0 | 1107 | 168 | 42 | 45 | 56 | 6 | 19 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | ATGTT others(1102): Show |
chr17 | 18853131 | 18936287 | ||
| a0001c0003 | 0/0 | 1107 | 8 | 7 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | ATGTT others(1102): Show |
chr17 | 18853131 | 18936287 | ||
| a0001c0004 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | ATGTT others(1102): Show |
chr17 | 18853131 | 18936287 | ||
| a0001c0005 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | ATGTT others(1102): Show |
chr17 | 18853131 | 18936287 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1958 | 181 | 32 | 31 | 93 | 5 | 18 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0001t0002 | 0/0 | 1958 | 4 | 1 | 1 | 1 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0001t0005 | 0/0 | 1958 | 22 | 3 | 2 | 13 | 1 | 3 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0001t0006 | 0/0 | 1958 | 6 | 6 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0001t0010 | 0/0 | 1958 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0002t0002 | 0/0 | 1958 | 122 | 27 | 30 | 48 | 4 | 13 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0002t0003 | 0/0 | 1958 | 18 | 9 | 7 | 0 | 0 | 2 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0002t0004 | 0/0 | 1958 | 24 | 5 | 7 | 7 | 2 | 3 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0002t0007 | 0/0 | 1958 | 2 | 0 | 0 | 1 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0002t0008 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0002t0009 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0003t0003 | 0/0 | 1958 | 8 | 7 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0004t0005 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| a0001c0005t0002 | 0/0 | 1958 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | GCAGT others(1953): Show |
chr17 | 18853131 | 18936287 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0005g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0001t0010g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0007g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0007g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0002t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0003t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0004t0005g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| a0001c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0375 | EUR | GBR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | GBR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0139 | EUR | GBR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0086 | EUR | FIN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0360 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0369 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0366 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0020 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0362 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0377 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0049 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01106 | hp2 | a0001 | c0002 | t0004 | g0146 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0128 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0140 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0382 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0131 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0138 | AMR | PUR | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0095 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01255 | hp2 | a0001 | c0002 | t0008 | g0088 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0381 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01361 | hp2 | a0001 | c0002 | t0004 | g0141 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0134 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0144 | EUR | IBS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0129 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0030 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0023 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0080 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0148 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02258 | hp2 | a0001 | c0004 | t0005 | g0379 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0132 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0024 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0067 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0170 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02622 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0017 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0026 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0167 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0068 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0193 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02922 | hp1 | a0001 | c0002 | t0009 | g0179 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0166 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0127 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0374 | AFR | GWD | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0011 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0169 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0022 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03225 | hp2 | a0001 | c0003 | t0003 | g0010 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03239 | hp1 | a0001 | c0002 | t0007 | g0197 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0174 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0130 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0021 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0013 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0029 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0359 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | ESN | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0091 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0376 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0364 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03669 | hp2 | a0001 | c0002 | t0004 | g0149 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0105 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0388 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0143 | SAS | PJL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0119 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0084 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0150 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0110 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0118 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04184 | hp1 | a0001 | c0001 | t0010 | g0263 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | BEB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0107 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | YRI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | YRI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0027 | AFR | YRI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0370 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0142 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0371 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0363 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0133 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0387 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18974 | hp1 | a0001 | c0002 | t0004 | g0136 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18981 | hp2 | a0001 | c0002 | t0004 | g0145 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18999 | hp2 | a0001 | c0002 | t0004 | g0147 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0361 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0372 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19010 | hp2 | a0001 | c0005 | t0002 | g0057 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | LWK | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | LWK | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0390 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19056 | hp1 | a0001 | c0002 | t0004 | g0135 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0365 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0386 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19075 | hp2 | a0001 | c0002 | t0007 | g0358 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0368 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0383 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19087 | hp1 | a0001 | c0002 | t0004 | g0151 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0367 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | YRI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0164 | AFR | YRI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ASW | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0019 | AFR | ASW | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0066 | EUR | TSI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0047 | EUR | TSI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0096 | SAS | GIH | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | GIH | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0025 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0378 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0389 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | ACB | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0168 | AFR | USA | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0373 | AFR | USA | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0385 | EAS | JPT | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | USA | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | USA | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0162 | AFR | LWK | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0279 | REF | REF | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0232 | REF | REF | PRPSAP2_chr17_18853131_18936287 | PRPSAP2 | chr17 | 18853131 | 18936287 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:18865848 | G | A | 1 | a0001c0004 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.15G>A | p.Thr5Thr | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/12 | 274/1958 | 15/1110 | 5/369 | chr17 | 18865848 | |||
| chr17:18872587 | A | G | 3 | a0001c0002 a0001c0003 a0001c0005 |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
synonymous_variant | LOW | c.177A>G | p.Thr59Thr | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/12 | 436/1958 | 177/1110 | 59/369 | chr17 | 18872587 | |||
| chr17:18882570 | C | T | 1 | a0001c0003 | 8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.415C>T | p.Leu139Leu | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/12 | 674/1958 | 415/1110 | 139/369 | chr17 | 18882570 | |||
| chr17:18928909 | G | A | 1 | a0001c0005 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.903G>A | p.Leu301Leu | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/12 | 1162/1958 | 903/1110 | 301/369 | chr17 | 18928909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:18858195 | G | A | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0003 others(5): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
5_prime_UTR_variant | MODIFIER | c.-195G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/12 | 7639 | chr17 | 18858195 | ||||||
| chr17:18865557 | C | T | 3 | a0001c0001t0005 a0001c0002t0007 a0001c0004t0005 |
25 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 2/12 | 277 | chr17 | 18865557 | ||||||
| chr17:18930708 | T | C | 3 | a0001c0001t0006 a0001c0002t0003 a0001c0003t0003 |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 12/12 | 10 | chr17 | 18930708 | ||||||
| chr17:18930750 | T | C | 1 | a0001c0002t0008 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 12/12 | 52 | chr17 | 18930750 | ||||||
| chr17:18930783 | T | G | 1 | a0001c0001t0010 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 12/12 | 85 | chr17 | 18930783 | ||||||
| chr17:18930824 | A | T | 2 | a0001c0002t0004 a0001c0002t0007 |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*126A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 12/12 | 126 | chr17 | 18930824 | ||||||
| chr17:18930945 | G | T | 6 | a0001c0001t0006 a0001c0002t0003 a0001c0002t0004 others(3): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*247G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 12/12 | 247 | chr17 | 18930945 | ||||||
| chr17:18931239 | A | G | 3 | a0001c0001t0006 a0001c0002t0003 a0001c0003t0003 |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*541A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 12/12 | 541 | chr17 | 18931239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:18858346 | C | A | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-129+85C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18858346 | |||||||
| chr17:18858441 | T | C | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-129+180T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18858441 | |||||||
| chr17:18858514 | T | G | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-129+253T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18858514 | |||||||
| chr17:18858856 | T | TGAG | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-129+597_-129+599d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18858856 | ||||||
| chr17:18858865 | A | G | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-129+604A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18858865 | |||||||
| chr17:18858887 | A | T | 1 | a0001c0001t0001g0390 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-129+626A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18858887 | |||||||
| chr17:18858972 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-129+711T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18858972 | |||||||
| chr17:18858972 | T | G | 1 | a0001c0001t0001g0390 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-129+711T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18858972 | |||||||
| chr17:18859004 | G | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-129+743G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859004 | |||||||
| chr17:18859031 | A | T | 1 | a0001c0001t0001g0389 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-129+770A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859031 | |||||||
| chr17:18859273 | A | T | 1 | a0001c0001t0001g0390 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-129+1012A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859273 | |||||||
| chr17:18859608 | T | G | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | NA18959.hp2 NA18964.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-129+1347T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859608 | |||||||
| chr17:18859663 | C | A | 27 | a0001c0001t0002g0031 a0001c0002t0003g0013 a0001c0002t0003g0014 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-129+1402C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859663 | |||||||
| chr17:18859808 | G | A | 1 | a0001c0001t0005g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-129+1547G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859808 | |||||||
| chr17:18859824 | A | C | 1 | a0001c0001t0002g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-129+1563A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859824 | |||||||
| chr17:18859825 | A | G | 27 | a0001c0001t0002g0031 a0001c0002t0003g0013 a0001c0002t0003g0014 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-129+1564A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859825 | |||||||
| chr17:18859906 | G | A | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129+1645G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859906 | |||||||
| chr17:18859947 | C | T | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-129+1686C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18859947 | |||||||
| chr17:18860007 | G | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-129+1746G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860007 | |||||||
| chr17:18860011 | T | A | 1 | a0001c0001t0001g0390 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-129+1750T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860011 | |||||||
| chr17:18860104 | G | A | 1 | a0001c0001t0001g0390 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-129+1843G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860104 | |||||||
| chr17:18860118 | G | A | 1 | a0001c0003t0003g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-129+1857G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860118 | |||||||
| chr17:18860123 | G | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-129+1862G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860123 | |||||||
| chr17:18860319 | G | A | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129+2058G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860319 | |||||||
| chr17:18860593 | G | T | 1 | a0001c0002t0002g0178 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-129+2332G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860593 | |||||||
| chr17:18860653 | A | T | 1 | a0001c0002t0003g0030 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-129+2392A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860653 | |||||||
| chr17:18860663 | C | T | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129+2402C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860663 | |||||||
| chr17:18860764 | G | A | 97 | a0001c0001t0002g0112 a0001c0001t0002g0123 a0001c0002t0002g0001 others(94): Show |
98 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.-129+2503G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860764 | |||||||
| chr17:18860848 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-129+2587T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860848 | |||||||
| chr17:18860992 | A | C | 1 | a0001c0001t0001g0388 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-129+2731A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18860992 | |||||||
| chr17:18861072 | T | G | 27 | a0001c0001t0002g0031 a0001c0002t0003g0013 a0001c0002t0003g0014 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-129+2811T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861072 | |||||||
| chr17:18861148 | G | A | 1 | a0001c0002t0002g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-129+2887G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861148 | |||||||
| chr17:18861186 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-129+2925C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861186 | |||||||
| chr17:18861235 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-129+2974C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861235 | |||||||
| chr17:18861413 | G | A | 9 | a0001c0001t0001g0196 a0001c0003t0003g0005 a0001c0003t0003g0006 others(6): Show |
9 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129+3152G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861413 | |||||||
| chr17:18861424 | A | T | 1 | a0001c0001t0001g0387 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-129+3163A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861424 | |||||||
| chr17:18861464 | T | TA | 175 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.-129+3217dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18861464 | ||||||
| chr17:18861464 | TA | T | 7 | a0001c0001t0001g0380 a0001c0001t0001g0381 a0001c0001t0001g0382 others(4): Show |
7 | HG01169.hp1 HG01256.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.-129+3217delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18861464 | ||||||
| chr17:18861479 | G | A | 1 | a0001c0002t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-129+3218G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861479 | |||||||
| chr17:18861480 | A | G | 1 | a0001c0002t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-129+3219A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861480 | |||||||
| chr17:18861484 | A | G | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-129+3223A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861484 | |||||||
| chr17:18861689 | C | A | 1 | a0001c0002t0002g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-129+3428C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861689 | |||||||
| chr17:18861708 | A | G | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-129+3447A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861708 | |||||||
| chr17:18861883 | T | TTTTGTTT others(1): Show |
115 | a0001c0001t0002g0112 a0001c0001t0002g0171 a0001c0002t0002g0001 others(112): Show |
116 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.-128-3570_-128-356 others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18861883 | ||||||
| chr17:18861883 | T | TTTTGTTT others(5): Show |
43 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0002g0036 others(40): Show |
43 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-128-3574_-128-356 others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18861883 | ||||||
| chr17:18861883 | T | TTTTGTTT others(9): Show |
18 | a0001c0001t0002g0031 a0001c0002t0002g0033 a0001c0002t0003g0013 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-128-3578_-128-356 others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18861883 | ||||||
| chr17:18861883 | T | TTTTGTTT others(13): Show |
1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-128-3582_-128-356 others(24): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18861883 | ||||||
| chr17:18861991 | G | A | 16 | a0001c0002t0002g0001 a0001c0002t0002g0033 a0001c0002t0002g0034 others(13): Show |
17 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-128-3478G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18861991 | |||||||
| chr17:18862010 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-128-3459C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862010 | |||||||
| chr17:18862177 | G | T | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-128-3292G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862177 | |||||||
| chr17:18862213 | G | A | 2 | a0001c0002t0002g0044 a0001c0002t0002g0045 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-128-3256G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862213 | |||||||
| chr17:18862244 | A | G | 18 | a0001c0001t0002g0031 a0001c0002t0003g0013 a0001c0002t0003g0014 others(15): Show |
18 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.-128-3225A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862244 | |||||||
| chr17:18862451 | T | TAA | 152 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(149): Show |
153 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.-128-3011_-128-301 others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862451 | ||||||
| chr17:18862451 | T | TAAA | 26 | a0001c0002t0002g0137 a0001c0002t0004g0127 a0001c0002t0004g0128 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-128-3012_-128-301 others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862451 | ||||||
| chr17:18862466 | T | TC | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-2997dupC | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862466 | ||||||
| chr17:18862791 | T | TTTTA | 16 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0001g0199 others(13): Show |
16 | HG01074.hp1 HG01346.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-128-2638_-128-263 others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862791 | ||||||
| chr17:18862791 | T | TTTTATTT others(5): Show |
1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-128-2668_-128-266 others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862791 | ||||||
| chr17:18862791 | TTTTATTT others(1): Show |
T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0356 a0001c0001t0001g0357 |
4 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128-2642_-128-263 others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862791 | ||||||
| chr17:18862791 | TTTTATTT others(9): Show |
T | 25 | a0001c0001t0005g0189 a0001c0001t0005g0359 a0001c0001t0005g0360 others(22): Show |
25 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.-128-2650_-128-263 others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862791 | ||||||
| chr17:18862798 | T | TATTC | 42 | a0001c0001t0002g0171 a0001c0002t0002g0137 a0001c0002t0002g0167 others(39): Show |
42 | HG00140.hp2 HG00741.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.-128-2668_-128-266 others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18862798 | ||||||
| chr17:18862802 | T | C | 135 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(132): Show |
136 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.-128-2667T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862802 | |||||||
| chr17:18862827 | A | G | 27 | a0001c0001t0002g0031 a0001c0002t0003g0013 a0001c0002t0003g0014 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-128-2642A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862827 | |||||||
| chr17:18862853 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-128-2616C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862853 | |||||||
| chr17:18862906 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-128-2563C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862906 | |||||||
| chr17:18862993 | TG | T | 88 | a0001c0001t0001g0181 a0001c0001t0001g0205 a0001c0001t0001g0206 others(85): Show |
88 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.-128-2475delG | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862993 | |||||||
| chr17:18862994 | G | C | 1 | a0001c0002t0002g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-128-2475G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18862994 | |||||||
| chr17:18863069 | C | T | 21 | a0001c0002t0002g0137 a0001c0002t0004g0131 a0001c0002t0004g0132 others(18): Show |
21 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-128-2400C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863069 | |||||||
| chr17:18863142 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-128-2327T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863142 | |||||||
| chr17:18863181 | A | G | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-2288A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863181 | |||||||
| chr17:18863279 | C | G | 8 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-2190C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863279 | |||||||
| chr17:18863512 | C | G | 123 | a0001c0001t0002g0112 a0001c0001t0002g0123 a0001c0001t0002g0171 others(120): Show |
124 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-128-1957C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863512 | |||||||
| chr17:18863526 | C | CTCTTT | 30 | a0001c0001t0002g0031 a0001c0002t0002g0003 a0001c0002t0002g0004 others(27): Show |
30 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.-128-1927_-128-192 others(9): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18863526 | ||||||
| chr17:18863526 | CTCTTT | C | 148 | a0001c0001t0002g0112 a0001c0001t0002g0123 a0001c0001t0002g0171 others(145): Show |
149 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-128-1927_-128-192 others(9): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18863526 | ||||||
| chr17:18863556 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG00099.hp2 HG00733.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-128-1913G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863556 | |||||||
| chr17:18863565 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-128-1904C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863565 | |||||||
| chr17:18863701 | C | G | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-128-1768C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863701 | |||||||
| chr17:18863777 | A | T | 1 | a0001c0002t0003g0026 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-128-1692A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863777 | |||||||
| chr17:18863831 | C | CT | 15 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0352 others(12): Show |
15 | HG01069.hp2 HG01168.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.-128-1616dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18863831 | ||||||
| chr17:18863831 | C | CTT | 108 | a0001c0001t0001g0211 a0001c0001t0002g0123 a0001c0001t0002g0171 others(105): Show |
109 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-128-1617_-128-161 others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18863831 | ||||||
| chr17:18863831 | C | CTTT | 52 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0002t0002g0003 others(49): Show |
52 | HG00140.hp2 HG00423.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.-128-1618_-128-161 others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18863831 | ||||||
| chr17:18863831 | C | CTTTT | 9 | a0001c0002t0002g0004 a0001c0002t0002g0121 a0001c0002t0002g0122 others(6): Show |
9 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-1619_-128-161 others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18863831 | ||||||
| chr17:18863831 | CT | C | 9 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0198 others(6): Show |
9 | HG01074.hp1 HG01257.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-1616delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18863831 | ||||||
| chr17:18863853 | T | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0216 |
2 | HG01884.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-128-1616T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863853 | |||||||
| chr17:18863904 | A | C | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-1565A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18863904 | |||||||
| chr17:18864014 | T | A | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-128-1455T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864014 | |||||||
| chr17:18864131 | G | A | 1 | a0001c0002t0002g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-128-1338G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864131 | |||||||
| chr17:18864133 | C | T | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-1336C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864133 | |||||||
| chr17:18864205 | T | A | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-1264T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864205 | |||||||
| chr17:18864231 | C | T | 1 | a0001c0002t0002g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-128-1238C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864231 | |||||||
| chr17:18864296 | G | GT | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0275 others(4): Show |
7 | HG01109.hp1 HG01978.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-128-1160dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 18864296 | ||||||
| chr17:18864313 | A | G | 9 | a0001c0002t0003g0028 a0001c0003t0003g0005 a0001c0003t0003g0006 others(6): Show |
9 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-1156A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864313 | |||||||
| chr17:18864324 | C | T | 2 | a0001c0002t0002g0109 a0001c0002t0002g0110 |
2 | HG01952.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-128-1145C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864324 | |||||||
| chr17:18864396 | C | T | 1 | a0001c0001t0005g0378 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-128-1073C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864396 | |||||||
| chr17:18864443 | A | G | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-128-1026A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864443 | |||||||
| chr17:18864533 | C | T | 148 | a0001c0001t0002g0112 a0001c0001t0002g0123 a0001c0001t0002g0171 others(145): Show |
149 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-128-936C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864533 | |||||||
| chr17:18864579 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-128-890C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864579 | |||||||
| chr17:18864610 | G | A | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-859G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864610 | |||||||
| chr17:18864698 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-128-771C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864698 | |||||||
| chr17:18864699 | C | T | 88 | a0001c0001t0001g0181 a0001c0001t0001g0205 a0001c0001t0001g0206 others(85): Show |
88 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.-128-770C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864699 | |||||||
| chr17:18864826 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0219 |
2 | NA18992.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-128-643G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18864826 | |||||||
| chr17:18865059 | G | A | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-410G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18865059 | |||||||
| chr17:18865081 | G | A | 1 | a0001c0002t0002g0152 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-128-388G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18865081 | |||||||
| chr17:18865124 | C | T | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-345C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18865124 | |||||||
| chr17:18865149 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-128-320C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18865149 | |||||||
| chr17:18865269 | C | T | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-128-200C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18865269 | |||||||
| chr17:18865431 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-128-38C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 1/11 | chr17 | 18865431 | |||||||
| chr17:18865752 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-50G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 2/11 | chr17 | 18865752 | |||||||
| chr17:18866016 | G | A | 1 | a0001c0003t0003g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.119+64G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866016 | |||||||
| chr17:18866036 | T | C | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.119+84T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866036 | |||||||
| chr17:18866198 | G | A | 1 | a0001c0002t0003g0015 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.119+246G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866198 | |||||||
| chr17:18866206 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.119+254T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866206 | |||||||
| chr17:18866287 | A | G | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.119+335A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866287 | |||||||
| chr17:18866292 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.119+340C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866292 | |||||||
| chr17:18866355 | G | T | 2 | a0001c0001t0001g0350 a0001c0001t0001g0351 |
2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.119+403G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866355 | |||||||
| chr17:18866360 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.119+408T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866360 | |||||||
| chr17:18866391 | C | T | 27 | a0001c0001t0002g0031 a0001c0002t0003g0013 a0001c0002t0003g0014 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.119+439C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866391 | |||||||
| chr17:18866393 | C | T | 1 | a0001c0002t0002g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.119+441C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866393 | |||||||
| chr17:18866437 | A | G | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.119+485A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866437 | |||||||
| chr17:18866479 | G | A | 88 | a0001c0001t0001g0181 a0001c0001t0001g0205 a0001c0001t0001g0206 others(85): Show |
88 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.119+527G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866479 | |||||||
| chr17:18866527 | C | T | 88 | a0001c0001t0001g0181 a0001c0001t0001g0205 a0001c0001t0001g0206 others(85): Show |
88 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.119+575C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866527 | |||||||
| chr17:18866535 | G | A | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | HG00673.hp2 HG02135.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+583G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866535 | |||||||
| chr17:18866545 | C | T | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.119+593C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866545 | |||||||
| chr17:18866782 | A | G | 9 | a0001c0001t0002g0171 a0001c0002t0002g0167 a0001c0002t0002g0168 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.120-500A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866782 | |||||||
| chr17:18866941 | A | G | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.120-341A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866941 | |||||||
| chr17:18866943 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.120-339C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866943 | |||||||
| chr17:18866970 | C | G | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.120-312C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18866970 | |||||||
| chr17:18867054 | A | G | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.120-228A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18867054 | |||||||
| chr17:18867164 | A | G | 1 | a0001c0001t0005g0377 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.120-118A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18867164 | |||||||
| chr17:18867217 | A | G | 88 | a0001c0001t0001g0181 a0001c0001t0001g0205 a0001c0001t0001g0206 others(85): Show |
88 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.120-65A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 3/11 | chr17 | 18867217 | |||||||
| chr17:18867394 | C | T | 8 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(5): Show |
8 | NA18947.hp1 NA18949.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.172+60C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18867394 | |||||||
| chr17:18867395 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+61G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18867395 | |||||||
| chr17:18867420 | G | A | 178 | a0001c0001t0002g0031 a0001c0001t0002g0112 a0001c0001t0002g0123 others(175): Show |
179 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.172+86G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18867420 | |||||||
| chr17:18867427 | T | C | 1 | a0001c0001t0005g0378 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.172+93T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18867427 | |||||||
| chr17:18867732 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172+398G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18867732 | |||||||
| chr17:18867832 | G | A | 179 | a0001c0001t0001g0180 a0001c0001t0002g0031 a0001c0001t0002g0112 others(176): Show |
180 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.172+498G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18867832 | |||||||
| chr17:18867855 | G | A | 25 | a0001c0002t0002g0137 a0001c0002t0004g0127 a0001c0002t0004g0128 others(22): Show |
25 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.172+521G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18867855 | |||||||
| chr17:18868112 | T | C | 123 | a0001c0001t0002g0112 a0001c0001t0002g0123 a0001c0001t0002g0171 others(120): Show |
124 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.172+778T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868112 | |||||||
| chr17:18868117 | AAAATAAA others(1): Show |
A | 21 | a0001c0002t0002g0137 a0001c0002t0004g0131 a0001c0002t0004g0132 others(18): Show |
21 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.172+797_172+804del others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18868117 | ||||||
| chr17:18868167 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172+833A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868167 | |||||||
| chr17:18868272 | G | A | 1 | a0001c0002t0002g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.172+938G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868272 | |||||||
| chr17:18868359 | C | A | 24 | a0001c0001t0005g0189 a0001c0001t0005g0359 a0001c0001t0005g0360 others(21): Show |
24 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.172+1025C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868359 | |||||||
| chr17:18868371 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.172+1037A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868371 | |||||||
| chr17:18868462 | GAGCGAGA others(40): Show |
G | 1 | a0001c0002t0002g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.172+1132_172+1178d others(49): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18868462 | ||||||
| chr17:18868483 | G | GA | 6 | a0001c0001t0001g0258 a0001c0001t0001g0348 a0001c0001t0010g0263 others(3): Show |
6 | HG00741.hp2 HG02258.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+1164dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18868483 | ||||||
| chr17:18868513 | A | T | 1 | a0001c0002t0002g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.172+1179A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868513 | |||||||
| chr17:18868519 | G | T | 1 | a0001c0002t0002g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.172+1185G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868519 | |||||||
| chr17:18868520 | A | C | 1 | a0001c0002t0002g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.172+1186A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868520 | |||||||
| chr17:18868547 | T | C | 1 | a0001c0002t0003g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172+1213T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868547 | |||||||
| chr17:18868663 | C | T | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+1329C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868663 | |||||||
| chr17:18868680 | A | G | 27 | a0001c0001t0002g0031 a0001c0002t0003g0013 a0001c0002t0003g0014 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.172+1346A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868680 | |||||||
| chr17:18868723 | A | AT | 104 | a0001c0001t0001g0181 a0001c0001t0001g0199 a0001c0001t0001g0203 others(101): Show |
104 | HG00642.hp2 HG00673.hp2 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.172+1403dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18868723 | ||||||
| chr17:18868723 | A | ATT | 156 | a0001c0001t0001g0180 a0001c0001t0001g0210 a0001c0001t0001g0211 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.172+1402_172+1403d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18868723 | ||||||
| chr17:18868723 | A | ATTT | 19 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 others(16): Show |
19 | HG01175.hp1 HG01257.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+1401_172+1403d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18868723 | ||||||
| chr17:18868729 | T | A | 1 | a0001c0003t0003g0008 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+1395T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868729 | |||||||
| chr17:18868746 | A | G | 186 | a0001c0001t0001g0202 a0001c0001t0001g0266 a0001c0001t0001g0346 others(183): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.172+1412A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868746 | |||||||
| chr17:18868787 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.172+1453G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868787 | |||||||
| chr17:18868815 | C | G | 2 | a0001c0001t0010g0263 a0001c0002t0002g0103 |
2 | HG04184.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.172+1481C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18868815 | |||||||
| chr17:18869341 | C | CT | 117 | a0001c0001t0001g0321 a0001c0001t0002g0171 a0001c0001t0005g0373 others(114): Show |
118 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.172+2021dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869341 | ||||||
| chr17:18869341 | CT | C | 11 | a0001c0001t0001g0380 a0001c0001t0005g0359 a0001c0002t0003g0028 others(8): Show |
11 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+2021delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869341 | ||||||
| chr17:18869503 | A | AT | 104 | a0001c0001t0001g0181 a0001c0001t0001g0203 a0001c0001t0001g0204 others(101): Show |
104 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.172+2185dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869503 | ||||||
| chr17:18869576 | C | T | 1 | a0001c0002t0002g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+2242C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869576 | |||||||
| chr17:18869601 | C | T | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+2267C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869601 | |||||||
| chr17:18869612 | C | T | 8 | a0001c0001t0001g0180 a0001c0001t0006g0190 a0001c0001t0006g0191 others(5): Show |
8 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.172+2278C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869612 | |||||||
| chr17:18869654 | T | C | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.172+2320T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869654 | |||||||
| chr17:18869697 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.172+2363G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869697 | |||||||
| chr17:18869789 | AT | A | 132 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0199 others(129): Show |
132 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.172+2466delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869789 | ||||||
| chr17:18869789 | ATT | A | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.172+2465_172+2466d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869789 | ||||||
| chr17:18869834 | C | CTT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0221 a0001c0001t0001g0260 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.172+2508_172+2509d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869834 | ||||||
| chr17:18869836 | T | TGTGTGTG others(8): Show |
1 | a0001c0002t0002g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.172+2502_172+2503i others(17): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869836 | |||||||
| chr17:18869836 | T | TTGTGTG | 6 | a0001c0002t0002g0004 a0001c0002t0002g0065 a0001c0002t0004g0127 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+2503_172+2504i others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869836 | T | TTGTGTGT others(1): Show |
12 | a0001c0002t0002g0003 a0001c0002t0002g0108 a0001c0002t0004g0132 others(9): Show |
12 | HG00741.hp2 HG01261.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+2503_172+2504i others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869836 | T | TTGTGTGT others(3): Show |
20 | a0001c0002t0002g0056 a0001c0002t0002g0066 a0001c0002t0002g0137 others(17): Show |
20 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.172+2503_172+2504i others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869836 | T | TTGTGTGT others(5): Show |
70 | a0001c0002t0002g0001 a0001c0002t0002g0032 a0001c0002t0002g0033 others(67): Show |
71 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.172+2503_172+2504i others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869836 | T | TTGTGTGT others(7): Show |
41 | a0001c0001t0002g0171 a0001c0002t0002g0035 a0001c0002t0002g0041 others(38): Show |
41 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.172+2503_172+2504i others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869836 | T | TTGTGTGT others(9): Show |
6 | a0001c0002t0002g0063 a0001c0002t0002g0101 a0001c0002t0002g0111 others(3): Show |
6 | HG01167.hp2 HG01192.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+2503_172+2504i others(18): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869836 | T | TTGTGTGT others(11): Show |
3 | a0001c0002t0002g0059 a0001c0002t0002g0126 a0001c0002t0002g0164 |
3 | HG02738.hp1 NA18984.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.172+2503_172+2504i others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869836 | T | TTGTGTGT others(13): Show |
1 | a0001c0002t0002g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.172+2503_172+2504i others(22): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869836 | ||||||
| chr17:18869838 | T | G | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.172+2504T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869838 | |||||||
| chr17:18869840 | T | G | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.172+2506T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869840 | |||||||
| chr17:18869842 | T | G | 198 | a0001c0001t0001g0220 a0001c0001t0001g0224 a0001c0001t0002g0112 others(195): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.172+2508T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869842 | |||||||
| chr17:18869844 | G | T | 104 | a0001c0001t0001g0181 a0001c0001t0001g0198 a0001c0001t0001g0199 others(101): Show |
104 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.172+2510G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869844 | |||||||
| chr17:18869846 | G | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG03471.hp2 HG03579.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+2512G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869846 | |||||||
| chr17:18869865 | T | TGTGTGTG others(9): Show |
13 | a0001c0002t0003g0013 a0001c0002t0003g0017 a0001c0002t0003g0018 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.172+2532_172+2533i others(18): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869865 | ||||||
| chr17:18869865 | T | TGTGTGTG others(11): Show |
4 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(1): Show |
4 | HG01123.hp2 HG01168.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+2532_172+2533i others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18869865 | ||||||
| chr17:18869867 | A | T | 1 | a0001c0002t0002g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.172+2533A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869867 | |||||||
| chr17:18869933 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172+2599C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18869933 | |||||||
| chr17:18870008 | C | T | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-2575C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870008 | |||||||
| chr17:18870136 | A | G | 2 | a0001c0002t0002g0047 a0001c0002t0002g0050 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.173-2447A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870136 | |||||||
| chr17:18870195 | C | G | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.173-2388C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870195 | |||||||
| chr17:18870323 | T | C | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.173-2260T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870323 | |||||||
| chr17:18870338 | G | A | 56 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0137 others(53): Show |
56 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.173-2245G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870338 | |||||||
| chr17:18870340 | A | C | 3 | a0001c0002t0002g0154 a0001c0002t0002g0155 a0001c0002t0002g0156 |
3 | HG01433.hp2 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.173-2243A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870340 | |||||||
| chr17:18870768 | C | T | 1 | a0001c0002t0004g0144 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.173-1815C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870768 | |||||||
| chr17:18870784 | G | A | 176 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.173-1799G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870784 | |||||||
| chr17:18870808 | C | CA | 7 | a0001c0001t0001g0211 a0001c0001t0001g0225 a0001c0001t0001g0321 others(4): Show |
7 | HG01256.hp2 HG02523.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.173-1759dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18870808 | ||||||
| chr17:18870808 | CAAA | C | 172 | a0001c0002t0002g0001 a0001c0002t0002g0032 a0001c0002t0002g0033 others(169): Show |
173 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.173-1761_173-1759d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18870808 | ||||||
| chr17:18870958 | A | G | 176 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.173-1625A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18870958 | |||||||
| chr17:18871070 | A | C | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.173-1513A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871070 | |||||||
| chr17:18871290 | T | G | 176 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.173-1293T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871290 | |||||||
| chr17:18871395 | A | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0181 others(314): Show |
319 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.173-1188A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871395 | |||||||
| chr17:18871534 | A | G | 1 | a0001c0002t0002g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.173-1049A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871534 | |||||||
| chr17:18871653 | C | CT | 10 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0204 others(7): Show |
10 | HG00741.hp1 HG03471.hp2 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.173-906dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18871653 | ||||||
| chr17:18871653 | CT | C | 12 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0277 others(9): Show |
12 | HG00323.hp1 HG01070.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.173-906delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18871653 | ||||||
| chr17:18871653 | CTTTTTTT others(2): Show |
C | 175 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.173-914_173-906del others(9): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18871653 | ||||||
| chr17:18871653 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0007g0358 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.173-915_173-906del others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18871653 | ||||||
| chr17:18871667 | T | C | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.173-916T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871667 | |||||||
| chr17:18871669 | T | C | 176 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.173-914T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871669 | |||||||
| chr17:18871849 | G | A | 3 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 |
3 | HG02055.hp2 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.173-734G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871849 | |||||||
| chr17:18871849 | G | C | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.173-734G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871849 | |||||||
| chr17:18871967 | G | A | 4 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | NA18983.hp1 NA18988.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-616G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18871967 | |||||||
| chr17:18872009 | A | G | 176 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.173-574A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872009 | |||||||
| chr17:18872050 | C | T | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-533C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872050 | |||||||
| chr17:18872053 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.173-530G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872053 | |||||||
| chr17:18872122 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.173-461A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872122 | |||||||
| chr17:18872142 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.173-441G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872142 | |||||||
| chr17:18872150 | G | A | 27 | a0001c0002t0002g0137 a0001c0002t0004g0127 a0001c0002t0004g0128 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.173-433G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872150 | |||||||
| chr17:18872170 | G | A | 8 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.173-413G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872170 | |||||||
| chr17:18872248 | G | A | 120 | a0001c0002t0002g0001 a0001c0002t0002g0032 a0001c0002t0002g0033 others(117): Show |
121 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.173-335G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872248 | |||||||
| chr17:18872252 | G | A | 147 | a0001c0002t0002g0001 a0001c0002t0002g0032 a0001c0002t0002g0033 others(144): Show |
148 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.173-331G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872252 | |||||||
| chr17:18872268 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.173-315G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872268 | |||||||
| chr17:18872272 | CA | C | 10 | a0001c0001t0001g0183 a0001c0001t0001g0217 a0001c0001t0001g0218 others(7): Show |
10 | HG00558.hp2 HG01169.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.173-293delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 18872272 | ||||||
| chr17:18872291 | G | A | 93 | a0001c0001t0001g0181 a0001c0001t0001g0205 a0001c0001t0001g0206 others(90): Show |
93 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.173-292G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872291 | |||||||
| chr17:18872554 | C | T | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-29C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 4/11 | chr17 | 18872554 | |||||||
| chr17:18872705 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.239+56A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18872705 | |||||||
| chr17:18872707 | A | T | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.239+58A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18872707 | |||||||
| chr17:18873077 | C | G | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.239+428C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873077 | |||||||
| chr17:18873135 | T | TCCAGCCA others(6063): Show |
1 | a0001c0002t0002g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.239+505_239+506ins others(6070): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18873135 | ||||||
| chr17:18873191 | C | CT | 127 | a0001c0001t0001g0182 a0001c0001t0001g0188 a0001c0001t0001g0200 others(124): Show |
128 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.239+561dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18873191 | ||||||
| chr17:18873191 | C | CTT | 52 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0034 others(49): Show |
52 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.239+560_239+561dup others(2): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18873191 | ||||||
| chr17:18873256 | C | T | 5 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(2): Show |
5 | HG01928.hp1 HG01943.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+607C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873256 | |||||||
| chr17:18873259 | T | TCTCGGCT others(9): Show |
177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.239+614_239+629dup others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18873259 | ||||||
| chr17:18873367 | C | T | 1 | a0001c0002t0004g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.239+718C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873367 | |||||||
| chr17:18873449 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.239+800A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873449 | |||||||
| chr17:18873584 | A | G | 303 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0199 others(300): Show |
304 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.239+935A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873584 | |||||||
| chr17:18873720 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.239+1071T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873720 | |||||||
| chr17:18873750 | G | A | 1 | a0001c0002t0002g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.239+1101G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873750 | |||||||
| chr17:18873875 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.239+1226G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18873875 | |||||||
| chr17:18873894 | C | CT | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | NA18959.hp2 NA18964.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1256dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18873894 | ||||||
| chr17:18874071 | G | A | 2 | a0001c0001t0010g0263 a0001c0002t0009g0179 |
2 | HG02922.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.239+1422G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18874071 | |||||||
| chr17:18874213 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0381 |
2 | HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.239+1564C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18874213 | |||||||
| chr17:18874285 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.239+1636G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18874285 | |||||||
| chr17:18874297 | T | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0381 |
2 | HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.239+1648T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18874297 | |||||||
| chr17:18874656 | A | G | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.239+2007A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18874656 | |||||||
| chr17:18874830 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+2181G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18874830 | |||||||
| chr17:18875098 | T | G | 1 | a0001c0001t0002g0112 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.239+2449T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18875098 | |||||||
| chr17:18875108 | C | T | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.239+2459C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18875108 | |||||||
| chr17:18875180 | A | G | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.240-2518A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18875180 | |||||||
| chr17:18875724 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.240-1974T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18875724 | |||||||
| chr17:18875817 | A | G | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.240-1881A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18875817 | |||||||
| chr17:18875853 | C | CA | 13 | a0001c0001t0001g0002 a0001c0001t0001g0221 a0001c0001t0001g0228 others(10): Show |
14 | HG01099.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.240-1828dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18875853 | ||||||
| chr17:18875853 | CA | C | 155 | a0001c0001t0001g0183 a0001c0001t0001g0254 a0001c0002t0002g0001 others(152): Show |
156 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.240-1828delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18875853 | ||||||
| chr17:18875958 | A | G | 1 | a0001c0002t0002g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.240-1740A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18875958 | |||||||
| chr17:18875963 | C | T | 3 | a0001c0001t0005g0367 a0001c0001t0005g0371 a0001c0001t0005g0372 |
3 | NA18960.hp2 NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.240-1735C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18875963 | |||||||
| chr17:18876338 | C | G | 1 | a0001c0001t0005g0370 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.240-1360C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18876338 | |||||||
| chr17:18876462 | A | G | 27 | a0001c0002t0002g0137 a0001c0002t0004g0127 a0001c0002t0004g0128 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.240-1236A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18876462 | |||||||
| chr17:18876856 | A | C | 1 | a0001c0002t0004g0142 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.240-842A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18876856 | |||||||
| chr17:18877006 | C | T | 2 | a0001c0002t0002g0105 a0001c0002t0002g0118 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.240-692C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18877006 | |||||||
| chr17:18877049 | C | T | 4 | a0001c0002t0004g0131 a0001c0002t0004g0134 a0001c0002t0004g0140 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.240-649C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18877049 | |||||||
| chr17:18877102 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0001g0292 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.240-596A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18877102 | |||||||
| chr17:18877118 | T | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.240-580T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18877118 | |||||||
| chr17:18877180 | C | T | 1 | a0001c0001t0001g0389 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240-518C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18877180 | |||||||
| chr17:18877245 | CAGCAAAG others(3): Show |
C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.240-448_240-439del others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18877245 | ||||||
| chr17:18877482 | C | T | 4 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0320 others(1): Show |
4 | HG02922.hp1 NA18954.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-216C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18877482 | |||||||
| chr17:18877538 | C | G | 3 | a0001c0002t0002g0154 a0001c0002t0002g0155 a0001c0002t0002g0156 |
3 | HG01433.hp2 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.240-160C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | chr17 | 18877538 | |||||||
| chr17:18877575 | GT | G | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.240-116delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 18877575 | ||||||
| chr17:18877878 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.412+8T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18877878 | |||||||
| chr17:18877909 | G | C | 5 | a0001c0001t0001g0198 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+39G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18877909 | |||||||
| chr17:18877931 | C | T | 4 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+61C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18877931 | |||||||
| chr17:18878178 | G | T | 1 | a0001c0002t0004g0151 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.412+308G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878178 | |||||||
| chr17:18878364 | T | TATA | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.412+495_412+497dup others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 18878364 | ||||||
| chr17:18878369 | C | T | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.412+499C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878369 | |||||||
| chr17:18878421 | G | A | 8 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0006g0190 others(5): Show |
8 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.412+551G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878421 | |||||||
| chr17:18878496 | T | G | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+626T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878496 | |||||||
| chr17:18878587 | C | T | 1 | a0001c0002t0002g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.412+717C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878587 | |||||||
| chr17:18878628 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.412+758G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878628 | |||||||
| chr17:18878635 | A | G | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+765A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878635 | |||||||
| chr17:18878782 | C | T | 1 | a0001c0002t0004g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.412+912C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878782 | |||||||
| chr17:18878790 | C | T | 1 | a0001c0001t0005g0378 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.412+920C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878790 | |||||||
| chr17:18878824 | G | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.412+954G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878824 | |||||||
| chr17:18878855 | T | A | 5 | a0001c0002t0002g0063 a0001c0002t0002g0064 a0001c0002t0002g0068 others(2): Show |
5 | HG01167.hp2 HG01361.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+985T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878855 | |||||||
| chr17:18878898 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.412+1028C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878898 | |||||||
| chr17:18878938 | C | T | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.412+1068C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878938 | |||||||
| chr17:18878988 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.412+1118G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878988 | |||||||
| chr17:18878994 | C | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.412+1124C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18878994 | |||||||
| chr17:18879164 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.412+1294C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879164 | |||||||
| chr17:18879191 | G | A | 1 | a0001c0002t0002g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.412+1321G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879191 | |||||||
| chr17:18879219 | G | C | 1 | a0001c0002t0002g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.412+1349G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879219 | |||||||
| chr17:18879269 | C | T | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1399C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879269 | |||||||
| chr17:18879378 | G | A | 145 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(142): Show |
146 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.412+1508G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879378 | |||||||
| chr17:18879479 | G | GAGTC | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1610_412+1613d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 18879479 | ||||||
| chr17:18879530 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.412+1660C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879530 | |||||||
| chr17:18879552 | T | C | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1682T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879552 | |||||||
| chr17:18879597 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.412+1727G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879597 | |||||||
| chr17:18879707 | G | C | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02074.hp1 HG02523.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.412+1837G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879707 | |||||||
| chr17:18879734 | G | A | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1864G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879734 | |||||||
| chr17:18879739 | C | A | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1869C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879739 | |||||||
| chr17:18879746 | G | A | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1876G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879746 | |||||||
| chr17:18879928 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.412+2058C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879928 | |||||||
| chr17:18879998 | A | T | 1 | a0001c0002t0002g0103 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.412+2128A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18879998 | |||||||
| chr17:18880051 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0312 |
2 | NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.412+2181A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880051 | |||||||
| chr17:18880092 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.412+2222G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880092 | |||||||
| chr17:18880325 | A | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.413-2243A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880325 | |||||||
| chr17:18880521 | C | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.413-2047C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880521 | |||||||
| chr17:18880660 | C | T | 1 | a0001c0002t0003g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.413-1908C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880660 | |||||||
| chr17:18880796 | C | T | 1 | a0001c0002t0003g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.413-1772C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880796 | |||||||
| chr17:18880851 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.413-1717C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880851 | |||||||
| chr17:18880858 | G | C | 1 | a0001c0002t0002g0157 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.413-1710G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18880858 | |||||||
| chr17:18881035 | T | C | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-1533T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881035 | |||||||
| chr17:18881091 | T | C | 185 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0002g0171 others(182): Show |
186 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.413-1477T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881091 | |||||||
| chr17:18881175 | TA | T | 152 | a0001c0001t0001g0183 a0001c0001t0001g0326 a0001c0001t0001g0333 others(149): Show |
153 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.413-1380delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 18881175 | ||||||
| chr17:18881188 | AT | A | 28 | a0001c0001t0001g0298 a0001c0002t0002g0003 a0001c0002t0002g0004 others(25): Show |
28 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-1372delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 18881188 | ||||||
| chr17:18881189 | T | A | 1 | a0001c0001t0001g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413-1379T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881189 | |||||||
| chr17:18881190 | T | A | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-1378T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881190 | |||||||
| chr17:18881191 | T | A | 1 | a0001c0002t0003g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.413-1377T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881191 | |||||||
| chr17:18881327 | C | G | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-1241C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881327 | |||||||
| chr17:18881489 | C | T | 1 | a0001c0001t0005g0375 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.413-1079C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881489 | |||||||
| chr17:18881491 | GCCTCCCA others(594): Show |
G | 6 | a0001c0001t0001g0326 a0001c0001t0001g0334 a0001c0001t0001g0335 others(3): Show |
6 | HG02027.hp1 HG02083.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-1041_413-441de others(1): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 18881491 | ||||||
| chr17:18881518 | G | A | 2 | a0001c0002t0004g0131 a0001c0002t0004g0140 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.413-1050G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881518 | |||||||
| chr17:18881530 | G | A | 1 | a0001c0001t0006g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.413-1038G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881530 | |||||||
| chr17:18881813 | G | A | 177 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(174): Show |
178 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.413-755G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881813 | |||||||
| chr17:18881820 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0221 a0001c0001t0001g0260 others(2): Show |
6 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-748A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881820 | |||||||
| chr17:18881842 | AT | A | 176 | a0001c0001t0001g0302 a0001c0001t0002g0171 a0001c0002t0002g0001 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.413-710delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 18881842 | ||||||
| chr17:18881915 | A | G | 1 | a0001c0001t0005g0378 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.413-653A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18881915 | |||||||
| chr17:18882170 | A | G | 2 | a0001c0001t0005g0373 a0001c0001t0005g0374 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.413-398A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18882170 | |||||||
| chr17:18882226 | T | C | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.413-342T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18882226 | |||||||
| chr17:18882402 | T | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.413-166T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 6/11 | chr17 | 18882402 | |||||||
| chr17:18882744 | A | G | 1 | a0001c0002t0002g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.528+61A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18882744 | |||||||
| chr17:18882786 | G | A | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+103G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18882786 | |||||||
| chr17:18883019 | A | G | 1 | a0001c0002t0002g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.528+336A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883019 | |||||||
| chr17:18883403 | C | CT | 77 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0001g0187 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.528+735dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18883403 | ||||||
| chr17:18883403 | C | CTT | 146 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(143): Show |
147 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.528+734_528+735dup others(2): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18883403 | ||||||
| chr17:18883403 | C | CTTT | 10 | a0001c0002t0002g0170 a0001c0002t0009g0179 a0001c0003t0003g0005 others(7): Show |
10 | HG00741.hp2 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.528+733_528+735dup others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18883403 | ||||||
| chr17:18883422 | G | T | 2 | a0001c0002t0002g0160 a0001c0002t0002g0161 |
2 | HG02132.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.528+739G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883422 | |||||||
| chr17:18883463 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.528+780C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883463 | |||||||
| chr17:18883463 | C | T | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+780C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883463 | |||||||
| chr17:18883507 | A | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG03927.hp2 NA18973.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.528+824A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883507 | |||||||
| chr17:18883536 | C | T | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+853C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883536 | |||||||
| chr17:18883664 | G | T | 8 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+981G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883664 | |||||||
| chr17:18883665 | C | T | 8 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+982C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883665 | |||||||
| chr17:18883691 | G | T | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+1008G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883691 | |||||||
| chr17:18883788 | T | A | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+1105T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883788 | |||||||
| chr17:18883869 | C | G | 147 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(144): Show |
148 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.528+1186C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18883869 | |||||||
| chr17:18884006 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.528+1323C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884006 | |||||||
| chr17:18884105 | T | C | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+1422T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884105 | |||||||
| chr17:18884190 | C | T | 2 | a0001c0002t0002g0164 a0001c0002t0002g0165 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.528+1507C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884190 | |||||||
| chr17:18884277 | A | AAGAAAAC others(18): Show |
1 | a0001c0001t0001g0384 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.528+1595_528+1619d others(27): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18884277 | ||||||
| chr17:18884346 | GT | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0183 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.528+1673delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18884346 | ||||||
| chr17:18884347 | T | G | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.528+1664T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884347 | |||||||
| chr17:18884369 | TTCTC | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0249 a0001c0001t0001g0264 others(1): Show |
4 | HG01175.hp2 HG01256.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+1688_528+1691d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18884369 | ||||||
| chr17:18884403 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.528+1720A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884403 | |||||||
| chr17:18884467 | G | A | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+1784G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884467 | |||||||
| chr17:18884468 | T | C | 2 | a0001c0002t0002g0109 a0001c0002t0002g0110 |
2 | HG01952.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.528+1785T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884468 | |||||||
| chr17:18884483 | G | A | 1 | a0001c0002t0002g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.528+1800G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884483 | |||||||
| chr17:18884515 | A | C | 119 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(116): Show |
120 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.528+1832A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884515 | |||||||
| chr17:18884618 | G | A | 119 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(116): Show |
120 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.528+1935G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884618 | |||||||
| chr17:18884663 | T | C | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+1980T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884663 | |||||||
| chr17:18884884 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.528+2201A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884884 | |||||||
| chr17:18884905 | A | G | 28 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0004g0127 others(25): Show |
28 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.528+2222A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884905 | |||||||
| chr17:18884909 | C | T | 1 | a0001c0002t0004g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.528+2226C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884909 | |||||||
| chr17:18884969 | C | T | 3 | a0001c0002t0003g0017 a0001c0002t0003g0021 a0001c0002t0003g0022 |
3 | HG02630.hp1 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.528+2286C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18884969 | |||||||
| chr17:18885246 | T | C | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+2563T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885246 | |||||||
| chr17:18885403 | C | CA | 54 | a0001c0001t0001g0181 a0001c0001t0001g0185 a0001c0001t0001g0186 others(51): Show |
54 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.528+2746dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18885403 | ||||||
| chr17:18885403 | C | CACAAA | 18 | a0001c0002t0004g0128 a0001c0002t0004g0130 a0001c0002t0004g0131 others(15): Show |
18 | HG00140.hp2 HG01109.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.528+2721_528+2722i others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18885403 | ||||||
| chr17:18885403 | CA | C | 8 | a0001c0001t0001g0180 a0001c0001t0005g0373 a0001c0001t0005g0374 others(5): Show |
8 | HG02055.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+2746delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18885403 | ||||||
| chr17:18885403 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0318 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.528+2737_528+2746d others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18885403 | ||||||
| chr17:18885429 | A | AAAAAAAT | 8 | a0001c0002t0002g0037 a0001c0002t0002g0043 a0001c0002t0002g0053 others(5): Show |
8 | HG01257.hp2 HG01261.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+2746_528+2747i others(9): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885429 | |||||||
| chr17:18885429 | A | AAAAAAT | 50 | a0001c0001t0002g0171 a0001c0002t0002g0003 a0001c0002t0002g0004 others(47): Show |
50 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.528+2746_528+2747i others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885429 | |||||||
| chr17:18885429 | A | AAAAAT | 69 | a0001c0002t0002g0001 a0001c0002t0002g0034 a0001c0002t0002g0036 others(66): Show |
70 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.528+2746_528+2747i others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885429 | |||||||
| chr17:18885429 | A | AAAAT | 17 | a0001c0002t0002g0083 a0001c0002t0003g0013 a0001c0002t0003g0016 others(14): Show |
17 | HG00642.hp2 HG00741.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.528+2746_528+2747i others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885429 | |||||||
| chr17:18885429 | A | T | 28 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0004g0127 others(25): Show |
28 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.528+2746A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885429 | |||||||
| chr17:18885434 | T | A | 6 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0361 others(3): Show |
6 | HG00423.hp1 HG00673.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+2751T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885434 | |||||||
| chr17:18885550 | G | A | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.528+2867G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885550 | |||||||
| chr17:18885674 | C | A | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.528+2991C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885674 | |||||||
| chr17:18885792 | G | A | 1 | a0001c0002t0003g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.528+3109G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885792 | |||||||
| chr17:18885864 | G | T | 20 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0359 others(17): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.528+3181G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885864 | |||||||
| chr17:18885923 | G | A | 1 | a0001c0002t0002g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.528+3240G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885923 | |||||||
| chr17:18885970 | G | A | 28 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0004g0127 others(25): Show |
28 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.528+3287G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18885970 | |||||||
| chr17:18886042 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.528+3359A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886042 | |||||||
| chr17:18886099 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.528+3416A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886099 | |||||||
| chr17:18886151 | T | TAGCAAAT others(20): Show |
1 | a0001c0002t0008g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.528+3468_528+3469i others(29): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886151 | |||||||
| chr17:18886153 | A | T | 1 | a0001c0002t0008g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.528+3470A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886153 | |||||||
| chr17:18886154 | C | T | 1 | a0001c0002t0008g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.528+3471C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886154 | |||||||
| chr17:18886227 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.528+3544T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886227 | |||||||
| chr17:18886274 | C | G | 1 | a0001c0002t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.529-3548C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886274 | |||||||
| chr17:18886302 | C | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.529-3520C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886302 | |||||||
| chr17:18886340 | G | A | 6 | a0001c0002t0004g0131 a0001c0002t0004g0134 a0001c0002t0004g0140 others(3): Show |
6 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-3482G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886340 | |||||||
| chr17:18886358 | A | T | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.529-3464A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886358 | |||||||
| chr17:18886359 | C | CT | 17 | a0001c0001t0002g0171 a0001c0002t0002g0038 a0001c0002t0002g0152 others(14): Show |
17 | HG01891.hp2 HG02132.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.529-3449dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18886359 | ||||||
| chr17:18886405 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.529-3417G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886405 | |||||||
| chr17:18886411 | A | G | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.529-3411A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886411 | |||||||
| chr17:18886416 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529-3406C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886416 | |||||||
| chr17:18886448 | C | T | 1 | a0001c0002t0004g0150 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.529-3374C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886448 | |||||||
| chr17:18886593 | A | G | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.529-3229A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886593 | |||||||
| chr17:18886604 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.529-3218C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886604 | |||||||
| chr17:18886650 | G | A | 12 | a0001c0001t0001g0226 a0001c0001t0001g0233 a0001c0001t0001g0236 others(9): Show |
12 | HG00323.hp1 HG01123.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.529-3172G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886650 | |||||||
| chr17:18886682 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.529-3140C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886682 | |||||||
| chr17:18886929 | C | CT | 32 | a0001c0001t0001g0187 a0001c0001t0001g0198 a0001c0001t0001g0199 others(29): Show |
32 | HG00423.hp1 HG00558.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.529-2869dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18886929 | ||||||
| chr17:18886929 | C | CTTTTT | 15 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(12): Show |
15 | HG00642.hp2 HG01123.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.529-2873_529-2869d others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18886929 | ||||||
| chr17:18886929 | CT | C | 8 | a0001c0001t0001g0205 a0001c0001t0001g0209 a0001c0001t0001g0310 others(5): Show |
8 | HG01256.hp2 HG02129.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.529-2869delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18886929 | ||||||
| chr17:18886929 | CTT | C | 6 | a0001c0002t0002g0068 a0001c0002t0002g0121 a0001c0002t0002g0160 others(3): Show |
6 | HG02132.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-2870_529-2869d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18886929 | ||||||
| chr17:18886929 | CTTT | C | 145 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(142): Show |
146 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.529-2871_529-2869d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18886929 | ||||||
| chr17:18886929 | CTTTT | C | 7 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0089 others(4): Show |
7 | HG01070.hp2 HG01433.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-2872_529-2869d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18886929 | ||||||
| chr17:18886934 | T | C | 1 | a0001c0003t0003g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.529-2888T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886934 | |||||||
| chr17:18886935 | T | C | 7 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(4): Show |
7 | HG00741.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-2887T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886935 | |||||||
| chr17:18886977 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.529-2845C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886977 | |||||||
| chr17:18886998 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.529-2824G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18886998 | |||||||
| chr17:18887161 | C | A | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.529-2661C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887161 | |||||||
| chr17:18887226 | G | A | 1 | a0001c0002t0002g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529-2596G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887226 | |||||||
| chr17:18887365 | A | G | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.529-2457A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887365 | |||||||
| chr17:18887414 | T | G | 3 | a0001c0001t0006g0191 a0001c0001t0006g0192 a0001c0001t0006g0193 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.529-2408T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887414 | |||||||
| chr17:18887502 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.529-2320T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887502 | |||||||
| chr17:18887519 | G | A | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.529-2303G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887519 | |||||||
| chr17:18887527 | C | A | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.529-2295C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887527 | |||||||
| chr17:18887664 | G | A | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0228 others(2): Show |
5 | HG01891.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-2158G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887664 | |||||||
| chr17:18887792 | C | G | 1 | a0001c0002t0004g0150 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.529-2030C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18887792 | |||||||
| chr17:18887825 | TAACTTGT others(1018): Show |
T | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.529-1981_529-957de others(1): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18887825 | ||||||
| chr17:18887838 | CT | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.529-1970delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18887838 | ||||||
| chr17:18888072 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.529-1750T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888072 | |||||||
| chr17:18888342 | G | T | 20 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0359 others(17): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.529-1480G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888342 | |||||||
| chr17:18888379 | G | T | 1 | a0001c0001t0001g0350 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.529-1443G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888379 | |||||||
| chr17:18888420 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.529-1402C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888420 | |||||||
| chr17:18888465 | C | T | 1 | a0001c0001t0005g0370 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.529-1357C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888465 | |||||||
| chr17:18888479 | A | ACCCCCCA others(299): Show |
1 | a0001c0004t0005g0379 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529-1337_529-1336i others(308): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888479 | ||||||
| chr17:18888498 | G | A | 7 | a0001c0001t0001g0180 a0001c0001t0006g0190 a0001c0001t0006g0191 others(4): Show |
7 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-1324G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888498 | |||||||
| chr17:18888515 | G | A | 3 | a0001c0001t0005g0360 a0001c0001t0005g0365 a0001c0001t0005g0386 |
3 | HG00408.hp2 NA19060.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.529-1307G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888515 | |||||||
| chr17:18888517 | T | G | 1 | a0001c0004t0005g0379 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529-1305T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888517 | |||||||
| chr17:18888544 | C | G | 1 | a0001c0004t0005g0379 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529-1278C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888544 | |||||||
| chr17:18888555 | G | A | 1 | a0001c0004t0005g0379 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529-1267G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888555 | |||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
1 | a0001c0001t0001g0350 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.529-1190_529-1189i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.529-1139_529-1138i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
1 | a0001c0001t0005g0370 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.529-1127_529-1126i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
102 | a0001c0001t0001g0181 a0001c0001t0001g0199 a0001c0001t0001g0205 others(99): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.529-1127_529-1126i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(350): Show |
3 | a0001c0001t0001g0288 a0001c0001t0001g0384 a0001c0001t0005g0364 |
3 | HG03669.hp1 HG04199.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.529-1127_529-1126i others(359): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(348): Show |
73 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0184 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.529-1127_529-1126i others(357): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
1 | a0001c0001t0001g0182 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.529-1127_529-1126i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(350): Show |
4 | a0001c0001t0001g0180 a0001c0001t0001g0207 a0001c0001t0001g0262 others(1): Show |
4 | HG00408.hp1 HG02055.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1127_529-1126i others(359): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
3 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 |
3 | HG02055.hp2 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.529-1127_529-1126i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(348): Show |
1 | a0001c0001t0001g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529-1127_529-1126i others(357): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529-1150_529-1149i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(350): Show |
1 | a0001c0001t0001g0335 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.529-1159_529-1158i others(359): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | NA18947.hp1 NA18949.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.529-1159_529-1158i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(350): Show |
1 | a0001c0001t0001g0349 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.529-1159_529-1158i others(359): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(351): Show |
1 | a0001c0001t0001g0383 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.529-1159_529-1158i others(360): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(350): Show |
1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.529-1171_529-1170i others(359): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | AGGCAGAG others(349): Show |
1 | a0001c0001t0001g0389 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.529-1183_529-1182i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888563 | ||||||
| chr17:18888563 | A | G | 1 | a0001c0004t0005g0379 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529-1259A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888563 | |||||||
| chr17:18888598 | C | CCGGGCAG others(349): Show |
1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.529-1127_529-1126i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888598 | ||||||
| chr17:18888617 | ACCTCCCG others(44): Show |
A | 4 | a0001c0001t0001g0227 a0001c0001t0001g0241 a0001c0001t0001g0243 others(1): Show |
4 | NA18939.hp1 NA18975.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1126_529-1076d others(53): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888617 | ||||||
| chr17:18888633 | G | AGCTGGCC others(349): Show |
5 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(2): Show |
5 | HG00558.hp1 HG01943.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-1190_529-1189i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888633 | |||||||
| chr17:18888655 | A | ACCCCCCC others(350): Show |
1 | a0001c0001t0001g0311 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529-1127_529-1126i others(359): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888655 | ||||||
| chr17:18888663 | C | CACCTCCC others(349): Show |
1 | a0001c0001t0001g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.529-1127_529-1126i others(358): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18888663 | ||||||
| chr17:18888712 | C | G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0237 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1110C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888712 | |||||||
| chr17:18888730 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.529-1092G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888730 | |||||||
| chr17:18888738 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.529-1084T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888738 | |||||||
| chr17:18888938 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.529-884G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888938 | |||||||
| chr17:18888987 | G | C | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.529-835G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18888987 | |||||||
| chr17:18889013 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.529-809G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889013 | |||||||
| chr17:18889043 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.529-779A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889043 | |||||||
| chr17:18889053 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.529-769C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889053 | |||||||
| chr17:18889231 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.529-591T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889231 | |||||||
| chr17:18889349 | AT | A | 4 | a0001c0002t0003g0019 a0001c0002t0003g0025 a0001c0002t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02717.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-466delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 18889349 | ||||||
| chr17:18889406 | G | A | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.529-416G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889406 | |||||||
| chr17:18889417 | G | A | 1 | a0001c0001t0005g0360 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.529-405G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889417 | |||||||
| chr17:18889480 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.529-342C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889480 | |||||||
| chr17:18889748 | C | T | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.529-74C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 7/11 | chr17 | 18889748 | |||||||
| chr17:18889912 | A | G | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.584+35A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18889912 | |||||||
| chr17:18889927 | A | T | 5 | a0001c0002t0002g0158 a0001c0002t0002g0162 a0001c0002t0002g0163 others(2): Show |
5 | HG01192.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.584+50A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18889927 | |||||||
| chr17:18889931 | G | T | 5 | a0001c0002t0002g0158 a0001c0002t0002g0162 a0001c0002t0002g0163 others(2): Show |
5 | HG01192.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.584+54G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18889931 | |||||||
| chr17:18890063 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.584+186C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890063 | |||||||
| chr17:18890104 | C | T | 7 | a0001c0002t0002g0086 a0001c0002t0002g0089 a0001c0002t0002g0093 others(4): Show |
7 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.584+227C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890104 | |||||||
| chr17:18890143 | T | A | 1 | a0001c0002t0002g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.584+266T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890143 | |||||||
| chr17:18890232 | C | T | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | NA18944.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.584+355C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890232 | |||||||
| chr17:18890260 | C | T | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.584+383C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890260 | |||||||
| chr17:18890272 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0333 |
2 | NA18963.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.584+395C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890272 | |||||||
| chr17:18890564 | A | C | 4 | a0001c0002t0003g0019 a0001c0002t0003g0025 a0001c0002t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02717.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+687A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890564 | |||||||
| chr17:18890714 | G | A | 1 | a0001c0002t0002g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.584+837G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890714 | |||||||
| chr17:18890720 | A | C | 1 | a0001c0002t0004g0150 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.584+843A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890720 | |||||||
| chr17:18890729 | G | A | 1 | a0001c0002t0004g0135 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.584+852G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890729 | |||||||
| chr17:18890758 | A | G | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+881A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890758 | |||||||
| chr17:18890794 | AATTG | A | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+921_584+924del others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18890794 | ||||||
| chr17:18890892 | G | T | 2 | a0001c0001t0005g0373 a0001c0001t0005g0374 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.584+1015G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18890892 | |||||||
| chr17:18891055 | T | C | 1 | a0001c0002t0003g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.584+1178T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891055 | |||||||
| chr17:18891284 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.584+1407G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891284 | |||||||
| chr17:18891363 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02886.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.584+1486G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891363 | |||||||
| chr17:18891386 | C | T | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.584+1509C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891386 | |||||||
| chr17:18891603 | C | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.584+1726C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891603 | |||||||
| chr17:18891607 | A | C | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+1730A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891607 | |||||||
| chr17:18891759 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.584+1882G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891759 | |||||||
| chr17:18891984 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.584+2107G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18891984 | |||||||
| chr17:18892004 | A | G | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+2127A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892004 | |||||||
| chr17:18892057 | A | G | 1 | a0001c0001t0001g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.584+2180A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892057 | |||||||
| chr17:18892091 | G | A | 1 | a0001c0002t0003g0015 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.584+2214G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892091 | |||||||
| chr17:18892239 | C | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0278 a0001c0001t0001g0382 |
3 | HG00323.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.584+2362C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892239 | |||||||
| chr17:18892343 | T | C | 8 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+2466T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892343 | |||||||
| chr17:18892465 | A | G | 1 | a0001c0002t0002g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.584+2588A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892465 | |||||||
| chr17:18892512 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0312 |
2 | NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.584+2635A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892512 | |||||||
| chr17:18892666 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.584+2789A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892666 | |||||||
| chr17:18892688 | A | AGT | 27 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(24): Show |
27 | HG00558.hp1 HG01346.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.584+2850_584+2851d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892688 | ||||||
| chr17:18892688 | A | AGTGT | 34 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0206 others(31): Show |
35 | HG01256.hp2 HG01934.hp2 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.584+2848_584+2851d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892688 | ||||||
| chr17:18892688 | A | AGTGTGT | 20 | a0001c0001t0001g0185 a0001c0001t0001g0198 a0001c0001t0001g0200 others(17): Show |
20 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.584+2846_584+2851d others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892688 | ||||||
| chr17:18892688 | A | AGTGTGTG others(1): Show |
49 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(46): Show |
49 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.584+2844_584+2851d others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892688 | ||||||
| chr17:18892688 | A | AGTGTGTG others(3): Show |
28 | a0001c0001t0001g0187 a0001c0001t0001g0199 a0001c0001t0001g0213 others(25): Show |
28 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+2842_584+2851d others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892688 | ||||||
| chr17:18892688 | A | AGTGTGTG others(5): Show |
7 | a0001c0001t0001g0196 a0001c0001t0001g0203 a0001c0001t0001g0204 others(4): Show |
7 | HG01891.hp1 HG02027.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+2840_584+2851d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892688 | ||||||
| chr17:18892719 | G | T | 2 | a0001c0002t0002g0107 a0001c0002t0002g0168 |
2 | HG04199.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.584+2842G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892719 | |||||||
| chr17:18892721 | G | A | 2 | a0001c0002t0002g0107 a0001c0002t0002g0168 |
2 | HG04199.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.584+2844G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892721 | |||||||
| chr17:18892723 | G | T | 4 | a0001c0002t0002g0107 a0001c0002t0002g0160 a0001c0002t0002g0161 others(1): Show |
4 | HG02132.hp1 HG04199.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+2846G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892723 | |||||||
| chr17:18892725 | G | A | 6 | a0001c0002t0002g0048 a0001c0002t0002g0055 a0001c0002t0002g0107 others(3): Show |
6 | HG02132.hp1 HG03139.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.584+2848G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892725 | |||||||
| chr17:18892727 | G | GTGTGTGT others(27): Show |
1 | a0001c0002t0002g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.584+2851_584+2852i others(36): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(19): Show |
1 | a0001c0002t0002g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.584+2851_584+2852i others(28): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(17): Show |
8 | a0001c0002t0002g0032 a0001c0002t0002g0069 a0001c0002t0002g0070 others(5): Show |
8 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(26): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(14): Show |
2 | a0001c0002t0002g0067 a0001c0002t0002g0111 |
2 | HG01192.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.584+2851_584+2852i others(23): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(15): Show |
20 | a0001c0002t0002g0037 a0001c0002t0002g0043 a0001c0002t0002g0051 others(17): Show |
20 | HG00323.hp2 HG00423.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(24): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(5): Show |
1 | a0001c0002t0003g0013 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.584+2851_584+2852i others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(9): Show |
1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.584+2851_584+2852i others(18): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(13): Show |
34 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 others(31): Show |
34 | HG00558.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(22): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(17): Show |
1 | a0001c0002t0002g0079 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.584+2851_584+2852i others(26): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(3): Show |
7 | a0001c0002t0004g0131 a0001c0002t0004g0133 a0001c0002t0004g0135 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(10): Show |
1 | a0001c0002t0002g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.584+2851_584+2852i others(19): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(11): Show |
14 | a0001c0002t0002g0036 a0001c0002t0002g0050 a0001c0002t0002g0053 others(11): Show |
14 | HG00733.hp2 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(1): Show |
9 | a0001c0002t0003g0024 a0001c0002t0004g0127 a0001c0002t0004g0130 others(6): Show |
9 | HG01106.hp2 HG01433.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTGT others(9): Show |
19 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0044 others(16): Show |
20 | HG01069.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(18): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTT | 7 | a0001c0002t0003g0015 a0001c0002t0003g0020 a0001c0002t0003g0023 others(4): Show |
7 | HG00140.hp2 HG00642.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTGTGTTT others(7): Show |
6 | a0001c0001t0002g0171 a0001c0002t0002g0165 a0001c0002t0002g0170 others(3): Show |
6 | HG01361.hp2 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTT | 7 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(4): Show |
7 | HG00741.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | GTTTATTT others(3): Show |
6 | a0001c0002t0002g0152 a0001c0002t0002g0154 a0001c0002t0002g0155 others(3): Show |
6 | HG01433.hp2 HG02572.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+2851_584+2852i others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892727 | ||||||
| chr17:18892727 | G | T | 8 | a0001c0002t0002g0004 a0001c0002t0002g0048 a0001c0002t0002g0055 others(5): Show |
8 | HG02132.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+2850G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892727 | |||||||
| chr17:18892729 | A | G | 15 | a0001c0002t0002g0153 a0001c0002t0002g0157 a0001c0002t0002g0158 others(12): Show |
15 | HG00738.hp1 HG01168.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.584+2852A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892729 | |||||||
| chr17:18892741 | A | ATTTTT | 8 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+2867_584+2868i others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892741 | ||||||
| chr17:18892745 | A | AT | 110 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(107): Show |
111 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.584+2875dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892745 | ||||||
| chr17:18892745 | A | ATTTATTT others(6): Show |
9 | a0001c0002t0002g0153 a0001c0002t0002g0157 a0001c0002t0002g0158 others(6): Show |
9 | HG01192.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.584+2871_584+2872i others(15): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892745 | ||||||
| chr17:18892745 | A | ATTTATTT others(3): Show |
1 | a0001c0002t0003g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.584+2871_584+2872i others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892745 | ||||||
| chr17:18892745 | A | ATTTATTT others(5): Show |
2 | a0001c0002t0004g0132 a0001c0002t0004g0148 |
2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.584+2871_584+2872i others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892745 | ||||||
| chr17:18892745 | A | ATTTTT | 17 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0003g0013 others(14): Show |
17 | HG00642.hp2 HG01123.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.584+2871_584+2875d others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892745 | ||||||
| chr17:18892745 | A | ATTTTTTT others(1): Show |
16 | a0001c0002t0004g0127 a0001c0002t0004g0129 a0001c0002t0004g0130 others(13): Show |
16 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.584+2875_584+2876i others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18892745 | ||||||
| chr17:18892745 | A | T | 17 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0004g0128 others(14): Show |
17 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.584+2868A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892745 | |||||||
| chr17:18892795 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0221 a0001c0001t0001g0260 others(3): Show |
7 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+2918C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892795 | |||||||
| chr17:18892984 | G | A | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+3107G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18892984 | |||||||
| chr17:18893088 | T | G | 3 | a0001c0002t0003g0023 a0001c0002t0003g0024 a0001c0002t0003g0030 |
3 | HG01934.hp1 HG01993.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.584+3211T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893088 | |||||||
| chr17:18893133 | G | T | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+3256G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893133 | |||||||
| chr17:18893153 | CT | C | 26 | a0001c0001t0001g0270 a0001c0001t0001g0336 a0001c0001t0001g0351 others(23): Show |
26 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.584+3295delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18893153 | ||||||
| chr17:18893153 | CTT | C | 21 | a0001c0001t0005g0359 a0001c0002t0002g0003 a0001c0002t0002g0004 others(18): Show |
21 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.584+3294_584+3295d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18893153 | ||||||
| chr17:18893153 | CTTT | C | 153 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(150): Show |
154 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.584+3293_584+3295d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18893153 | ||||||
| chr17:18893177 | C | T | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+3300C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893177 | |||||||
| chr17:18893297 | C | T | 1 | a0001c0002t0002g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.584+3420C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893297 | |||||||
| chr17:18893385 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.584+3508G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893385 | |||||||
| chr17:18893478 | G | T | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+3601G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893478 | |||||||
| chr17:18893584 | G | A | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+3707G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893584 | |||||||
| chr17:18893592 | G | GA | 153 | a0001c0001t0001g0302 a0001c0001t0002g0171 a0001c0001t0006g0190 others(150): Show |
154 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.584+3726dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18893592 | ||||||
| chr17:18893592 | G | GAA | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.584+3725_584+3726d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18893592 | ||||||
| chr17:18893599 | A | T | 1 | a0001c0002t0002g0047 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.584+3722A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893599 | |||||||
| chr17:18893602 | A | AT | 9 | a0001c0002t0003g0028 a0001c0003t0003g0005 a0001c0003t0003g0006 others(6): Show |
9 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+3725_584+3726i others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893602 | |||||||
| chr17:18893718 | G | A | 9 | a0001c0002t0003g0028 a0001c0003t0003g0005 a0001c0003t0003g0006 others(6): Show |
9 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+3841G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893718 | |||||||
| chr17:18893727 | AT | A | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+3855delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18893727 | ||||||
| chr17:18893813 | A | G | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+3936A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893813 | |||||||
| chr17:18893853 | C | T | 2 | a0001c0001t0001g0299 a0001c0002t0009g0179 |
2 | HG02132.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.584+3976C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893853 | |||||||
| chr17:18893867 | A | G | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+3990A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18893867 | |||||||
| chr17:18894014 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.584+4137C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894014 | |||||||
| chr17:18894024 | A | G | 121 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(118): Show |
122 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.584+4147A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894024 | |||||||
| chr17:18894180 | G | A | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.584+4303G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894180 | |||||||
| chr17:18894308 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0381 |
2 | HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.584+4431C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894308 | |||||||
| chr17:18894316 | C | T | 12 | a0001c0002t0002g0058 a0001c0002t0002g0060 a0001c0002t0002g0074 others(9): Show |
12 | HG00423.hp2 HG00544.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.584+4439C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894316 | |||||||
| chr17:18894454 | C | T | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+4577C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894454 | |||||||
| chr17:18894479 | C | CT | 44 | a0001c0001t0001g0180 a0001c0001t0001g0269 a0001c0001t0001g0283 others(41): Show |
44 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.584+4620dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18894479 | ||||||
| chr17:18894479 | C | CTTTTTTT others(3): Show |
8 | a0001c0002t0002g0003 a0001c0002t0004g0142 a0001c0003t0003g0007 others(5): Show |
8 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+4611_584+4620d others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18894479 | ||||||
| chr17:18894479 | C | CTTTTTTT others(4): Show |
36 | a0001c0002t0002g0004 a0001c0002t0003g0013 a0001c0002t0003g0014 others(33): Show |
36 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.584+4610_584+4620d others(13): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18894479 | ||||||
| chr17:18894479 | C | CTTTTTTT others(5): Show |
8 | a0001c0002t0003g0025 a0001c0002t0003g0026 a0001c0002t0003g0027 others(5): Show |
8 | HG01243.hp2 HG01361.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+4609_584+4620d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18894479 | ||||||
| chr17:18894612 | G | A | 2 | a0001c0002t0002g0059 a0001c0002t0002g0101 |
2 | NA18984.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.584+4735G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894612 | |||||||
| chr17:18894719 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.584+4842G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894719 | |||||||
| chr17:18894734 | C | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.584+4857C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894734 | |||||||
| chr17:18894763 | G | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.584+4886G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18894763 | |||||||
| chr17:18895013 | C | A | 1 | a0001c0002t0004g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.584+5136C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895013 | |||||||
| chr17:18895081 | C | CT | 9 | a0001c0001t0001g0275 a0001c0001t0001g0296 a0001c0001t0001g0298 others(6): Show |
9 | HG01981.hp1 HG02055.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.584+5223dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18895081 | ||||||
| chr17:18895081 | CT | C | 157 | a0001c0001t0001g0213 a0001c0001t0001g0316 a0001c0001t0001g0325 others(154): Show |
158 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.584+5223delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18895081 | ||||||
| chr17:18895081 | CTT | C | 24 | a0001c0002t0002g0059 a0001c0002t0002g0063 a0001c0002t0004g0131 others(21): Show |
24 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.584+5222_584+5223d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18895081 | ||||||
| chr17:18895142 | T | C | 4 | a0001c0002t0002g0073 a0001c0002t0002g0090 a0001c0002t0002g0113 others(1): Show |
4 | HG02572.hp2 HG02895.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+5265T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895142 | |||||||
| chr17:18895260 | A | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0181 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.584+5383A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895260 | |||||||
| chr17:18895262 | T | A | 26 | a0001c0002t0002g0032 a0001c0002t0002g0084 a0001c0002t0002g0096 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+5385T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895262 | |||||||
| chr17:18895271 | A | T | 1 | a0001c0002t0002g0053 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.584+5394A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895271 | |||||||
| chr17:18895280 | T | C | 121 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(118): Show |
122 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.584+5403T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895280 | |||||||
| chr17:18895287 | G | A | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+5410G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895287 | |||||||
| chr17:18895533 | T | G | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+5656T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895533 | |||||||
| chr17:18895699 | C | T | 17 | a0001c0001t0002g0171 a0001c0002t0002g0152 a0001c0002t0002g0157 others(14): Show |
17 | HG01891.hp2 HG02132.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.584+5822C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895699 | |||||||
| chr17:18895729 | G | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0308 |
2 | NA18964.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.584+5852G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895729 | |||||||
| chr17:18895943 | A | G | 1 | a0001c0002t0002g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.584+6066A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18895943 | |||||||
| chr17:18896069 | C | A | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0320 |
3 | NA18954.hp2 NA18981.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.584+6192C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896069 | |||||||
| chr17:18896210 | T | C | 9 | a0001c0002t0003g0028 a0001c0003t0003g0005 a0001c0003t0003g0006 others(6): Show |
9 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+6333T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896210 | |||||||
| chr17:18896361 | C | T | 1 | a0001c0002t0002g0153 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.584+6484C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896361 | |||||||
| chr17:18896401 | A | G | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+6524A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896401 | |||||||
| chr17:18896580 | C | CT | 170 | a0001c0001t0001g0224 a0001c0001t0001g0249 a0001c0001t0001g0268 others(167): Show |
171 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.584+6723dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18896580 | ||||||
| chr17:18896580 | C | CTT | 28 | a0001c0001t0001g0264 a0001c0001t0005g0359 a0001c0001t0005g0373 others(25): Show |
28 | HG00140.hp2 HG00323.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.584+6722_584+6723d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18896580 | ||||||
| chr17:18896581 | T | C | 1 | a0001c0001t0001g0388 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.584+6704T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896581 | |||||||
| chr17:18896629 | A | G | 1 | a0001c0002t0002g0103 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.584+6752A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896629 | |||||||
| chr17:18896643 | C | T | 26 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+6766C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896643 | |||||||
| chr17:18896763 | A | T | 1 | a0001c0002t0002g0120 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.584+6886A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896763 | |||||||
| chr17:18896779 | T | C | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+6902T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896779 | |||||||
| chr17:18896905 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0221 a0001c0001t0001g0260 others(2): Show |
6 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.584+7028T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18896905 | |||||||
| chr17:18896969 | C | CT | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+7100dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18896969 | ||||||
| chr17:18897036 | T | G | 1 | a0001c0002t0002g0082 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.584+7159T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897036 | |||||||
| chr17:18897173 | G | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0277 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.584+7296G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897173 | |||||||
| chr17:18897257 | C | T | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.584+7380C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897257 | |||||||
| chr17:18897450 | G | GTGTTGT | 7 | a0001c0002t0002g0089 a0001c0002t0002g0093 a0001c0002t0002g0099 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+7575_584+7576i others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897450 | ||||||
| chr17:18897450 | G | GTGTTGTT others(2): Show |
3 | a0001c0002t0002g0042 a0001c0002t0002g0072 a0001c0002t0002g0153 |
3 | HG02015.hp1 HG02293.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.584+7575_584+7576i others(11): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897450 | ||||||
| chr17:18897450 | G | GTGTTGTT others(5): Show |
81 | a0001c0002t0002g0001 a0001c0002t0002g0032 a0001c0002t0002g0035 others(78): Show |
82 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.584+7575_584+7576i others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897450 | ||||||
| chr17:18897450 | G | GTGTTGTT others(8): Show |
13 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0058 others(10): Show |
13 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.584+7575_584+7576i others(17): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897450 | ||||||
| chr17:18897450 | G | GTGTTGTT others(11): Show |
12 | a0001c0001t0002g0171 a0001c0002t0002g0054 a0001c0002t0002g0065 others(9): Show |
12 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.584+7575_584+7576i others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897450 | ||||||
| chr17:18897450 | G | GTGTTGTT others(14): Show |
1 | a0001c0002t0002g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.584+7575_584+7576i others(23): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897450 | ||||||
| chr17:18897453 | G | GTGTTGT | 27 | a0001c0002t0002g0004 a0001c0002t0003g0013 a0001c0002t0003g0014 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.584+7596_584+7601d others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897453 | ||||||
| chr17:18897453 | G | GTGTTGTT others(2): Show |
6 | a0001c0002t0002g0003 a0001c0002t0004g0127 a0001c0002t0004g0128 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+7593_584+7601d others(11): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897453 | ||||||
| chr17:18897453 | G | GTGTTGTT others(5): Show |
22 | a0001c0002t0004g0131 a0001c0002t0004g0132 a0001c0002t0004g0133 others(19): Show |
22 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.584+7590_584+7601d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897453 | ||||||
| chr17:18897453 | G | GTGTTGTT others(11): Show |
2 | a0001c0002t0002g0154 a0001c0002t0002g0156 |
2 | HG01433.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.584+7584_584+7601d others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897453 | ||||||
| chr17:18897453 | G | GTGTTGTT others(14): Show |
1 | a0001c0002t0002g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.584+7581_584+7601d others(23): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897453 | ||||||
| chr17:18897453 | G | T | 118 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(115): Show |
119 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.584+7576G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897453 | |||||||
| chr17:18897483 | C | T | 1 | a0001c0002t0004g0150 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.584+7606C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897483 | |||||||
| chr17:18897585 | C | G | 1 | a0001c0002t0002g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.584+7708C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897585 | |||||||
| chr17:18897651 | G | A | 2 | a0001c0001t0005g0373 a0001c0001t0005g0374 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.584+7774G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897651 | |||||||
| chr17:18897755 | G | A | 1 | a0001c0001t0005g0364 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.584+7878G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897755 | |||||||
| chr17:18897951 | T | C | 1 | a0001c0001t0001g0389 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.584+8074T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897951 | |||||||
| chr17:18897962 | A | G | 1 | a0001c0002t0002g0153 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.584+8085A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897962 | |||||||
| chr17:18897965 | G | A | 1 | a0001c0002t0002g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.584+8088G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18897965 | |||||||
| chr17:18897991 | C | CT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(104): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.584+8140dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897991 | ||||||
| chr17:18897991 | C | CTT | 18 | a0001c0001t0001g0188 a0001c0001t0001g0201 a0001c0001t0001g0222 others(15): Show |
18 | HG00423.hp1 HG01981.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.584+8139_584+8140d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897991 | ||||||
| chr17:18897991 | CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0004g0136 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.584+8128_584+8140d others(15): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897991 | ||||||
| chr17:18897991 | CTTTTTTT others(7): Show |
C | 175 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(172): Show |
176 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.584+8127_584+8140d others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18897991 | ||||||
| chr17:18898067 | T | C | 184 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0002g0171 others(181): Show |
185 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.584+8190T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898067 | |||||||
| chr17:18898190 | G | C | 1 | a0001c0001t0001g0325 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.584+8313G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898190 | |||||||
| chr17:18898249 | G | A | 1 | a0001c0001t0005g0360 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.584+8372G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898249 | |||||||
| chr17:18898496 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.584+8619C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898496 | |||||||
| chr17:18898528 | A | G | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+8651A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898528 | |||||||
| chr17:18898571 | C | T | 1 | a0001c0002t0004g0151 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.584+8694C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898571 | |||||||
| chr17:18898715 | C | A | 57 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.584+8838C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898715 | |||||||
| chr17:18898885 | GTGTT | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0181 a0001c0001t0001g0182 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.584+9039_584+9042d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18898885 | ||||||
| chr17:18898885 | GTGTTTGT others(1): Show |
G | 156 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0171 others(153): Show |
157 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.584+9035_584+9042d others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18898885 | ||||||
| chr17:18898885 | GTGTTTGT others(5): Show |
G | 1 | a0001c0001t0002g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.584+9031_584+9042d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18898885 | ||||||
| chr17:18898958 | A | G | 1 | a0001c0002t0008g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.584+9081A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898958 | |||||||
| chr17:18898963 | G | A | 2 | a0001c0001t0005g0365 a0001c0001t0005g0386 |
2 | NA19060.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.584+9086G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18898963 | |||||||
| chr17:18899037 | T | G | 1 | a0001c0002t0003g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.584+9160T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899037 | |||||||
| chr17:18899228 | A | G | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+9351A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899228 | |||||||
| chr17:18899368 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0381 |
2 | HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.584+9491A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899368 | |||||||
| chr17:18899385 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02886.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.584+9508C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899385 | |||||||
| chr17:18899519 | G | GT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0203 others(33): Show |
37 | HG00423.hp1 HG02027.hp1 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.584+9668dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18899519 | ||||||
| chr17:18899519 | G | GTT | 11 | a0001c0001t0001g0198 a0001c0001t0001g0201 a0001c0001t0001g0220 others(8): Show |
11 | HG01071.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.584+9667_584+9668d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18899519 | ||||||
| chr17:18899519 | G | GTTT | 46 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0186 others(43): Show |
46 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.584+9666_584+9668d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18899519 | ||||||
| chr17:18899519 | G | GTTTT | 13 | a0001c0001t0001g0184 a0001c0001t0001g0235 a0001c0001t0001g0238 others(10): Show |
13 | HG00140.hp1 HG01106.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.584+9665_584+9668d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18899519 | ||||||
| chr17:18899519 | GT | G | 92 | a0001c0001t0001g0272 a0001c0001t0002g0171 a0001c0001t0005g0377 others(89): Show |
93 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.584+9668delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18899519 | ||||||
| chr17:18899519 | GTT | G | 73 | a0001c0001t0006g0192 a0001c0002t0002g0003 a0001c0002t0002g0004 others(70): Show |
73 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.584+9667_584+9668d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18899519 | ||||||
| chr17:18899520 | T | G | 2 | a0001c0001t0001g0313 a0001c0001t0001g0320 |
2 | NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.584+9643T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899520 | |||||||
| chr17:18899544 | T | G | 8 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(5): Show |
8 | HG00558.hp2 HG02015.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+9667T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899544 | |||||||
| chr17:18899647 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.584+9770G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899647 | |||||||
| chr17:18899811 | C | T | 22 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0359 others(19): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.584+9934C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899811 | |||||||
| chr17:18899831 | C | T | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+9954C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899831 | |||||||
| chr17:18899948 | G | C | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.584+10071G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899948 | |||||||
| chr17:18899972 | C | T | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+10095C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18899972 | |||||||
| chr17:18900047 | C | T | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+10170C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900047 | |||||||
| chr17:18900140 | C | T | 1 | a0001c0004t0005g0379 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.584+10263C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900140 | |||||||
| chr17:18900146 | G | A | 176 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0003 others(173): Show |
177 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.584+10269G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900146 | |||||||
| chr17:18900213 | G | T | 1 | a0001c0001t0001g0389 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.584+10336G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900213 | |||||||
| chr17:18900273 | C | T | 8 | a0001c0001t0001g0180 a0001c0001t0001g0388 a0001c0001t0006g0190 others(5): Show |
8 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.584+10396C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900273 | |||||||
| chr17:18900314 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.584+10437G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900314 | |||||||
| chr17:18900345 | A | G | 129 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(126): Show |
130 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.584+10468A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900345 | |||||||
| chr17:18900437 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.584+10560C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900437 | |||||||
| chr17:18900454 | T | C | 1 | a0001c0002t0002g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.584+10577T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900454 | |||||||
| chr17:18900482 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.584+10605T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900482 | |||||||
| chr17:18900668 | C | T | 35 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(32): Show |
35 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.585-10435C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900668 | |||||||
| chr17:18900710 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.585-10393G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900710 | |||||||
| chr17:18900759 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.585-10344G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900759 | |||||||
| chr17:18900782 | C | T | 1 | a0001c0002t0004g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.585-10321C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900782 | |||||||
| chr17:18900822 | G | A | 98 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0199 others(95): Show |
98 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.585-10281G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900822 | |||||||
| chr17:18900886 | T | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.585-10217T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900886 | |||||||
| chr17:18900904 | A | G | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.585-10199A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18900904 | |||||||
| chr17:18901056 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.585-10047C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901056 | |||||||
| chr17:18901072 | T | C | 147 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(144): Show |
148 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.585-10031T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901072 | |||||||
| chr17:18901100 | C | T | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-10003C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901100 | |||||||
| chr17:18901132 | G | C | 1 | a0001c0001t0001g0341 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.585-9971G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901132 | |||||||
| chr17:18901197 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.585-9906C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901197 | |||||||
| chr17:18901233 | C | T | 1 | a0001c0002t0002g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.585-9870C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901233 | |||||||
| chr17:18901321 | C | T | 1 | a0001c0002t0002g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.585-9782C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901321 | |||||||
| chr17:18901419 | A | G | 1 | a0001c0002t0002g0036 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.585-9684A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901419 | |||||||
| chr17:18901633 | C | T | 2 | a0001c0001t0005g0373 a0001c0001t0005g0374 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.585-9470C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901633 | |||||||
| chr17:18901977 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.585-9126T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18901977 | |||||||
| chr17:18902108 | A | G | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.585-8995A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902108 | |||||||
| chr17:18902150 | C | T | 1 | a0001c0002t0002g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.585-8953C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902150 | |||||||
| chr17:18902207 | C | G | 61 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(58): Show |
61 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.585-8896C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902207 | |||||||
| chr17:18902234 | C | A | 4 | a0001c0002t0003g0019 a0001c0002t0003g0025 a0001c0002t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02717.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.585-8869C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902234 | |||||||
| chr17:18902470 | C | T | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585-8633C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902470 | |||||||
| chr17:18902487 | ATGT | A | 11 | a0001c0001t0002g0171 a0001c0002t0002g0164 a0001c0002t0002g0165 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.585-8611_585-8609d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18902487 | ||||||
| chr17:18902574 | A | G | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-8529A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902574 | |||||||
| chr17:18902712 | A | T | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-8391A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902712 | |||||||
| chr17:18902738 | G | A | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.585-8365G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902738 | |||||||
| chr17:18902738 | G | T | 4 | a0001c0002t0003g0019 a0001c0002t0003g0025 a0001c0002t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02717.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.585-8365G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902738 | |||||||
| chr17:18902826 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.585-8277G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902826 | |||||||
| chr17:18902869 | C | CA | 10 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0209 others(7): Show |
10 | HG01175.hp2 HG02300.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.585-8210dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18902869 | ||||||
| chr17:18902869 | CA | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0237 others(10): Show |
14 | HG00323.hp1 HG02451.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.585-8210delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18902869 | ||||||
| chr17:18902869 | CAA | C | 55 | a0001c0001t0001g0357 a0001c0001t0006g0190 a0001c0001t0006g0192 others(52): Show |
55 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.585-8211_585-8210d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18902869 | ||||||
| chr17:18902869 | CAAA | C | 119 | a0001c0001t0002g0171 a0001c0001t0006g0191 a0001c0002t0002g0001 others(116): Show |
120 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.585-8212_585-8210d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18902869 | ||||||
| chr17:18902890 | A | G | 1 | a0001c0001t0001g0339 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.585-8213A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902890 | |||||||
| chr17:18902893 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.585-8210A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902893 | |||||||
| chr17:18902896 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.585-8207A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902896 | |||||||
| chr17:18902924 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.585-8179T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18902924 | |||||||
| chr17:18903166 | CCCTGTAA others(299): Show |
C | 3 | a0001c0002t0002g0154 a0001c0002t0002g0155 a0001c0002t0002g0156 |
3 | HG01433.hp2 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.585-7910_585-7605d others(2): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18903166 | ||||||
| chr17:18903386 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0312 |
2 | NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.585-7717A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18903386 | |||||||
| chr17:18903593 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.585-7510G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18903593 | |||||||
| chr17:18903748 | A | G | 1 | a0001c0002t0002g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.585-7355A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18903748 | |||||||
| chr17:18903765 | G | A | 67 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.585-7338G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18903765 | |||||||
| chr17:18903818 | T | C | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-7285T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18903818 | |||||||
| chr17:18904134 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.585-6969C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18904134 | |||||||
| chr17:18904293 | C | T | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.585-6810C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18904293 | |||||||
| chr17:18904571 | T | C | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-6532T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18904571 | |||||||
| chr17:18904626 | C | G | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-6477C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18904626 | |||||||
| chr17:18904814 | A | T | 2 | a0001c0002t0002g0048 a0001c0002t0002g0055 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.585-6289A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18904814 | |||||||
| chr17:18905063 | G | A | 1 | a0001c0001t0001g0347 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.585-6040G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905063 | |||||||
| chr17:18905148 | C | G | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | NA18959.hp2 NA18964.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.585-5955C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905148 | |||||||
| chr17:18905170 | C | G | 7 | a0001c0002t0002g0062 a0001c0002t0002g0087 a0001c0002t0002g0091 others(4): Show |
7 | HG01952.hp2 HG03654.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.585-5933C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905170 | |||||||
| chr17:18905214 | C | T | 3 | a0001c0002t0002g0154 a0001c0002t0002g0155 a0001c0002t0002g0156 |
3 | HG01433.hp2 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.585-5889C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905214 | |||||||
| chr17:18905582 | AT | A | 11 | a0001c0001t0001g0303 a0001c0001t0001g0342 a0001c0002t0002g0152 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.585-5507delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18905582 | ||||||
| chr17:18905591 | T | C | 7 | a0001c0002t0002g0062 a0001c0002t0002g0087 a0001c0002t0002g0091 others(4): Show |
7 | HG01952.hp2 HG03654.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.585-5512T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905591 | |||||||
| chr17:18905601 | C | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0249 a0001c0001t0001g0264 others(1): Show |
4 | HG01175.hp2 HG01256.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.585-5502C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905601 | |||||||
| chr17:18905610 | G | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585-5493G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905610 | |||||||
| chr17:18905655 | C | T | 2 | a0001c0002t0004g0127 a0001c0002t0004g0128 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.585-5448C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905655 | |||||||
| chr17:18905679 | A | C | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.585-5424A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905679 | |||||||
| chr17:18905703 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.585-5400C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905703 | |||||||
| chr17:18905887 | T | C | 1 | a0001c0002t0002g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.585-5216T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905887 | |||||||
| chr17:18905955 | A | G | 67 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.585-5148A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18905955 | |||||||
| chr17:18906191 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG02074.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.585-4912C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906191 | |||||||
| chr17:18906200 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.585-4903G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906200 | |||||||
| chr17:18906203 | A | ATTGT | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.585-4877_585-4874d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18906203 | ||||||
| chr17:18906218 | GTTTGTTT others(5): Show |
G | 1 | a0001c0001t0006g0190 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.585-4880_585-4869d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18906218 | ||||||
| chr17:18906230 | A | G | 182 | a0001c0001t0001g0355 a0001c0001t0002g0171 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-4873A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906230 | |||||||
| chr17:18906451 | C | T | 58 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.585-4652C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906451 | |||||||
| chr17:18906461 | G | C | 1 | a0001c0001t0001g0322 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.585-4642G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906461 | |||||||
| chr17:18906462 | C | G | 1 | a0001c0001t0001g0322 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.585-4641C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906462 | |||||||
| chr17:18906581 | C | G | 1 | a0001c0001t0001g0348 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.585-4522C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906581 | |||||||
| chr17:18906689 | G | A | 181 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(178): Show |
182 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.585-4414G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906689 | |||||||
| chr17:18906689 | G | T | 1 | a0001c0002t0002g0038 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.585-4414G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906689 | |||||||
| chr17:18906872 | C | G | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.585-4231C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18906872 | |||||||
| chr17:18907050 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.585-4053G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18907050 | |||||||
| chr17:18907106 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.585-3997A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18907106 | |||||||
| chr17:18907283 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.585-3820C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18907283 | |||||||
| chr17:18907336 | G | A | 1 | a0001c0002t0002g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.585-3767G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18907336 | |||||||
| chr17:18907771 | A | G | 1 | a0001c0002t0002g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585-3332A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18907771 | |||||||
| chr17:18907804 | G | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585-3299G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18907804 | |||||||
| chr17:18907863 | G | A | 3 | a0001c0001t0005g0373 a0001c0001t0005g0374 a0001c0002t0003g0028 |
3 | HG03041.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.585-3240G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18907863 | |||||||
| chr17:18908023 | A | G | 1 | a0001c0002t0002g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.585-3080A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908023 | |||||||
| chr17:18908164 | C | CA | 120 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(117): Show |
121 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.585-2931dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18908164 | ||||||
| chr17:18908166 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.585-2937A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908166 | |||||||
| chr17:18908188 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.585-2915A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908188 | |||||||
| chr17:18908334 | A | G | 2 | a0001c0002t0002g0047 a0001c0002t0002g0050 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.585-2769A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908334 | |||||||
| chr17:18908389 | A | G | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-2714A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908389 | |||||||
| chr17:18908533 | C | T | 121 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(118): Show |
122 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.585-2570C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908533 | |||||||
| chr17:18908606 | T | C | 1 | a0001c0002t0004g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.585-2497T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908606 | |||||||
| chr17:18908789 | CA | C | 182 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(179): Show |
183 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.585-2307delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18908789 | ||||||
| chr17:18908905 | T | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.585-2198T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18908905 | |||||||
| chr17:18909240 | C | CT | 9 | a0001c0001t0001g0296 a0001c0001t0001g0306 a0001c0001t0001g0310 others(6): Show |
9 | HG01981.hp2 HG02074.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.585-1844dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18909240 | ||||||
| chr17:18909240 | CT | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0184 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.585-1844delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 18909240 | ||||||
| chr17:18909273 | G | A | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.585-1830G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909273 | |||||||
| chr17:18909394 | A | C | 1 | a0001c0002t0002g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.585-1709A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909394 | |||||||
| chr17:18909403 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0356 a0001c0001t0001g0357 |
4 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.585-1700G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909403 | |||||||
| chr17:18909539 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG03471.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.585-1564C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909539 | |||||||
| chr17:18909643 | A | G | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.585-1460A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909643 | |||||||
| chr17:18909775 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.585-1328C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909775 | |||||||
| chr17:18909776 | G | A | 1 | a0001c0002t0003g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.585-1327G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909776 | |||||||
| chr17:18909776 | G | T | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.585-1327G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909776 | |||||||
| chr17:18909847 | A | G | 183 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0235 others(180): Show |
184 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.585-1256A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18909847 | |||||||
| chr17:18910050 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.585-1053T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18910050 | |||||||
| chr17:18910119 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.585-984C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18910119 | |||||||
| chr17:18910529 | A | C | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.585-574A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18910529 | |||||||
| chr17:18910531 | C | G | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.585-572C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18910531 | |||||||
| chr17:18910532 | ACTT | A | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.585-570_585-568del others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18910532 | |||||||
| chr17:18910537 | GT | G | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.585-565delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18910537 | |||||||
| chr17:18910676 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.585-427T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 8/11 | chr17 | 18910676 | |||||||
| chr17:18911265 | TG | T | 3 | a0001c0002t0002g0032 a0001c0002t0002g0084 a0001c0002t0002g0119 |
3 | HG03831.hp2 HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.733+15delG | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18911265 | |||||||
| chr17:18911348 | T | TTA | 292 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.733+97_733+98insTA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18911348 | |||||||
| chr17:18911397 | G | A | 1 | a0001c0001t0005g0368 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.733+146G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18911397 | |||||||
| chr17:18911517 | T | C | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+266T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18911517 | |||||||
| chr17:18911589 | G | A | 1 | a0001c0003t0003g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.733+338G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18911589 | |||||||
| chr17:18911592 | ATGT | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(105): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.733+346_733+348del others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18911592 | ||||||
| chr17:18911595 | T | A | 4 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+344T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18911595 | |||||||
| chr17:18911663 | C | T | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+412C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18911663 | |||||||
| chr17:18912096 | C | A | 4 | a0001c0002t0003g0019 a0001c0002t0003g0025 a0001c0002t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02717.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+845C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912096 | |||||||
| chr17:18912205 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0264 |
2 | HG01175.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.733+954G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912205 | |||||||
| chr17:18912233 | C | T | 2 | a0001c0002t0003g0018 a0001c0002t0003g0020 |
2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.733+982C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912233 | |||||||
| chr17:18912234 | T | G | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+983T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912234 | |||||||
| chr17:18912325 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.733+1074C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912325 | |||||||
| chr17:18912550 | C | A | 1 | a0001c0002t0002g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.733+1299C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912550 | |||||||
| chr17:18912651 | C | T | 4 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | NA18983.hp1 NA18988.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+1400C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912651 | |||||||
| chr17:18912946 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.733+1695C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912946 | |||||||
| chr17:18912961 | C | T | 22 | a0001c0002t0004g0131 a0001c0002t0004g0132 a0001c0002t0004g0133 others(19): Show |
22 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.733+1710C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18912961 | |||||||
| chr17:18913145 | G | A | 1 | a0001c0002t0002g0157 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733+1894G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913145 | |||||||
| chr17:18913353 | A | G | 1 | a0001c0002t0002g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.733+2102A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913353 | |||||||
| chr17:18913427 | G | A | 121 | a0001c0001t0002g0171 a0001c0002t0002g0001 a0001c0002t0002g0032 others(118): Show |
122 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.733+2176G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913427 | |||||||
| chr17:18913427 | G | T | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.733+2176G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913427 | |||||||
| chr17:18913532 | C | G | 1 | a0001c0001t0001g0322 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733+2281C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913532 | |||||||
| chr17:18913533 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.733+2282G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913533 | |||||||
| chr17:18913541 | C | CT | 69 | a0001c0001t0001g0199 a0001c0001t0001g0205 a0001c0001t0001g0215 others(66): Show |
69 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.733+2315dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18913541 | ||||||
| chr17:18913541 | C | CTT | 31 | a0001c0001t0001g0269 a0001c0001t0001g0275 a0001c0001t0001g0318 others(28): Show |
31 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.733+2314_733+2315d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18913541 | ||||||
| chr17:18913541 | C | CTTT | 32 | a0001c0001t0005g0359 a0001c0001t0005g0363 a0001c0001t0005g0366 others(29): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.733+2313_733+2315d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18913541 | ||||||
| chr17:18913541 | CT | C | 8 | a0001c0001t0001g0226 a0001c0001t0001g0246 a0001c0001t0001g0259 others(5): Show |
8 | HG00323.hp1 HG01346.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+2315delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18913541 | ||||||
| chr17:18913682 | G | C | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733+2431G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913682 | |||||||
| chr17:18913794 | C | T | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+2543C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913794 | |||||||
| chr17:18913903 | C | A | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+2652C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18913903 | |||||||
| chr17:18914067 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.733+2816G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914067 | |||||||
| chr17:18914110 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0318 |
2 | NA18985.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.733+2859G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914110 | |||||||
| chr17:18914143 | C | T | 19 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0359 others(16): Show |
19 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.733+2892C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914143 | |||||||
| chr17:18914173 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(81): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.733+2922C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914173 | |||||||
| chr17:18914215 | A | G | 1 | a0001c0002t0004g0140 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.733+2964A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914215 | |||||||
| chr17:18914249 | C | CT | 23 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0261 others(20): Show |
23 | HG00621.hp1 HG00673.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.733+3024dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0006g0191 a0001c0001t0006g0192 a0001c0001t0006g0193 others(3): Show |
6 | HG01109.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+3016_733+3024d others(11): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0006g0190 a0001c0003t0003g0007 a0001c0003t0003g0008 others(1): Show |
4 | HG02257.hp1 HG02818.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+3015_733+3024d others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0006g0195 a0001c0002t0004g0138 a0001c0002t0007g0358 others(4): Show |
7 | HG00741.hp2 HG01243.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+3014_733+3024d others(13): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | CTTTTTTT others(5): Show |
9 | a0001c0002t0004g0129 a0001c0002t0004g0133 a0001c0002t0004g0136 others(6): Show |
9 | HG00140.hp2 HG01167.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.733+3013_733+3024d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | CTTTTTTT others(6): Show |
10 | a0001c0002t0003g0028 a0001c0002t0004g0131 a0001c0002t0004g0135 others(7): Show |
10 | HG01169.hp2 HG01517.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+3012_733+3024d others(15): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | CTTTTTTT others(7): Show |
2 | a0001c0002t0004g0132 a0001c0002t0004g0146 |
2 | HG01106.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.733+3011_733+3024d others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | CTTTTTTT others(11): Show |
1 | a0001c0002t0004g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.733+3007_733+3024d others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914249 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.733+2998C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914249 | |||||||
| chr17:18914249 | CT | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(177): Show |
182 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.733+3024delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914249 | ||||||
| chr17:18914282 | G | C | 1 | a0001c0001t0001g0274 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.733+3031G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914282 | |||||||
| chr17:18914349 | C | G | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+3098C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914349 | |||||||
| chr17:18914370 | A | G | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.733+3119A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914370 | |||||||
| chr17:18914423 | A | AT | 77 | a0001c0001t0001g0283 a0001c0001t0001g0293 a0001c0001t0001g0297 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.733+3188dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914423 | ||||||
| chr17:18914449 | G | A | 3 | a0001c0001t0001g0343 a0001c0001t0001g0384 a0001c0001t0001g0390 |
3 | NA18983.hp2 NA19055.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.733+3198G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914449 | |||||||
| chr17:18914652 | T | A | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.733+3401T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914652 | |||||||
| chr17:18914729 | C | CT | 99 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0183 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.733+3491dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914729 | ||||||
| chr17:18914866 | A | G | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+3615A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914866 | |||||||
| chr17:18914914 | G | GGCATTCC others(22): Show |
1 | a0001c0001t0001g0333 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.733+3664_733+3692d others(31): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18914914 | ||||||
| chr17:18914915 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(79): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.733+3664G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914915 | |||||||
| chr17:18914976 | T | C | 1 | a0001c0002t0002g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.733+3725T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18914976 | |||||||
| chr17:18915022 | G | A | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+3771G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915022 | |||||||
| chr17:18915022 | G | C | 1 | a0001c0001t0005g0375 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.733+3771G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915022 | |||||||
| chr17:18915025 | C | CT | 106 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.733+3791dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18915025 | ||||||
| chr17:18915025 | C | CTT | 28 | a0001c0001t0001g0243 a0001c0001t0001g0271 a0001c0001t0002g0123 others(25): Show |
28 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.733+3790_733+3791d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18915025 | ||||||
| chr17:18915152 | A | G | 300 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(297): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.733+3901A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915152 | |||||||
| chr17:18915215 | G | A | 1 | a0001c0002t0003g0018 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.733+3964G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915215 | |||||||
| chr17:18915244 | T | C | 19 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0359 others(16): Show |
19 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.733+3993T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915244 | |||||||
| chr17:18915263 | C | T | 1 | a0001c0002t0004g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.733+4012C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915263 | |||||||
| chr17:18915318 | G | A | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+4067G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915318 | |||||||
| chr17:18915339 | T | C | 3 | a0001c0001t0005g0360 a0001c0001t0005g0365 a0001c0001t0005g0386 |
3 | HG00408.hp2 NA19060.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.733+4088T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915339 | |||||||
| chr17:18915485 | C | CA | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+4234_733+4235i others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915485 | |||||||
| chr17:18915646 | C | T | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+4395C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915646 | |||||||
| chr17:18915734 | G | A | 6 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(3): Show |
6 | HG02055.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+4483G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915734 | |||||||
| chr17:18915779 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.733+4528C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18915779 | |||||||
| chr17:18915822 | AT | A | 34 | a0001c0001t0001g0183 a0001c0001t0001g0198 a0001c0001t0001g0276 others(31): Show |
34 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.733+4586delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18915822 | ||||||
| chr17:18916069 | C | T | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+4818C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916069 | |||||||
| chr17:18916128 | A | T | 3 | a0001c0001t0006g0191 a0001c0001t0006g0192 a0001c0001t0006g0193 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.733+4877A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916128 | |||||||
| chr17:18916130 | A | G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0302 |
2 | HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.733+4879A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916130 | |||||||
| chr17:18916205 | A | G | 1 | a0001c0002t0002g0153 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.733+4954A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916205 | |||||||
| chr17:18916279 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.733+5028C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916279 | |||||||
| chr17:18916376 | A | AT | 34 | a0001c0001t0001g0199 a0001c0001t0001g0215 a0001c0001t0001g0269 others(31): Show |
34 | HG00140.hp2 HG01099.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.733+5141dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18916376 | ||||||
| chr17:18916457 | C | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG00099.hp2 HG00733.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+5206C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916457 | |||||||
| chr17:18916484 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.733+5233C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916484 | |||||||
| chr17:18916599 | C | T | 1 | a0001c0001t0001g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.733+5348C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916599 | |||||||
| chr17:18916672 | G | A | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.733+5421G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916672 | |||||||
| chr17:18916933 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.733+5682A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18916933 | |||||||
| chr17:18917144 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(105): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.733+5893C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917144 | |||||||
| chr17:18917162 | C | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0277 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.733+5911C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917162 | |||||||
| chr17:18917189 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.733+5938G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917189 | |||||||
| chr17:18917397 | CT | C | 35 | a0001c0001t0001g0226 a0001c0001t0001g0325 a0001c0001t0001g0341 others(32): Show |
35 | HG00140.hp2 HG00323.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.733+6161delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917397 | ||||||
| chr17:18917546 | G | GTAT | 4 | a0001c0001t0001g0281 a0001c0001t0001g0304 a0001c0001t0005g0366 others(1): Show |
4 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-6330_734-6328d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917546 | ||||||
| chr17:18917546 | GTAT | G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0271 a0001c0002t0003g0024 |
3 | HG02293.hp1 HG04115.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.734-6330_734-6328d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917546 | ||||||
| chr17:18917546 | GTATTAT | G | 3 | a0001c0001t0001g0226 a0001c0002t0002g0084 a0001c0002t0002g0119 |
3 | HG00323.hp1 HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.733+6330_734-6328d others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917546 | ||||||
| chr17:18917569 | ATTATTAT others(16): Show |
A | 8 | a0001c0003t0003g0005 a0001c0003t0003g0006 a0001c0003t0003g0007 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+6321_734-6320d others(25): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917569 | ||||||
| chr17:18917572 | ATTATTAT others(9): Show |
A | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733+6324_734-6324d others(18): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917572 | ||||||
| chr17:18917572 | ATTATTAT others(10): Show |
A | 4 | a0001c0001t0006g0191 a0001c0001t0006g0192 a0001c0001t0006g0193 others(1): Show |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+6324_734-6323d others(19): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917572 | ||||||
| chr17:18917572 | ATTATTAT others(11): Show |
A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.733+6324_734-6322d others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917572 | ||||||
| chr17:18917575 | ATTATTAT others(6): Show |
A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0312 a0001c0001t0001g0332 |
3 | HG00738.hp2 NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.733+6327_734-6324d others(15): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917575 | ||||||
| chr17:18917575 | ATTATTAT others(8): Show |
A | 2 | a0001c0002t0002g0164 a0001c0002t0002g0167 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.733+6327_734-6322d others(17): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917575 | ||||||
| chr17:18917575 | ATTATTAT others(10): Show |
A | 2 | a0001c0001t0006g0190 a0001c0001t0006g0195 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.733+6327_734-6320d others(19): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917575 | ||||||
| chr17:18917577 | TATTATTA | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02886.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+6327_734-6330d others(9): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917577 | |||||||
| chr17:18917578 | ATTATTAT others(5): Show |
A | 2 | a0001c0002t0002g0160 a0001c0002t0002g0161 |
2 | HG02132.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.733+6330_734-6322d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917578 | ||||||
| chr17:18917578 | ATTATTAT others(7): Show |
A | 1 | a0001c0002t0002g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.733+6330_734-6320d others(16): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917578 | ||||||
| chr17:18917578 | ATTATTAT others(8): Show |
A | 10 | a0001c0001t0002g0171 a0001c0002t0002g0152 a0001c0002t0002g0157 others(7): Show |
10 | HG02145.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+6330_734-6319d others(17): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917578 | ||||||
| chr17:18917580 | TATTA | T | 3 | a0001c0001t0001g0236 a0001c0002t0003g0023 a0001c0002t0003g0030 |
3 | HG01123.hp1 HG01934.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.733+6330_734-6330d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917580 | |||||||
| chr17:18917581 | A | T | 1 | a0001c0002t0002g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.733+6330A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917581 | |||||||
| chr17:18917581 | ATTAT | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0214 a0001c0001t0001g0244 others(4): Show |
7 | HG00733.hp1 HG01123.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-6330_734-6327d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917581 | ||||||
| chr17:18917581 | ATTATTTT others(8): Show |
A | 2 | a0001c0002t0002g0126 a0001c0002t0002g0176 |
2 | HG02738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.734-6330_734-6316d others(17): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917581 | ||||||
| chr17:18917581 | ATTATTTT others(11): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.734-6330_734-6313d others(20): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917581 | ||||||
| chr17:18917582 | TTA | T | 14 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(11): Show |
14 | HG01346.hp1 HG01884.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-6330_734-6329d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917582 | ||||||
| chr17:18917583 | TA | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0321 a0001c0001t0001g0336 others(2): Show |
5 | HG02129.hp1 HG02523.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-6330delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917583 | |||||||
| chr17:18917584 | A | T | 10 | a0001c0001t0001g0296 a0001c0001t0001g0324 a0001c0001t0001g0340 others(7): Show |
10 | HG01109.hp2 HG01175.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-6330A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917584 | |||||||
| chr17:18917584 | AT | A | 58 | a0001c0001t0001g0187 a0001c0001t0001g0206 a0001c0001t0001g0208 others(55): Show |
58 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.734-6295delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917584 | ||||||
| chr17:18917584 | ATT | A | 71 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0216 others(68): Show |
72 | HG00408.hp1 HG00558.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.734-6296_734-6295d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917584 | ||||||
| chr17:18917584 | ATTT | A | 10 | a0001c0001t0001g0331 a0001c0002t0002g0043 a0001c0002t0002g0049 others(7): Show |
10 | HG00323.hp2 HG00558.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-6297_734-6295d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917584 | ||||||
| chr17:18917584 | ATTTT | A | 19 | a0001c0001t0001g0181 a0001c0001t0001g0202 a0001c0001t0001g0215 others(16): Show |
19 | HG00738.hp1 HG01106.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.734-6298_734-6295d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917584 | ||||||
| chr17:18917584 | ATTTTT | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0220 a0001c0001t0001g0227 others(32): Show |
35 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.734-6299_734-6295d others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917584 | ||||||
| chr17:18917584 | ATTTTTT | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0196 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.734-6300_734-6295d others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917584 | ||||||
| chr17:18917584 | ATTTTTTT others(8): Show |
A | 1 | a0001c0002t0002g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.734-6309_734-6295d others(17): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917584 | ||||||
| chr17:18917585 | T | TTA | 16 | a0001c0001t0001g0207 a0001c0001t0001g0290 a0001c0001t0001g0319 others(13): Show |
16 | HG00099.hp1 HG00408.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.734-6328_734-6327i others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18917585 | ||||||
| chr17:18917586 | T | TA | 14 | a0001c0001t0005g0189 a0001c0001t0005g0361 a0001c0001t0005g0369 others(11): Show |
14 | HG00423.hp1 HG01070.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-6328_734-6327i others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917586 | |||||||
| chr17:18917586 | T | TATTA | 5 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0355 others(2): Show |
5 | HG02027.hp2 HG02080.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-6328_734-6327i others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917586 | |||||||
| chr17:18917586 | T | TATTATTA | 3 | a0001c0001t0001g0329 a0001c0002t0002g0089 a0001c0002t0002g0093 |
3 | HG01070.hp2 HG01071.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.734-6328_734-6327i others(9): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917586 | |||||||
| chr17:18917587 | T | A | 28 | a0001c0001t0001g0198 a0001c0001t0001g0281 a0001c0001t0001g0304 others(25): Show |
28 | HG00140.hp2 HG01074.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.734-6327T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917587 | |||||||
| chr17:18917588 | T | A | 53 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(50): Show |
53 | HG00621.hp2 HG00673.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.734-6326T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917588 | |||||||
| chr17:18917589 | T | A | 74 | a0001c0001t0001g0216 a0001c0001t0001g0223 a0001c0001t0001g0225 others(71): Show |
75 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.734-6325T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917589 | |||||||
| chr17:18917590 | T | A | 18 | a0001c0001t0001g0306 a0001c0001t0001g0325 a0001c0001t0001g0331 others(15): Show |
18 | HG00323.hp2 HG00558.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.734-6324T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917590 | |||||||
| chr17:18917591 | T | A | 22 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0212 others(19): Show |
22 | HG01167.hp1 HG01256.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.734-6323T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917591 | |||||||
| chr17:18917592 | T | A | 39 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0001g0233 others(36): Show |
39 | HG00140.hp1 HG00558.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.734-6322T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917592 | |||||||
| chr17:18917593 | T | A | 10 | a0001c0001t0001g0196 a0001c0001t0001g0388 a0001c0002t0002g0043 others(7): Show |
10 | HG00323.hp2 HG00733.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-6321T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917593 | |||||||
| chr17:18917594 | T | A | 5 | a0001c0001t0001g0212 a0001c0001t0001g0309 a0001c0001t0001g0353 others(2): Show |
5 | HG01884.hp1 HG01934.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-6320T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917594 | |||||||
| chr17:18917595 | T | A | 4 | a0001c0002t0002g0033 a0001c0002t0002g0039 a0001c0002t0002g0117 others(1): Show |
4 | HG00735.hp2 HG02040.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-6319T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917595 | |||||||
| chr17:18917597 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.734-6317T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917597 | |||||||
| chr17:18917598 | T | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-6316T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917598 | |||||||
| chr17:18917601 | T | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-6313T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917601 | |||||||
| chr17:18917604 | T | A | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.734-6310T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917604 | |||||||
| chr17:18917605 | T | A | 31 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(28): Show |
31 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.734-6309T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917605 | |||||||
| chr17:18917606 | T | A | 1 | a0001c0001t0001g0310 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.734-6308T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917606 | |||||||
| chr17:18917615 | T | A | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-6299T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917615 | |||||||
| chr17:18917672 | A | T | 122 | a0001c0001t0001g0235 a0001c0001t0002g0171 a0001c0002t0002g0001 others(119): Show |
123 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.734-6242A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917672 | |||||||
| chr17:18917866 | A | C | 3 | a0001c0002t0002g0154 a0001c0002t0002g0155 a0001c0002t0002g0156 |
3 | HG01433.hp2 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.734-6048A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18917866 | |||||||
| chr17:18918075 | A | G | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.734-5839A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918075 | |||||||
| chr17:18918122 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.734-5792G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918122 | |||||||
| chr17:18918316 | G | C | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | NA18959.hp2 NA18964.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-5598G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918316 | |||||||
| chr17:18918512 | C | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.734-5402C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918512 | |||||||
| chr17:18918562 | C | G | 1 | a0001c0001t0001g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-5352C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918562 | |||||||
| chr17:18918579 | A | G | 2 | a0001c0001t0001g0350 a0001c0001t0001g0351 |
2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.734-5335A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918579 | |||||||
| chr17:18918666 | C | T | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.734-5248C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918666 | |||||||
| chr17:18918745 | T | C | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.734-5169T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918745 | |||||||
| chr17:18918746 | G | A | 2 | a0001c0002t0004g0143 a0001c0002t0004g0150 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.734-5168G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918746 | |||||||
| chr17:18918854 | T | G | 23 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0359 others(20): Show |
23 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.734-5060T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18918854 | |||||||
| chr17:18919100 | G | A | 7 | a0001c0002t0002g0086 a0001c0002t0002g0089 a0001c0002t0002g0093 others(4): Show |
7 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-4814G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919100 | |||||||
| chr17:18919157 | G | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.734-4757G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919157 | |||||||
| chr17:18919191 | C | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.734-4723C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919191 | |||||||
| chr17:18919194 | C | T | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.734-4720C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919194 | |||||||
| chr17:18919274 | C | T | 10 | a0001c0001t0001g0198 a0001c0001t0001g0201 a0001c0001t0001g0253 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-4640C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919274 | |||||||
| chr17:18919313 | A | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(287): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.734-4601A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919313 | |||||||
| chr17:18919313 | A | T | 1 | a0001c0002t0004g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.734-4601A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919313 | |||||||
| chr17:18919643 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.734-4271G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919643 | |||||||
| chr17:18919798 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.734-4116A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919798 | |||||||
| chr17:18919849 | T | C | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.734-4065T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919849 | |||||||
| chr17:18919881 | T | G | 1 | a0001c0002t0004g0144 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.734-4033T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18919881 | |||||||
| chr17:18920049 | G | A | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.734-3865G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18920049 | |||||||
| chr17:18920265 | T | C | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.734-3649T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18920265 | |||||||
| chr17:18920294 | G | A | 17 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.734-3620G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18920294 | |||||||
| chr17:18920391 | C | T | 1 | a0001c0001t0001g0389 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-3523C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18920391 | |||||||
| chr17:18920392 | G | A | 68 | a0001c0001t0002g0171 a0001c0001t0006g0190 a0001c0001t0006g0191 others(65): Show |
68 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.734-3522G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18920392 | |||||||
| chr17:18920931 | CCTT | C | 15 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(12): Show |
15 | HG00741.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-2980_734-2978d others(5): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18920931 | ||||||
| chr17:18920973 | A | G | 8 | a0001c0001t0002g0171 a0001c0002t0002g0167 a0001c0002t0002g0169 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-2941A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18920973 | |||||||
| chr17:18921236 | AATAT | A | 15 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(12): Show |
15 | HG00741.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-2675_734-2672d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18921236 | ||||||
| chr17:18921239 | A | G | 44 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0003g0015 others(41): Show |
44 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.734-2675A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18921239 | |||||||
| chr17:18921249 | A | AAAAAGTG others(10): Show |
15 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(12): Show |
15 | HG00741.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-2662_734-2661i others(19): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18921249 | ||||||
| chr17:18921648 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.734-2266G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18921648 | |||||||
| chr17:18921677 | C | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0322 |
2 | NA18992.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.734-2237C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18921677 | |||||||
| chr17:18921732 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.734-2182C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18921732 | |||||||
| chr17:18921890 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-2024A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18921890 | |||||||
| chr17:18922668 | A | AT | 135 | a0001c0001t0001g0186 a0001c0001t0001g0199 a0001c0001t0001g0209 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.734-1223dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18922668 | ||||||
| chr17:18922668 | A | ATT | 34 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0211 others(31): Show |
34 | HG00621.hp2 HG01081.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.734-1224_734-1223d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18922668 | ||||||
| chr17:18922668 | A | T | 2 | a0001c0001t0001g0333 a0001c0002t0002g0103 |
2 | NA18974.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.734-1246A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18922668 | |||||||
| chr17:18922668 | AT | A | 13 | a0001c0001t0001g0382 a0001c0001t0005g0377 a0001c0002t0004g0127 others(10): Show |
13 | HG01070.hp1 HG01169.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-1223delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18922668 | ||||||
| chr17:18922668 | ATT | A | 10 | a0001c0002t0004g0131 a0001c0002t0004g0134 a0001c0002t0004g0138 others(7): Show |
10 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-1224_734-1223d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18922668 | ||||||
| chr17:18922668 | ATTTTT | A | 29 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(26): Show |
29 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.734-1227_734-1223d others(7): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18922668 | ||||||
| chr17:18922744 | G | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0349 |
2 | NA18939.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.734-1170G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18922744 | |||||||
| chr17:18922913 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.734-1001A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18922913 | |||||||
| chr17:18922940 | A | G | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.734-974A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18922940 | |||||||
| chr17:18922976 | G | A | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.734-938G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18922976 | |||||||
| chr17:18923024 | T | C | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-890T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18923024 | |||||||
| chr17:18923053 | T | G | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.734-861T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18923053 | |||||||
| chr17:18923077 | CTATTTAT others(7): Show |
C | 32 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(29): Show |
32 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.734-821_734-808del others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18923077 | ||||||
| chr17:18923160 | G | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.734-754G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18923160 | |||||||
| chr17:18923256 | A | AT | 63 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0261 others(60): Show |
63 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.734-635dupT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18923256 | ||||||
| chr17:18923256 | A | ATT | 8 | a0001c0001t0001g0250 a0001c0002t0003g0019 a0001c0002t0003g0025 others(5): Show |
8 | HG00544.hp1 HG01433.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-636_734-635dup others(2): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18923256 | ||||||
| chr17:18923256 | AT | A | 8 | a0001c0001t0001g0217 a0001c0001t0001g0229 a0001c0001t0001g0266 others(5): Show |
8 | HG01167.hp2 HG01975.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-635delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18923256 | ||||||
| chr17:18923307 | C | T | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.734-607C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18923307 | |||||||
| chr17:18923405 | G | A | 2 | a0001c0003t0003g0005 a0001c0003t0003g0012 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.734-509G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | chr17 | 18923405 | |||||||
| chr17:18923507 | ATAT | A | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.734-401_734-399del others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 18923507 | ||||||
| chr17:18924035 | GTTGA | G | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+70_804+73delGA others(2): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18924035 | ||||||
| chr17:18924078 | C | T | 24 | a0001c0001t0002g0112 a0001c0001t0005g0189 a0001c0001t0005g0359 others(21): Show |
24 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.804+94C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924078 | |||||||
| chr17:18924108 | C | T | 1 | a0001c0002t0002g0035 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.804+124C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924108 | |||||||
| chr17:18924147 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.804+163C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924147 | |||||||
| chr17:18924291 | C | T | 1 | a0001c0002t0003g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.804+307C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924291 | |||||||
| chr17:18924360 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0198 a0001c0001t0001g0201 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.804+376G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924360 | |||||||
| chr17:18924478 | C | G | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.804+494C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924478 | |||||||
| chr17:18924480 | C | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.804+496C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924480 | |||||||
| chr17:18924495 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.804+511G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924495 | |||||||
| chr17:18924597 | T | C | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.804+613T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924597 | |||||||
| chr17:18924652 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.804+668C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924652 | |||||||
| chr17:18924674 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.804+690C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18924674 | |||||||
| chr17:18924768 | C | CA | 17 | a0001c0001t0001g0180 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG02027.hp2 HG02071.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+803dupA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18924768 | ||||||
| chr17:18924768 | CA | C | 36 | a0001c0001t0001g0261 a0001c0001t0006g0190 a0001c0001t0006g0191 others(33): Show |
36 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.804+803delA | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18924768 | ||||||
| chr17:18924768 | CAA | C | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.804+802_804+803del others(2): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18924768 | ||||||
| chr17:18925093 | C | T | 5 | a0001c0002t0002g0063 a0001c0002t0002g0064 a0001c0002t0002g0068 others(2): Show |
5 | HG01167.hp2 HG01361.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1109C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925093 | |||||||
| chr17:18925124 | G | A | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+1140G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925124 | |||||||
| chr17:18925347 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.804+1363C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925347 | |||||||
| chr17:18925390 | G | A | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+1406G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925390 | |||||||
| chr17:18925612 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.804+1628G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925612 | |||||||
| chr17:18925902 | G | A | 4 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | NA18983.hp1 NA18988.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+1918G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925902 | |||||||
| chr17:18925932 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.804+1948T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925932 | |||||||
| chr17:18925950 | A | G | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+1966A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925950 | |||||||
| chr17:18925967 | T | C | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.804+1983T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18925967 | |||||||
| chr17:18926046 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.804+2062C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926046 | |||||||
| chr17:18926073 | A | G | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+2089A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926073 | |||||||
| chr17:18926236 | A | ATTAT | 133 | a0001c0001t0001g0002 a0001c0001t0001g0181 a0001c0001t0001g0182 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.804+2283_804+2286d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926236 | ||||||
| chr17:18926236 | A | ATTATTTA others(1): Show |
5 | a0001c0001t0001g0248 a0001c0001t0001g0388 a0001c0001t0006g0190 others(2): Show |
5 | HG02818.hp1 HG03098.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2279_804+2286d others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926236 | ||||||
| chr17:18926236 | A | ATTATTTA others(5): Show |
5 | a0001c0001t0006g0191 a0001c0001t0006g0192 a0001c0001t0006g0193 others(2): Show |
5 | HG02055.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2275_804+2286d others(14): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926236 | ||||||
| chr17:18926236 | ATTAT | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0278 a0001c0001t0001g0382 |
3 | HG00323.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.804+2283_804+2286d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926236 | ||||||
| chr17:18926259 | A | C | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.804+2275A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926259 | |||||||
| chr17:18926261 | T | A | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.804+2277T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926261 | |||||||
| chr17:18926262 | TATTTATT others(4): Show |
T | 26 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(23): Show |
26 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.804+2279_804+2289d others(13): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926262 | |||||||
| chr17:18926720 | G | A | 293 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.805-2091G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926720 | |||||||
| chr17:18926763 | AT | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.805-2047delT | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926763 | |||||||
| chr17:18926777 | A | AGT | 86 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0001g0200 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.805-2009_805-2008d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926777 | ||||||
| chr17:18926777 | A | AGTGT | 16 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(13): Show |
16 | HG00544.hp1 HG01943.hp2 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.805-2011_805-2008d others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926777 | ||||||
| chr17:18926777 | A | AGTGTGT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0221 a0001c0001t0001g0356 others(7): Show |
11 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.805-2013_805-2008d others(8): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926777 | ||||||
| chr17:18926777 | AGT | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0389 a0001c0002t0002g0077 |
3 | HG02559.hp1 NA18939.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.805-2009_805-2008d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926777 | ||||||
| chr17:18926777 | AGTGTGTG others(1): Show |
A | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.805-2015_805-2008d others(10): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18926777 | ||||||
| chr17:18926810 | T | G | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.805-2001T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926810 | |||||||
| chr17:18926811 | T | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0274 |
2 | HG00140.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.805-2000T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926811 | |||||||
| chr17:18926878 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.805-1933C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926878 | |||||||
| chr17:18926943 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.805-1868C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926943 | |||||||
| chr17:18926974 | G | A | 67 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.805-1837G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18926974 | |||||||
| chr17:18927355 | C | T | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.805-1456C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927355 | |||||||
| chr17:18927472 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.805-1339A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927472 | |||||||
| chr17:18927497 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1314T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927497 | |||||||
| chr17:18927498 | G | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1313G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927498 | |||||||
| chr17:18927500 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1311T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927500 | |||||||
| chr17:18927501 | G | GCCAATAA others(3): Show |
1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1310_805-1309i others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927501 | |||||||
| chr17:18927504 | C | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1307C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927504 | |||||||
| chr17:18927506 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1305G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927506 | |||||||
| chr17:18927509 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1302T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927509 | |||||||
| chr17:18927510 | C | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1301C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927510 | |||||||
| chr17:18927511 | C | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1300C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927511 | |||||||
| chr17:18927520 | A | T | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1291A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927520 | |||||||
| chr17:18927521 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1290G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927521 | |||||||
| chr17:18927523 | G | T | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1288G>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927523 | |||||||
| chr17:18927524 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1287G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927524 | |||||||
| chr17:18927528 | C | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1283C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927528 | |||||||
| chr17:18927530 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1281G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927530 | |||||||
| chr17:18927532 | G | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1279G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927532 | |||||||
| chr17:18927533 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1278T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927533 | |||||||
| chr17:18927534 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1277T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927534 | |||||||
| chr17:18927535 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1276T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927535 | |||||||
| chr17:18927536 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1275A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927536 | |||||||
| chr17:18927539 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.805-1272T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927539 | |||||||
| chr17:18927540 | G | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1271G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927540 | |||||||
| chr17:18927541 | T | G | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1270T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927541 | |||||||
| chr17:18927561 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1250T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927561 | |||||||
| chr17:18927576 | A | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1235A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927576 | |||||||
| chr17:18927580 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1231T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927580 | |||||||
| chr17:18927596 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1215T>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927596 | |||||||
| chr17:18927599 | A | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1212A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927599 | |||||||
| chr17:18927600 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1211C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927600 | |||||||
| chr17:18927619 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1192G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927619 | |||||||
| chr17:18927621 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1190G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927621 | |||||||
| chr17:18927627 | AGAGTTTT others(3): Show |
A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1183_805-1174d others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927627 | |||||||
| chr17:18927646 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1165G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927646 | |||||||
| chr17:18927653 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1158G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927653 | |||||||
| chr17:18927654 | C | G | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1157C>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927654 | |||||||
| chr17:18927656 | C | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1155C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927656 | |||||||
| chr17:18927657 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1154T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927657 | |||||||
| chr17:18927658 | T | G | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1153T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927658 | |||||||
| chr17:18927664 | T | G | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1147T>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927664 | |||||||
| chr17:18927670 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.805-1141T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927670 | |||||||
| chr17:18927693 | G | A | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.805-1118G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927693 | |||||||
| chr17:18927735 | G | A | 2 | a0001c0001t0005g0362 a0001c0001t0005g0369 |
2 | HG00423.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.805-1076G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927735 | |||||||
| chr17:18927770 | C | CGT | 3 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0080 |
3 | HG02004.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.805-1028_805-1027d others(4): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 18927770 | ||||||
| chr17:18927772 | T | C | 2 | a0001c0001t0005g0365 a0001c0001t0005g0386 |
2 | NA19060.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.805-1039T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927772 | |||||||
| chr17:18927939 | T | C | 22 | a0001c0002t0004g0131 a0001c0002t0004g0132 a0001c0002t0004g0133 others(19): Show |
22 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.805-872T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18927939 | |||||||
| chr17:18928037 | G | C | 1 | a0001c0002t0002g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.805-774G>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928037 | |||||||
| chr17:18928119 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.805-692A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928119 | |||||||
| chr17:18928195 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.805-616C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928195 | |||||||
| chr17:18928201 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.805-610G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928201 | |||||||
| chr17:18928641 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.805-170C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928641 | |||||||
| chr17:18928653 | A | T | 1 | a0001c0002t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.805-158A>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928653 | |||||||
| chr17:18928654 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.805-157C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928654 | |||||||
| chr17:18928679 | C | T | 1 | a0001c0002t0002g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.805-132C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928679 | |||||||
| chr17:18928716 | C | T | 1 | a0001c0002t0009g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.805-95C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 10/11 | chr17 | 18928716 | |||||||
| chr17:18928983 | T | C | 1 | a0001c0002t0002g0039 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.951+26T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18928983 | |||||||
| chr17:18929078 | T | C | 6 | a0001c0002t0002g0115 a0001c0002t0002g0116 a0001c0002t0002g0117 others(3): Show |
6 | NA18965.hp2 NA18967.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.951+121T>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18929078 | |||||||
| chr17:18929285 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.951+328G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18929285 | |||||||
| chr17:18929358 | A | AAAT | 126 | a0001c0001t0001g0198 a0001c0001t0001g0212 a0001c0001t0001g0235 others(123): Show |
127 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.951+432_951+434dup others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 18929358 | ||||||
| chr17:18929358 | A | AAATAAT | 34 | a0001c0001t0001g0293 a0001c0001t0001g0308 a0001c0001t0005g0366 others(31): Show |
34 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.951+429_951+434dup others(6): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 18929358 | ||||||
| chr17:18929358 | A | AAATAATA others(2): Show |
37 | a0001c0002t0002g0035 a0001c0002t0002g0047 a0001c0002t0002g0048 others(34): Show |
37 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.951+426_951+434dup others(9): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 18929358 | ||||||
| chr17:18929358 | A | AAATAATA others(5): Show |
13 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(10): Show |
13 | HG01884.hp2 HG02257.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.951+423_951+434dup others(12): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 18929358 | ||||||
| chr17:18929358 | A | AAATAATA others(8): Show |
3 | a0001c0001t0006g0194 a0001c0001t0006g0195 a0001c0002t0004g0128 |
3 | HG01109.hp2 HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.951+420_951+434dup others(15): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 18929358 | ||||||
| chr17:18929358 | A | AAATAATA others(11): Show |
1 | a0001c0002t0007g0358 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.951+417_951+434dup others(18): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 18929358 | ||||||
| chr17:18929358 | AAAT | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0203 others(2): Show |
5 | HG03471.hp2 HG03579.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+432_951+434del others(3): Show |
PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 18929358 | ||||||
| chr17:18929483 | C | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0298 |
2 | NA18973.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.951+526C>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18929483 | |||||||
| chr17:18929525 | A | C | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0305 others(1): Show |
4 | HG00673.hp2 HG02135.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.951+568A>C | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18929525 | |||||||
| chr17:18929749 | C | T | 27 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 others(24): Show |
27 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.952-791C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18929749 | |||||||
| chr17:18930168 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.952-372C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18930168 | |||||||
| chr17:18930169 | G | A | 1 | a0001c0002t0003g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.952-371G>A | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18930169 | |||||||
| chr17:18930233 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.952-307C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18930233 | |||||||
| chr17:18930299 | A | G | 59 | a0001c0001t0006g0190 a0001c0001t0006g0191 a0001c0001t0006g0192 others(56): Show |
59 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.952-241A>G | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18930299 | |||||||
| chr17:18930497 | C | T | 90 | a0001c0002t0002g0001 a0001c0002t0002g0032 a0001c0002t0002g0033 others(87): Show |
91 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.952-43C>T | PRPSAP2 | ENSG00000141127.15 | transcript | ENST00000268835.7 | protein_coding | 11/11 | chr17 | 18930497 |