Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5546 |
| ensemblid | ENSG00000143294.15 |
| hgncid | 9343 |
| symbol | PRCC |
| name | proline rich mitotic checkpoint control factor |
| refseq_nuc | NM_005973.5 |
| refseq_prot | NP_005964.3 |
| ensembl_nuc | ENST00000271526.9 |
| ensembl_prot | ENSP00000271526.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 156767535 |
| end | 156800815 |
| strand | + |
| ver | v1.2 |
| region | chr1:156767535-156800815 |
| region5000 | chr1:156762535-156805815 |
| regionname0 | PRCC_chr1_156767535_156800815 |
| regionname5000 | PRCC_chr1_156762535_156805815 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 491 | 294 | 92 | 55 | 101 | 7 | 37 | 73 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| a0002 | 0/0 | 491 | 48 | 4 | 20 | 16 | 3 | 5 | 10 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| a0003 | 0/0 | 491 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| a0004 | 0/0 | 491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| a0005 | 0/0 | 491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| a0006 | 0/0 | 491 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| a0007 | 0/0 | 491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| a0008 | 0/0 | 491 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | MSLVA others(486): Show |
chr1 | 156762535 | 156805815 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1473 | 292 | 91 | 54 | 101 | 7 | 37 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0001c0004 | 0/0 | 1473 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0001c0007 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0002c0002 | 0/0 | 1473 | 48 | 4 | 20 | 16 | 3 | 5 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0003c0003 | 0/0 | 1473 | 3 | 0 | 2 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0004c0010 | 0/0 | 1473 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0005c0008 | 0/0 | 1473 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0006c0009 | 0/0 | 1473 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0007c0006 | 0/0 | 1473 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 | ||
| a0008c0005 | 0/0 | 1473 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | ATGTC others(1468): Show |
chr1 | 156762535 | 156805815 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2068 | 286 | 88 | 53 | 101 | 7 | 35 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0001c0001t0003 | 0/0 | 2068 | 2 | 2 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0001c0001t0004 | 0/0 | 2068 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0001c0001t0005 | 0/0 | 2068 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0001c0001t0006 | 0/0 | 2068 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0001c0001t0008 | 0/0 | 2068 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0001c0004t0001 | 0/0 | 2068 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0001c0007t0001 | 0/0 | 2068 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0002c0002t0001 | 0/0 | 2068 | 43 | 4 | 17 | 15 | 3 | 4 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0002c0002t0002 | 0/0 | 2067 | 4 | 0 | 3 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2062): Show |
chr1 | 156762535 | 156805815 |
| a0002c0002t0007 | 0/0 | 2068 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0003c0003t0001 | 0/0 | 2068 | 3 | 0 | 2 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0004c0010t0001 | 0/0 | 2068 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0005c0008t0001 | 0/0 | 2068 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0006c0009t0001 | 0/0 | 2068 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0007c0006t0001 | 0/0 | 2068 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| a0008c0005t0001 | 0/0 | 2068 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | GGCCA others(2063): Show |
chr1 | 156762535 | 156805815 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0001c0007t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0002c0002t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0004c0010t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0005c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0006c0009t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0007c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| a0008c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | GBR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0130 | EUR | GBR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0046 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01243 | hp1 | a0004 | c0010 | t0001 | g0244 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0064 | AMR | PUR | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0117 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0120 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | CLM | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0159 | EUR | IBS | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0163 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0237 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0148 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02027 | hp1 | a0005 | c0008 | t0001 | g0219 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0045 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0067 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03654 | hp1 | a0006 | c0009 | t0001 | g0050 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0134 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0063 | SAS | PJL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0256 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18747 | hp1 | a0007 | c0006 | t0001 | g0002 | EAS | CHB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18961 | hp2 | a0002 | c0002 | t0007 | g0115 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19079 | hp1 | a0008 | c0005 | t0001 | g0061 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ASW | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ASW | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0140 | EUR | TSI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | GIH | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | GIH | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | USA | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | USA | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | USA | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0166 | REF | REF | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0106 | REF | REF | PRCC_chr1_156762535_156805815 | PRCC | chr1 | 156762535 | 156805815 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156767965 | C | T | 1 | a0004 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.194C>T | p.Pro65Leu | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/7 | 431/2068 | 194/1476 | 65/491 | chr1 | 156767965 | |||
| chr1:156767967 | C | G | 1 | a0006 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.196C>G | p.Leu66Val | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/7 | 433/2068 | 196/1476 | 66/491 | chr1 | 156767967 | |||
| chr1:156768043 | C | G | 1 | a0005 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.272C>G | p.Pro91Arg | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/7 | 509/2068 | 272/1476 | 91/491 | chr1 | 156768043 | |||
| chr1:156768177 | C | T | 1 | a0002 | 48 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
missense_variant | MODERATE | c.406C>T | p.Pro136Ser | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/7 | 643/2068 | 406/1476 | 136/491 | chr1 | 156768177 | |||
| chr1:156786693 | C | G | 1 | a0007 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.602C>G | p.Pro201Arg | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/7 | 839/2068 | 602/1476 | 201/491 | chr1 | 156786693 | |||
| chr1:156786776 | C | T | 1 | a0008 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.685C>T | p.Leu229Phe | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/7 | 922/2068 | 685/1476 | 229/491 | chr1 | 156786776 | |||
| chr1:156791748 | C | A | 1 | a0003 | 3 | HG00639.hp1 HG01243.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.1135C>A | p.Pro379Thr | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/7 | 1372/2068 | 1135/1476 | 379/491 | chr1 | 156791748 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156768140 | C | T | 1 | a0001c0007 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.369C>T | p.Pro123Pro | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/7 | 606/2068 | 369/1476 | 123/491 | chr1 | 156768140 | |||
| chr1:156786814 | G | A | 1 | a0001c0004 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.723G>A | p.Ser241Ser | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/7 | 960/2068 | 723/1476 | 241/491 | chr1 | 156786814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156767731 | C | T | 1 | a0001c0001t0008 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/7 | 41 | chr1 | 156767731 | ||||||
| chr1:156800515 | C | G | 1 | a0002c0002t0007 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 7/7 | 55 | chr1 | 156800515 | ||||||
| chr1:156800530 | G | A | 1 | a0001c0001t0004 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 7/7 | 70 | chr1 | 156800530 | ||||||
| chr1:156800678 | C | T | 1 | a0001c0001t0006 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*218C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 7/7 | 218 | chr1 | 156800678 | ||||||
| chr1:156800715 | G | A | 1 | a0001c0001t0005 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 7/7 | 255 | chr1 | 156800715 | ||||||
| chr1:156800790 | TG | T | 1 | a0002c0002t0002 | 4 | HG01256.hp1 HG01258.hp1 HG01928.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*331delG | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 7/7 | 331 | chr1 | 156800790 | ||||||
| chr1:156800812 | C | A | 1 | a0001c0001t0003 | 2 | HG02615.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*352C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 7/7 | 352 | chr1 | 156800812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156768479 | C | T | 27 | a0001c0001t0001g0015 a0001c0001t0001g0302 a0001c0001t0001g0303 others(24): Show |
28 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+240C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768479 | |||||||
| chr1:156768636 | T | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.468+397T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768636 | |||||||
| chr1:156768672 | A | G | 27 | a0001c0001t0001g0015 a0001c0001t0001g0302 a0001c0001t0001g0303 others(24): Show |
28 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+433A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768672 | |||||||
| chr1:156768673 | G | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02258.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.468+434G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768673 | |||||||
| chr1:156768789 | C | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+550C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768789 | |||||||
| chr1:156768884 | G | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.468+645G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768884 | |||||||
| chr1:156768943 | C | A | 2 | a0002c0002t0001g0074 a0002c0002t0001g0075 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.468+704C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768943 | |||||||
| chr1:156768962 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.468+723C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156768962 | |||||||
| chr1:156769052 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.468+813C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769052 | |||||||
| chr1:156769261 | A | T | 1 | a0002c0002t0001g0257 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.468+1022A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769261 | |||||||
| chr1:156769299 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.468+1060T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769299 | |||||||
| chr1:156769326 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0322 a0001c0001t0001g0323 others(4): Show |
8 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1087C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769326 | |||||||
| chr1:156769382 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.468+1143G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769382 | |||||||
| chr1:156769591 | T | A | 34 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(31): Show |
35 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+1352T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769591 | |||||||
| chr1:156769598 | T | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+1359T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769598 | |||||||
| chr1:156769602 | T | A | 1 | a0001c0001t0004g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.468+1363T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769602 | |||||||
| chr1:156769630 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.468+1391C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769630 | |||||||
| chr1:156769716 | CAGCCTCT others(5): Show |
C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+1481_468+1492d others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156769716 | ||||||
| chr1:156769748 | C | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0001c0001t0001g0297 others(3): Show |
7 | HG00609.hp2 HG00673.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+1509C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769748 | |||||||
| chr1:156769857 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(97): Show |
111 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.468+1618C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769857 | |||||||
| chr1:156769992 | A | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+1753A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156769992 | |||||||
| chr1:156770206 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.468+1967A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770206 | |||||||
| chr1:156770234 | G | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0069 |
3 | HG01168.hp2 HG01169.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.468+1995G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770234 | |||||||
| chr1:156770616 | C | G | 24 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(21): Show |
24 | HG02602.hp2 HG02630.hp2 HG02698.hp1 others(21): Show |
intron_variant | MODIFIER | c.468+2377C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770616 | |||||||
| chr1:156770642 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.468+2403C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770642 | |||||||
| chr1:156770710 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | NA18964.hp2 NA18988.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.468+2471T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770710 | |||||||
| chr1:156770736 | A | G | 20 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(17): Show |
20 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.468+2497A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770736 | |||||||
| chr1:156770793 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.468+2554G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770793 | |||||||
| chr1:156770828 | A | G | 1 | a0001c0001t0004g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.468+2589A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770828 | |||||||
| chr1:156770863 | C | T | 58 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(55): Show |
59 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.468+2624C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770863 | |||||||
| chr1:156770996 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
6 | HG00408.hp1 HG02027.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+2757G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156770996 | |||||||
| chr1:156771063 | A | T | 1 | a0001c0001t0005g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.468+2824A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771063 | |||||||
| chr1:156771079 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(94): Show |
108 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.468+2840T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771079 | |||||||
| chr1:156771080 | G | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(94): Show |
108 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.468+2841G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771080 | |||||||
| chr1:156771195 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.468+2956A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771195 | |||||||
| chr1:156771376 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+3137G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771376 | |||||||
| chr1:156771449 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.468+3210T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771449 | |||||||
| chr1:156771562 | C | G | 3 | a0001c0001t0001g0302 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02257.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.468+3323C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771562 | |||||||
| chr1:156771635 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.468+3396G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771635 | |||||||
| chr1:156771682 | T | TG | 114 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0076 others(111): Show |
117 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.468+3444dupG | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156771682 | ||||||
| chr1:156771683 | G | GT | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
225 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.468+3456dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156771683 | ||||||
| chr1:156771705 | T | A | 6 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+3466T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771705 | |||||||
| chr1:156771791 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(95): Show |
109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.468+3552A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771791 | |||||||
| chr1:156771875 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01261.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.468+3636G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156771875 | |||||||
| chr1:156772145 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.468+3906C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156772145 | |||||||
| chr1:156772178 | C | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+3939C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156772178 | |||||||
| chr1:156772457 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.468+4218C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156772457 | |||||||
| chr1:156772620 | A | G | 1 | a0002c0002t0001g0257 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.468+4381A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156772620 | |||||||
| chr1:156772770 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.468+4531T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156772770 | |||||||
| chr1:156772817 | C | T | 1 | a0002c0002t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.468+4578C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156772817 | |||||||
| chr1:156772866 | G | A | 20 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(17): Show |
20 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.468+4627G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156772866 | |||||||
| chr1:156773137 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.468+4898T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773137 | |||||||
| chr1:156773157 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.468+4918G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773157 | |||||||
| chr1:156773166 | T | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0078 others(26): Show |
30 | HG02559.hp2 HG02602.hp2 HG02630.hp2 others(27): Show |
intron_variant | MODIFIER | c.468+4927T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773166 | |||||||
| chr1:156773176 | G | T | 6 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+4937G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773176 | |||||||
| chr1:156773178 | G | A | 1 | a0002c0002t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.468+4939G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773178 | |||||||
| chr1:156773368 | G | T | 1 | a0001c0007t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+5129G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773368 | |||||||
| chr1:156773381 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(91): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.468+5142G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773381 | |||||||
| chr1:156773382 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.468+5143G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773382 | |||||||
| chr1:156773479 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.468+5240C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773479 | |||||||
| chr1:156773501 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
5 | HG02109.hp2 HG02717.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+5262A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773501 | |||||||
| chr1:156773565 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.468+5326C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773565 | |||||||
| chr1:156773566 | G | C | 1 | a0001c0001t0001g0254 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.468+5327G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773566 | |||||||
| chr1:156773749 | AC | A | 4 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(1): Show |
4 | HG02622.hp1 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+5511delC | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156773749 | |||||||
| chr1:156774131 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.468+5892G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774131 | |||||||
| chr1:156774134 | GTTTC | G | 20 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(17): Show |
20 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.468+5903_468+5906d others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774134 | ||||||
| chr1:156774155 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.468+5916A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774155 | |||||||
| chr1:156774156 | CCTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.468+5918_468+5931d others(16): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774156 | |||||||
| chr1:156774157 | C | CT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(22): Show |
27 | HG00609.hp2 HG00639.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.468+5954dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0078 others(33): Show |
36 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+5953_468+5954d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTT | 41 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(38): Show |
41 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.468+5952_468+5954d others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTTT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(25): Show |
33 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.468+5951_468+5954d others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTTTT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0081 others(12): Show |
17 | HG00609.hp1 HG00642.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+5950_468+5954d others(7): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0236 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.468+5945_468+5954d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.468+5943_468+5954d others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.468+5942_468+5954d others(15): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.468+5939_468+5954d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.468+5938_468+5954d others(19): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CT | C | 6 | a0001c0001t0001g0107 a0001c0001t0001g0188 a0001c0001t0001g0189 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+5954delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTT | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.468+5952_468+5954d others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT | C | 12 | a0002c0002t0001g0113 a0002c0002t0001g0114 a0002c0002t0001g0118 others(9): Show |
12 | HG00733.hp1 HG01109.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.468+5948_468+5954d others(9): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(1): Show |
C | 34 | a0001c0001t0001g0135 a0001c0001t0001g0216 a0001c0001t0001g0311 others(31): Show |
35 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.468+5947_468+5954d others(10): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(2): Show |
C | 10 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0313 others(7): Show |
10 | HG01496.hp2 HG02809.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+5946_468+5954d others(11): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0213 a0001c0001t0001g0319 |
3 | HG02970.hp1 HG03017.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.468+5945_468+5954d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(4): Show |
C | 12 | a0001c0001t0001g0123 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
12 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.468+5944_468+5954d others(13): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.468+5943_468+5954d others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.468+5942_468+5954d others(15): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0129 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+5941_468+5954d others(16): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774157 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0231 |
2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.468+5939_468+5954d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774157 | ||||||
| chr1:156774163 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+5924T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774163 | |||||||
| chr1:156774171 | T | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.468+5932T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774171 | |||||||
| chr1:156774172 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.468+5933T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774172 | |||||||
| chr1:156774180 | T | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.468+5941T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774180 | |||||||
| chr1:156774181 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.468+5942T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774181 | |||||||
| chr1:156774262 | G | A | 3 | a0001c0001t0001g0302 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02257.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.468+6023G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774262 | |||||||
| chr1:156774408 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.468+6169C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774408 | |||||||
| chr1:156774420 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.468+6181G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774420 | |||||||
| chr1:156774427 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.468+6188G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774427 | |||||||
| chr1:156774521 | C | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0076 others(31): Show |
36 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+6282C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774521 | |||||||
| chr1:156774528 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.468+6289C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774528 | |||||||
| chr1:156774550 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.468+6311G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774550 | |||||||
| chr1:156774577 | C | T | 1 | a0002c0002t0001g0164 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.468+6338C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774577 | |||||||
| chr1:156774613 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.468+6374A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774613 | |||||||
| chr1:156774662 | A | G | 2 | a0002c0002t0001g0074 a0002c0002t0001g0075 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.468+6423A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774662 | |||||||
| chr1:156774843 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.468+6604T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774843 | |||||||
| chr1:156774881 | G | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG00544.hp2 HG00597.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+6642G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774881 | |||||||
| chr1:156774905 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(92): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.468+6666C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774905 | |||||||
| chr1:156774945 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.468+6706T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156774945 | |||||||
| chr1:156774950 | C | CA | 10 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
10 | HG00741.hp1 HG02738.hp2 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+6727dupA | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774950 | ||||||
| chr1:156774950 | CA | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(83): Show |
97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.468+6727delA | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156774950 | ||||||
| chr1:156775009 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.468+6770G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775009 | |||||||
| chr1:156775019 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.468+6780T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775019 | |||||||
| chr1:156775038 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.468+6799G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775038 | |||||||
| chr1:156775112 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.468+6873G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775112 | |||||||
| chr1:156775153 | CAGG | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+6917_468+6919d others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156775153 | ||||||
| chr1:156775172 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.468+6933C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775172 | |||||||
| chr1:156775228 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.468+6989G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775228 | |||||||
| chr1:156775237 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+6998G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775237 | |||||||
| chr1:156775355 | G | GT | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-6915dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156775355 | ||||||
| chr1:156775377 | G | T | 1 | a0001c0001t0001g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.469-6905G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775377 | |||||||
| chr1:156775415 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-6867A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775415 | |||||||
| chr1:156775426 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-6856C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775426 | |||||||
| chr1:156775485 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.469-6797G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775485 | |||||||
| chr1:156775512 | A | AT | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(92): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.469-6754dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156775512 | ||||||
| chr1:156775678 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
49 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.469-6604T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775678 | |||||||
| chr1:156775686 | T | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
6 | NA18944.hp1 NA18963.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-6596T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775686 | |||||||
| chr1:156775707 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(192): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.469-6575C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775707 | |||||||
| chr1:156775801 | AC | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0031 others(3): Show |
7 | HG00438.hp2 NA18944.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-6478delC | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156775801 | ||||||
| chr1:156775895 | T | G | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-6387T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156775895 | |||||||
| chr1:156776326 | C | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.469-5956C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156776326 | |||||||
| chr1:156776463 | TAG | T | 85 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(82): Show |
87 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.469-5816_469-5815d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156776463 | ||||||
| chr1:156776465 | GA | G | 3 | a0002c0002t0001g0114 a0002c0002t0001g0164 a0002c0002t0007g0115 |
3 | NA18961.hp2 NA18978.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.469-5816delA | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156776465 | |||||||
| chr1:156776468 | G | GT | 60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.469-5804dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156776468 | ||||||
| chr1:156776468 | G | T | 3 | a0002c0002t0001g0114 a0002c0002t0001g0164 a0002c0002t0007g0115 |
3 | NA18961.hp2 NA18978.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.469-5814G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156776468 | |||||||
| chr1:156776477 | T | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01891.hp2 HG02258.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-5805T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156776477 | |||||||
| chr1:156776585 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.469-5697A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156776585 | |||||||
| chr1:156776816 | G | A | 88 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(85): Show |
90 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.469-5466G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156776816 | |||||||
| chr1:156777111 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.469-5171G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156777111 | |||||||
| chr1:156777263 | T | TCCCGCAA others(3): Show |
1 | a0002c0002t0002g0163 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.469-5017_469-5008d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156777263 | ||||||
| chr1:156777346 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.469-4936C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156777346 | |||||||
| chr1:156777397 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.469-4885A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156777397 | |||||||
| chr1:156777735 | G | C | 1 | a0001c0001t0001g0301 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.469-4547G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156777735 | |||||||
| chr1:156777957 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
5 | HG02109.hp2 HG02717.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-4325A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156777957 | |||||||
| chr1:156778036 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(92): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.469-4246C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778036 | |||||||
| chr1:156778042 | T | C | 6 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-4240T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778042 | |||||||
| chr1:156778073 | C | G | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
54 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.469-4209C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778073 | |||||||
| chr1:156778157 | G | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.469-4125G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778157 | |||||||
| chr1:156778171 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.469-4111T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778171 | |||||||
| chr1:156778393 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.469-3889T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778393 | |||||||
| chr1:156778581 | C | CT | 7 | a0001c0001t0001g0162 a0001c0001t0001g0260 a0001c0001t0001g0262 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-3682dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156778581 | ||||||
| chr1:156778581 | CT | C | 30 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0076 others(27): Show |
30 | HG01167.hp1 HG01169.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.469-3682delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156778581 | ||||||
| chr1:156778602 | T | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.469-3680T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778602 | |||||||
| chr1:156778603 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.469-3679G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778603 | |||||||
| chr1:156778707 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.469-3575T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778707 | |||||||
| chr1:156778808 | A | AT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.469-3465dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156778808 | ||||||
| chr1:156778808 | A | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0311 a0001c0001t0003g0310 others(1): Show |
4 | HG00642.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-3474A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778808 | |||||||
| chr1:156778856 | A | G | 18 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(15): Show |
18 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.469-3426A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778856 | |||||||
| chr1:156778857 | T | C | 1 | a0001c0001t0005g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.469-3425T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778857 | |||||||
| chr1:156778913 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.469-3369C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156778913 | |||||||
| chr1:156779021 | A | G | 1 | a0002c0002t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.469-3261A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779021 | |||||||
| chr1:156779099 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.469-3183G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779099 | |||||||
| chr1:156779103 | A | AAT | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0174 others(2): Show |
5 | HG01433.hp1 HG03130.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-3154_469-3153d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATAT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0079 others(9): Show |
13 | HG00558.hp2 HG00738.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-3156_469-3153d others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATAT | 13 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0083 others(10): Show |
13 | HG00140.hp2 HG00438.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-3158_469-3153d others(8): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(1): Show |
6 | a0001c0001t0001g0103 a0001c0001t0001g0127 a0001c0001t0001g0129 others(3): Show |
6 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-3160_469-3153d others(10): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(3): Show |
5 | a0001c0001t0001g0102 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-3162_469-3153d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(5): Show |
1 | a0002c0002t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.469-3164_469-3153d others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(7): Show |
5 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0121 others(2): Show |
5 | HG01106.hp2 HG01168.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-3166_469-3153d others(16): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(9): Show |
3 | a0001c0001t0001g0077 a0001c0001t0001g0306 a0002c0002t0001g0257 |
3 | HG02451.hp2 HG02922.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.469-3168_469-3153d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(17): Show |
1 | a0002c0002t0001g0114 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.469-3176_469-3153d others(26): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0327 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.469-3153_469-3152i others(30): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779103 | A | AATATATA others(25): Show |
3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02896.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.469-3153_469-3152i others(34): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779103 | ||||||
| chr1:156779114 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.469-3166_469-3149d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779114 | ||||||
| chr1:156779116 | ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.469-3164_469-3140d others(27): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779116 | ||||||
| chr1:156779124 | ATATATTT others(8): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.469-3156_469-3142d others(17): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779124 | ||||||
| chr1:156779124 | ATATATTT others(9): Show |
A | 1 | a0001c0001t0001g0014 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.469-3156_469-3141d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779124 | ||||||
| chr1:156779124 | ATATATTT others(10): Show |
A | 4 | a0001c0001t0001g0287 a0002c0002t0001g0158 a0002c0002t0001g0159 others(1): Show |
4 | HG01071.hp2 HG01261.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-3156_469-3140d others(19): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779124 | ||||||
| chr1:156779124 | ATATATTT others(11): Show |
A | 5 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0001c0001t0001g0292 others(2): Show |
5 | HG02280.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-3156_469-3139d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779124 | ||||||
| chr1:156779126 | ATATTTTT | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0029 others(3): Show |
6 | HG02083.hp1 HG04184.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-3154_469-3148d others(9): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779126 | ||||||
| chr1:156779126 | ATATTTTT others(8): Show |
A | 6 | a0001c0001t0001g0258 a0001c0001t0001g0271 a0001c0001t0001g0273 others(3): Show |
6 | HG01175.hp2 HG01361.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-3154_469-3140d others(17): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779126 | ||||||
| chr1:156779126 | ATATTTTT others(9): Show |
A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0275 a0001c0001t0001g0296 others(4): Show |
7 | HG00609.hp2 HG00673.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-3154_469-3139d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779126 | ||||||
| chr1:156779126 | ATATTTTT others(10): Show |
A | 3 | a0001c0001t0001g0285 a0001c0001t0006g0295 a0002c0002t0001g0161 |
3 | HG02622.hp1 HG03209.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.469-3154_469-3138d others(19): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779126 | ||||||
| chr1:156779126 | ATATTTTT others(11): Show |
A | 13 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0267 others(10): Show |
13 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-3154_469-3137d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779126 | ||||||
| chr1:156779128 | AT | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0110 a0001c0001t0001g0172 others(8): Show |
11 | HG02132.hp2 HG02523.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.469-3123delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATT | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(49): Show |
62 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.469-3124_469-3123d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTT | A | 7 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG00280.hp2 HG01169.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-3125_469-3123d others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTT | A | 16 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0035 others(13): Show |
16 | HG00735.hp2 HG01934.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.469-3127_469-3123d others(7): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTTTT | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0019 others(21): Show |
25 | HG00408.hp1 HG00639.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.469-3129_469-3123d others(9): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTTTT others(1): Show |
A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(5): Show |
8 | HG01169.hp2 HG02080.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-3130_469-3123d others(10): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-3132_469-3123d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.469-3136_469-3123d others(16): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTTTT others(8): Show |
A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0262 others(3): Show |
9 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-3137_469-3123d others(17): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0261 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.469-3138_469-3123d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779128 | ATTTTTTT others(11): Show |
A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0278 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.469-3140_469-3123d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779128 | ||||||
| chr1:156779129 | T | TA | 9 | a0001c0001t0001g0109 a0001c0001t0001g0171 a0001c0001t0001g0181 others(6): Show |
9 | HG00544.hp2 HG00609.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-3153_469-3152i others(3): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATA | 14 | a0001c0001t0001g0015 a0001c0001t0001g0094 a0001c0001t0001g0097 others(11): Show |
14 | HG00735.hp1 HG01081.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.469-3153_469-3152i others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATA | 8 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0080 others(5): Show |
8 | HG00733.hp1 HG00741.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-3153_469-3152i others(7): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA | 5 | a0001c0001t0001g0093 a0001c0001t0001g0153 a0001c0001t0001g0162 others(2): Show |
5 | HG01109.hp1 HG02723.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-3153_469-3152i others(9): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(2): Show |
9 | a0002c0002t0001g0009 a0002c0002t0001g0136 a0002c0002t0001g0137 others(6): Show |
9 | HG01192.hp2 HG01952.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-3153_469-3152i others(11): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(4): Show |
3 | a0002c0002t0001g0075 a0002c0002t0001g0133 a0002c0002t0001g0165 |
3 | HG01070.hp1 HG02622.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.469-3153_469-3152i others(13): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(6): Show |
2 | a0002c0002t0001g0139 a0002c0002t0001g0143 |
2 | HG01074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.469-3153_469-3152i others(15): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(8): Show |
2 | a0002c0002t0001g0144 a0002c0002t0002g0163 |
2 | HG01255.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.469-3153_469-3152i others(17): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(12): Show |
2 | a0002c0002t0001g0116 a0002c0002t0001g0151 |
2 | NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.469-3153_469-3152i others(21): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(14): Show |
1 | a0002c0002t0001g0145 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.469-3153_469-3152i others(23): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(16): Show |
2 | a0001c0001t0001g0307 a0001c0001t0001g0321 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.469-3153_469-3152i others(25): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779129 | T | TATATATA others(18): Show |
3 | a0001c0001t0001g0255 a0002c0002t0001g0164 a0002c0002t0007g0115 |
3 | NA18961.hp2 NA18998.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.469-3153_469-3152i others(27): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779129 | |||||||
| chr1:156779130 | T | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(59): Show |
62 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.469-3152T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779130 | |||||||
| chr1:156779131 | T | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0093 others(64): Show |
70 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.469-3151T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779131 | |||||||
| chr1:156779132 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(97): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.469-3150T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779132 | |||||||
| chr1:156779133 | T | A | 71 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0093 others(68): Show |
74 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.469-3149T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779133 | |||||||
| chr1:156779134 | T | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(92): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.469-3148T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779134 | |||||||
| chr1:156779135 | T | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(74): Show |
80 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.469-3147T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779135 | |||||||
| chr1:156779136 | T | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(72): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.469-3146T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779136 | |||||||
| chr1:156779137 | T | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(62): Show |
68 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.469-3145T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779137 | |||||||
| chr1:156779138 | T | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0123 others(46): Show |
51 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.469-3144T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779138 | |||||||
| chr1:156779139 | T | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0109 others(46): Show |
51 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.469-3143T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779139 | |||||||
| chr1:156779140 | T | A | 36 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0124 others(33): Show |
36 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.469-3142T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779140 | |||||||
| chr1:156779141 | T | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0110 others(29): Show |
34 | HG00544.hp1 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.469-3141T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779141 | |||||||
| chr1:156779142 | T | A | 22 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0124 others(19): Show |
22 | HG00280.hp1 HG00597.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-3140T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779142 | |||||||
| chr1:156779143 | T | A | 14 | a0001c0001t0001g0135 a0001c0001t0001g0162 a0001c0001t0001g0198 others(11): Show |
14 | HG00741.hp1 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.469-3139T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779143 | |||||||
| chr1:156779144 | T | A | 7 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0002c0002t0001g0113 others(4): Show |
7 | HG00738.hp2 HG02074.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-3138T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779144 | |||||||
| chr1:156779144 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.469-3138T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779144 | |||||||
| chr1:156779145 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.469-3137T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779145 | |||||||
| chr1:156779151 | T | G | 3 | a0003c0003t0001g0045 a0003c0003t0001g0046 a0003c0003t0001g0064 |
3 | HG00639.hp1 HG01243.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.469-3131T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779151 | |||||||
| chr1:156779183 | C | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-3099C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779183 | |||||||
| chr1:156779339 | T | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(193): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.469-2943T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779339 | |||||||
| chr1:156779461 | G | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0175 a0001c0001t0001g0176 others(13): Show |
17 | HG00140.hp1 HG00738.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.469-2821G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779461 | |||||||
| chr1:156779521 | G | A | 2 | a0001c0001t0001g0033 a0006c0009t0001g0050 |
2 | HG03654.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.469-2761G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779521 | |||||||
| chr1:156779535 | C | CTAA | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.469-2746_469-2745i others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779535 | ||||||
| chr1:156779558 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.469-2724G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779558 | |||||||
| chr1:156779635 | C | A | 18 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(15): Show |
18 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.469-2647C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779635 | |||||||
| chr1:156779740 | C | A | 20 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(17): Show |
20 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.469-2542C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779740 | |||||||
| chr1:156779767 | T | TG | 10 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2508dupG | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779767 | ||||||
| chr1:156779825 | T | C | 1 | a0001c0001t0001g0010 | 2 | NA19065.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.469-2457T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779825 | |||||||
| chr1:156779862 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.469-2420C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779862 | |||||||
| chr1:156779896 | A | AT | 11 | a0001c0001t0001g0002 a0001c0001t0001g0101 a0001c0001t0001g0186 others(8): Show |
13 | HG00621.hp1 HG01884.hp1 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-2373dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 156779896 | ||||||
| chr1:156779976 | C | T | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
140 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.469-2306C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156779976 | |||||||
| chr1:156780008 | A | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(45): Show |
52 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.469-2274A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780008 | |||||||
| chr1:156780096 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0226 |
2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.469-2186G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780096 | |||||||
| chr1:156780182 | C | T | 1 | a0002c0002t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.469-2100C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780182 | |||||||
| chr1:156780209 | C | T | 1 | a0001c0007t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.469-2073C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780209 | |||||||
| chr1:156780339 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.469-1943G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780339 | |||||||
| chr1:156780391 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.469-1891T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780391 | |||||||
| chr1:156780392 | A | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0078 others(26): Show |
30 | HG02559.hp2 HG02602.hp2 HG02630.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-1890A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780392 | |||||||
| chr1:156780402 | T | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0078 others(26): Show |
30 | HG02559.hp2 HG02602.hp2 HG02630.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-1880T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780402 | |||||||
| chr1:156780406 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.469-1876T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780406 | |||||||
| chr1:156780607 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1675C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780607 | |||||||
| chr1:156780707 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.469-1575C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780707 | |||||||
| chr1:156780798 | G | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.469-1484G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780798 | |||||||
| chr1:156780847 | C | T | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1435C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156780847 | |||||||
| chr1:156781017 | T | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.469-1265T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781017 | |||||||
| chr1:156781019 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.469-1263C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781019 | |||||||
| chr1:156781020 | G | A | 1 | a0003c0003t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.469-1262G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781020 | |||||||
| chr1:156781023 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.469-1259C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781023 | |||||||
| chr1:156781039 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.469-1243T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781039 | |||||||
| chr1:156781057 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.469-1225G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781057 | |||||||
| chr1:156781127 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.469-1155C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781127 | |||||||
| chr1:156781285 | A | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.469-997A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781285 | |||||||
| chr1:156781330 | C | T | 1 | a0001c0001t0008g0063 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.469-952C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781330 | |||||||
| chr1:156781372 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.469-910G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781372 | |||||||
| chr1:156781455 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.469-827G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781455 | |||||||
| chr1:156781524 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.469-758T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781524 | |||||||
| chr1:156781526 | G | T | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-756G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781526 | |||||||
| chr1:156781527 | C | A | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-755C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781527 | |||||||
| chr1:156781528 | G | A | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-754G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781528 | |||||||
| chr1:156781529 | G | T | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-753G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781529 | |||||||
| chr1:156781530 | C | G | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-752C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781530 | |||||||
| chr1:156781532 | C | T | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-750C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781532 | |||||||
| chr1:156781533 | T | A | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-749T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781533 | |||||||
| chr1:156781534 | C | G | 1 | a0002c0002t0007g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.469-748C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781534 | |||||||
| chr1:156781767 | A | G | 1 | a0002c0002t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.469-515A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781767 | |||||||
| chr1:156781834 | G | T | 24 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(21): Show |
24 | HG02602.hp2 HG02630.hp2 HG02698.hp1 others(21): Show |
intron_variant | MODIFIER | c.469-448G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156781834 | |||||||
| chr1:156782198 | C | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-84C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156782198 | |||||||
| chr1:156782256 | C | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(193): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.469-26C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 1/6 | chr1 | 156782256 | |||||||
| chr1:156782346 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0065 |
2 | NA18998.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.516+17A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782346 | |||||||
| chr1:156782405 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.516+76C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782405 | |||||||
| chr1:156782431 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.516+102A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782431 | |||||||
| chr1:156782439 | AT | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(193): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.516+113delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156782439 | ||||||
| chr1:156782444 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.516+115A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782444 | |||||||
| chr1:156782460 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.516+131G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782460 | |||||||
| chr1:156782578 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(44): Show |
52 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.516+249T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782578 | |||||||
| chr1:156782727 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.516+398T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782727 | |||||||
| chr1:156782767 | A | G | 1 | a0002c0002t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.516+438A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782767 | |||||||
| chr1:156782791 | C | T | 3 | a0003c0003t0001g0045 a0003c0003t0001g0046 a0003c0003t0001g0064 |
3 | HG00639.hp1 HG01243.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.516+462C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782791 | |||||||
| chr1:156782820 | T | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(99): Show |
114 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.516+491T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782820 | |||||||
| chr1:156782912 | A | T | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.516+583A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782912 | |||||||
| chr1:156782914 | T | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0110 others(12): Show |
16 | HG00140.hp1 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.516+585T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156782914 | |||||||
| chr1:156783050 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.516+721A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783050 | |||||||
| chr1:156783065 | C | T | 94 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0072 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.516+736C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783065 | |||||||
| chr1:156783068 | C | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+739C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783068 | |||||||
| chr1:156783193 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.516+864C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783193 | |||||||
| chr1:156783442 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.516+1113C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783442 | |||||||
| chr1:156783517 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1188G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783517 | |||||||
| chr1:156783532 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.516+1203A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783532 | |||||||
| chr1:156783591 | C | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0131 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+1262C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783591 | |||||||
| chr1:156783607 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.516+1278G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783607 | |||||||
| chr1:156783621 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1292C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783621 | |||||||
| chr1:156783636 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.516+1307C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783636 | |||||||
| chr1:156783660 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.516+1331C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783660 | |||||||
| chr1:156783778 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1449A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783778 | |||||||
| chr1:156783947 | A | AT | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
151 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.516+1631dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156783947 | ||||||
| chr1:156783962 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.516+1633G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783962 | |||||||
| chr1:156783963 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.516+1634G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783963 | |||||||
| chr1:156783967 | G | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
49 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.516+1638G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156783967 | |||||||
| chr1:156784068 | T | C | 3 | a0001c0001t0001g0302 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02257.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+1739T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784068 | |||||||
| chr1:156784125 | T | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1796T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784125 | |||||||
| chr1:156784149 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.516+1820G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784149 | |||||||
| chr1:156784222 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.516+1893T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784222 | |||||||
| chr1:156784239 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0131 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+1910G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784239 | |||||||
| chr1:156784307 | C | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.516+1978C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784307 | |||||||
| chr1:156784325 | G | C | 6 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0271 others(3): Show |
6 | HG00639.hp2 HG01175.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+1996G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784325 | |||||||
| chr1:156784329 | C | G | 3 | a0002c0002t0001g0139 a0002c0002t0001g0147 a0002c0002t0001g0148 |
3 | HG01074.hp2 HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.516+2000C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784329 | |||||||
| chr1:156784381 | A | T | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+2052A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784381 | |||||||
| chr1:156784486 | G | A | 87 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(84): Show |
89 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.517-2122G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784486 | |||||||
| chr1:156784508 | T | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.517-2100T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784508 | |||||||
| chr1:156784673 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.517-1935T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156784673 | |||||||
| chr1:156785009 | C | CAT | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
49 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.517-1587_517-1586d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156785009 | ||||||
| chr1:156785009 | C | CATAT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0291 a0001c0001t0001g0324 others(2): Show |
6 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-1589_517-1586d others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156785009 | ||||||
| chr1:156785036 | C | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-1572C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785036 | |||||||
| chr1:156785042 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
6 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-1566A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785042 | |||||||
| chr1:156785047 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.517-1561A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785047 | |||||||
| chr1:156785108 | ATGTCT | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-1498_517-1494d others(7): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156785108 | ||||||
| chr1:156785109 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.517-1499T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785109 | |||||||
| chr1:156785310 | G | A | 24 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(21): Show |
24 | HG02602.hp2 HG02630.hp2 HG02698.hp1 others(21): Show |
intron_variant | MODIFIER | c.517-1298G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785310 | |||||||
| chr1:156785375 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.517-1233G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785375 | |||||||
| chr1:156785401 | C | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.517-1207C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785401 | |||||||
| chr1:156785592 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.517-1016G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785592 | |||||||
| chr1:156785596 | GA | G | 58 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(55): Show |
59 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.517-1004delA | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156785596 | ||||||
| chr1:156785597 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-1011A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785597 | |||||||
| chr1:156785629 | GC | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
49 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.517-978delC | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785629 | |||||||
| chr1:156785724 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-884C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785724 | |||||||
| chr1:156785757 | T | G | 18 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(15): Show |
18 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.517-851T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785757 | |||||||
| chr1:156785762 | C | T | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-846C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785762 | |||||||
| chr1:156785815 | C | CT | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.517-779dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156785815 | ||||||
| chr1:156785815 | C | CTT | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.517-780_517-779dup others(2): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 156785815 | ||||||
| chr1:156785986 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.517-622A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785986 | |||||||
| chr1:156785993 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.517-615A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156785993 | |||||||
| chr1:156786106 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.517-502C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156786106 | |||||||
| chr1:156786111 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.517-497G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156786111 | |||||||
| chr1:156786415 | C | T | 16 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(13): Show |
16 | HG02602.hp2 HG02738.hp1 HG03710.hp1 others(13): Show |
intron_variant | MODIFIER | c.517-193C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 2/6 | chr1 | 156786415 | |||||||
| chr1:156787262 | T | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+88T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787262 | |||||||
| chr1:156787371 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1083+197C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787371 | |||||||
| chr1:156787409 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1083+235T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787409 | |||||||
| chr1:156787410 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1083+236A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787410 | |||||||
| chr1:156787446 | G | GATAT | 3 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0070 |
3 | HG02145.hp2 HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1083+274_1083+275i others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787446 | GATTGATA others(3): Show |
G | 1 | a0001c0001t0001g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1083+275_1083+284d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787446 | GATTGATA others(7): Show |
G | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1083+275_1083+288d others(16): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787446 | GATTGATA others(9): Show |
G | 1 | a0001c0001t0001g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1083+275_1083+290d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787446 | GATTGATA others(11): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1083+275_1083+292d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787446 | GATTGATA others(15): Show |
G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0003c0003t0001g0045 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083+275_1083+296d others(24): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787446 | GATTGATA others(17): Show |
G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(38): Show |
44 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1083+275_1083+298d others(26): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787446 | GATTGATA others(19): Show |
G | 1 | a0001c0001t0001g0040 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1083+275_1083+300d others(28): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787446 | ||||||
| chr1:156787449 | T | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+275T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787449 | |||||||
| chr1:156787449 | TGATATAT others(17): Show |
T | 4 | a0002c0002t0001g0113 a0002c0002t0001g0138 a0002c0002t0001g0154 others(1): Show |
4 | HG02523.hp1 NA18941.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+276_1083+299d others(26): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787449 | |||||||
| chr1:156787450 | G | GATATAT | 3 | a0001c0001t0001g0313 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02809.hp1 HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1083+319_1083+324d others(8): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | G | GATATATA others(9): Show |
1 | a0001c0001t0001g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1083+309_1083+324d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | G | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+276G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787450 | |||||||
| chr1:156787450 | GATATATA others(1): Show |
G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0311 |
4 | HG02717.hp1 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+317_1083+324d others(10): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(3): Show |
G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0320 |
2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1083+315_1083+324d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(5): Show |
G | 1 | a0001c0001t0001g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1083+313_1083+324d others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(7): Show |
G | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG02486.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+311_1083+324d others(16): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(11): Show |
G | 1 | a0001c0001t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1083+307_1083+324d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(13): Show |
G | 5 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0131 others(2): Show |
5 | HG01099.hp2 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083+305_1083+324d others(22): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(15): Show |
G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
53 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1083+303_1083+324d others(24): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(17): Show |
G | 45 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0135 others(42): Show |
46 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1083+301_1083+324d others(26): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(19): Show |
G | 14 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(11): Show |
14 | HG00280.hp2 HG02027.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1083+299_1083+324d others(28): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787450 | GATATATA others(21): Show |
G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(119): Show |
135 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1083+297_1083+324d others(30): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787450 | ||||||
| chr1:156787452 | T | G | 1 | a0001c0007t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1083+278T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787452 | |||||||
| chr1:156787476 | T | G | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1083+302T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787476 | |||||||
| chr1:156787491 | ATATATAT others(1): Show |
A | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG02615.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+319_1083+326d others(10): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787491 | ||||||
| chr1:156787499 | C | A | 1 | a0001c0001t0003g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1083+325C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787499 | |||||||
| chr1:156787501 | GT | G | 88 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(85): Show |
90 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1083+336delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787501 | ||||||
| chr1:156787622 | C | CATAGTAC others(9): Show |
317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.1083+450_1083+465d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787622 | ||||||
| chr1:156787650 | C | CTT | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG02486.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+491_1083+492d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTT | 42 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0076 others(39): Show |
45 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1083+488_1083+492d others(7): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTC others(5): Show |
1 | a0001c0001t0001g0230 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1083+482_1083+483i others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+484_1083+492d others(11): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0052 |
2 | HG02145.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1083+483_1083+492d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(4): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(38): Show |
44 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+482_1083+492d others(13): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(5): Show |
132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(129): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1083+481_1083+492d others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(6): Show |
54 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0093 others(51): Show |
54 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1083+480_1083+492d others(15): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(7): Show |
11 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0125 others(8): Show |
11 | HG00280.hp1 HG01099.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1083+479_1083+492d others(16): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(15): Show |
3 | a0001c0001t0001g0260 a0001c0001t0001g0281 a0001c0001t0001g0301 |
3 | HG01109.hp2 HG01891.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1083+492_1083+493i others(24): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(16): Show |
6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+492_1083+493i others(25): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(18): Show |
5 | a0001c0001t0001g0072 a0001c0001t0001g0269 a0001c0001t0001g0292 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+492_1083+493i others(27): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(19): Show |
2 | a0001c0001t0001g0294 a0001c0001t0001g0309 |
2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1083+492_1083+493i others(28): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0006g0295 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1083+492_1083+493i others(29): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1083+492_1083+493i others(32): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787650 | C | CTTTTTTT others(32): Show |
1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1083+492_1083+493i others(41): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787650 | ||||||
| chr1:156787736 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1083+562T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787736 | |||||||
| chr1:156787819 | C | CTAATTTT others(2740): Show |
1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1083+661_1083+662i others(2749): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787819 | ||||||
| chr1:156787854 | C | T | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 |
3 | HG02723.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1083+680C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787854 | |||||||
| chr1:156787855 | G | A | 59 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(56): Show |
60 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1083+681G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787855 | |||||||
| chr1:156787862 | T | TG | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+689dupG | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156787862 | ||||||
| chr1:156787888 | G | C | 1 | a0001c0007t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1083+714G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787888 | |||||||
| chr1:156787941 | C | G | 1 | a0002c0002t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1083+767C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156787941 | |||||||
| chr1:156788083 | G | A | 6 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+909G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788083 | |||||||
| chr1:156788110 | A | G | 3 | a0001c0001t0001g0286 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1083+936A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788110 | |||||||
| chr1:156788134 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1083+960T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788134 | |||||||
| chr1:156788364 | G | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+1190G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788364 | |||||||
| chr1:156788407 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1083+1233G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788407 | |||||||
| chr1:156788545 | T | C | 89 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(86): Show |
91 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1083+1371T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788545 | |||||||
| chr1:156788659 | CT | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
237 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1083+1506delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156788659 | ||||||
| chr1:156788659 | CTT | C | 18 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(15): Show |
18 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.1083+1505_1083+150 others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 156788659 | ||||||
| chr1:156788810 | C | T | 88 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(85): Show |
90 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1083+1636C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788810 | |||||||
| chr1:156788880 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1083+1706G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156788880 | |||||||
| chr1:156789072 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
51 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1083+1898C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789072 | |||||||
| chr1:156789188 | T | A | 1 | a0002c0002t0001g0113 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1083+2014T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789188 | |||||||
| chr1:156789233 | G | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+2059G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789233 | |||||||
| chr1:156789261 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1083+2087T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789261 | |||||||
| chr1:156789471 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1084-2226G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789471 | |||||||
| chr1:156789489 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1084-2208T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789489 | |||||||
| chr1:156789793 | G | A | 94 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0072 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1084-1904G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789793 | |||||||
| chr1:156789847 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1084-1850A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789847 | |||||||
| chr1:156789853 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1084-1844G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789853 | |||||||
| chr1:156789962 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1084-1735G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156789962 | |||||||
| chr1:156790024 | A | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-1673A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156790024 | |||||||
| chr1:156790099 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1084-1598T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156790099 | |||||||
| chr1:156790244 | G | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(193): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1084-1453G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156790244 | |||||||
| chr1:156790701 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1084-996A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156790701 | |||||||
| chr1:156790748 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1084-949A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156790748 | |||||||
| chr1:156790749 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1084-948T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156790749 | |||||||
| chr1:156790963 | T | C | 17 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(14): Show |
17 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.1084-734T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156790963 | |||||||
| chr1:156791095 | C | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(88): Show |
102 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1084-602C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156791095 | |||||||
| chr1:156791224 | C | T | 8 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG02615.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-473C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156791224 | |||||||
| chr1:156791455 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1084-242C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156791455 | |||||||
| chr1:156791628 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1084-69A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | chr1 | 156791628 | |||||||
| chr1:156791826 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
59 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1179+34C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156791826 | |||||||
| chr1:156791856 | C | T | 3 | a0001c0001t0001g0302 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02257.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1179+64C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156791856 | |||||||
| chr1:156792053 | C | CT | 60 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): Show |
65 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.1179+289dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTT | 59 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0092 others(56): Show |
60 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1179+288_1179+289d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTT | 13 | a0001c0001t0001g0123 a0001c0001t0001g0162 a0001c0001t0001g0285 others(10): Show |
13 | HG00735.hp1 HG01106.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1179+287_1179+289d others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0004g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1179+280_1179+289d others(12): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG00741.hp2 HG01884.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+279_1179+289d others(13): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0041 |
2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1179+277_1179+289d others(15): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0042 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1179+274_1179+289d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0051 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1179+272_1179+289d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1179+270_1179+289d others(22): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1179+269_1179+289d others(23): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0019 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1179+267_1179+289d others(25): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(19): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0059 |
2 | HG02080.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1179+264_1179+289d others(28): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0017 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1179+263_1179+289d others(29): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(21): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0060 |
2 | NA18980.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1179+262_1179+289d others(30): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(22): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0003c0003t0001g0045 |
3 | HG02735.hp1 NA18964.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1179+289_1179+290i others(31): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0048 |
2 | HG02738.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1179+289_1179+290i others(32): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0066 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1179+289_1179+290i others(33): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0021 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1179+289_1179+290i others(34): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0065 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1179+289_1179+290i others(36): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0022 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1179+289_1179+290i others(37): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(29): Show |
1 | a0006c0009t0001g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1179+289_1179+290i others(38): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | C | CTTTTTTT others(33): Show |
1 | a0008c0005t0001g0061 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1179+289_1179+290i others(42): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | CT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(87): Show |
101 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1179+289delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | CTT | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0189 others(13): Show |
16 | HG01192.hp1 HG02257.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1179+288_1179+289d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | CTTTT | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0028 others(8): Show |
12 | HG00438.hp2 HG02165.hp1 HG04184.hp1 others(9): Show |
intron_variant | MODIFIER | c.1179+286_1179+289d others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+277_1179+289d others(15): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792053 | CTTTTTTT others(10): Show |
C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179+273_1179+289d others(19): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156792053 | ||||||
| chr1:156792126 | C | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(99): Show |
114 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1179+334C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792126 | |||||||
| chr1:156792191 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.1179+399A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792191 | |||||||
| chr1:156792487 | G | A | 3 | a0001c0001t0001g0302 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02257.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1179+695G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792487 | |||||||
| chr1:156792626 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179+834G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792626 | |||||||
| chr1:156792642 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1179+850C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792642 | |||||||
| chr1:156792677 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1179+885A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792677 | |||||||
| chr1:156792701 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1179+909C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792701 | |||||||
| chr1:156792798 | A | C | 94 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0076 others(91): Show |
97 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1179+1006A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156792798 | |||||||
| chr1:156793318 | G | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-1347G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793318 | |||||||
| chr1:156793489 | TG | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
49 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1180-1173delG | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156793489 | ||||||
| chr1:156793493 | CT | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0102 others(4): Show |
8 | HG02451.hp2 HG02559.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180-1158delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156793493 | ||||||
| chr1:156793494 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1180-1171T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793494 | |||||||
| chr1:156793503 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1180-1162T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793503 | |||||||
| chr1:156793541 | ACT | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
6 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-1121_1180-112 others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156793541 | ||||||
| chr1:156793648 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1180-1017G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793648 | |||||||
| chr1:156793824 | C | G | 1 | a0001c0001t0006g0295 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1180-841C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793824 | |||||||
| chr1:156793839 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1180-826G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793839 | |||||||
| chr1:156793893 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1180-772C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793893 | |||||||
| chr1:156793907 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1180-758G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156793907 | |||||||
| chr1:156793954 | CT | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
207 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.1180-692delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156793954 | ||||||
| chr1:156793954 | CTT | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(117): Show |
132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1180-693_1180-692d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 156793954 | ||||||
| chr1:156794059 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-606G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156794059 | |||||||
| chr1:156794073 | T | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-592T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156794073 | |||||||
| chr1:156794177 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1180-488G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156794177 | |||||||
| chr1:156794246 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(194): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1180-419T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156794246 | |||||||
| chr1:156794385 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1180-280G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156794385 | |||||||
| chr1:156794485 | A | C | 17 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(14): Show |
17 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.1180-180A>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 4/6 | chr1 | 156794485 | |||||||
| chr1:156795059 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1323+251C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795059 | |||||||
| chr1:156795125 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(99): Show |
114 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1323+317G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795125 | |||||||
| chr1:156795170 | C | T | 1 | a0002c0002t0001g0113 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1323+362C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795170 | |||||||
| chr1:156795285 | G | GT | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(41): Show |
47 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1323+501dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTGTTTTT others(11): Show |
1 | a0001c0001t0001g0299 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1323+478_1323+479i others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0031 others(13): Show |
16 | HG00438.hp2 HG00735.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1323+500_1323+501d others(4): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTT | 26 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(23): Show |
27 | HG00733.hp1 HG01081.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1323+498_1323+501d others(6): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTT | 51 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0084 others(48): Show |
52 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1323+497_1323+501d others(7): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTT | 11 | a0001c0001t0001g0124 a0001c0001t0001g0260 a0002c0002t0001g0118 others(8): Show |
11 | HG00544.hp1 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1323+496_1323+501d others(8): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0279 |
6 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+490_1323+491i others(19): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(11): Show |
3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0277 |
3 | HG01934.hp1 NA18973.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1323+490_1323+491i others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(9): Show |
2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1323+486_1323+501d others(18): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(10): Show |
7 | a0001c0001t0001g0270 a0001c0001t0001g0291 a0001c0001t0001g0292 others(4): Show |
7 | HG00609.hp2 HG02083.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1323+485_1323+501d others(19): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(11): Show |
13 | a0001c0001t0001g0014 a0001c0001t0001g0265 a0001c0001t0001g0267 others(10): Show |
14 | HG00673.hp1 HG01261.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1323+484_1323+501d others(20): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(12): Show |
2 | a0001c0001t0001g0264 a0001c0001t0001g0269 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1323+483_1323+501d others(21): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(13): Show |
4 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0001g0271 others(1): Show |
4 | HG00639.hp2 HG01361.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+482_1323+501d others(22): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(14): Show |
1 | a0001c0001t0001g0288 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1323+481_1323+501d others(23): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1323+478_1323+501d others(26): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(18): Show |
1 | a0001c0001t0001g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1323+501_1323+502i others(27): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(19): Show |
2 | a0001c0001t0001g0258 a0001c0001t0001g0273 |
2 | HG01175.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1323+501_1323+502i others(28): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(23): Show |
1 | a0001c0001t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1323+501_1323+502i others(32): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | G | GTTTTTTT others(27): Show |
2 | a0001c0001t0001g0276 a0001c0001t0001g0278 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1323+501_1323+502i others(36): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | GT | G | 9 | a0001c0001t0001g0101 a0001c0001t0001g0302 a0001c0001t0001g0304 others(6): Show |
9 | HG01884.hp1 HG02257.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1323+501delT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795285 | GTTT | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(91): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1323+499_1323+501d others(5): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 156795285 | ||||||
| chr1:156795341 | G | T | 1 | a0002c0002t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1323+533G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795341 | |||||||
| chr1:156795390 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1323+582T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795390 | |||||||
| chr1:156795424 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1323+616G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795424 | |||||||
| chr1:156795513 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1323+705C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795513 | |||||||
| chr1:156795592 | A | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
42 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1323+784A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795592 | |||||||
| chr1:156795595 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1323+787T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795595 | |||||||
| chr1:156795677 | A | G | 3 | a0001c0001t0001g0302 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02257.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1323+869A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795677 | |||||||
| chr1:156795724 | C | A | 1 | a0002c0002t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1323+916C>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795724 | |||||||
| chr1:156795725 | C | G | 1 | a0002c0002t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1323+917C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156795725 | |||||||
| chr1:156796001 | G | C | 4 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(1): Show |
4 | HG02622.hp1 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+1193G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796001 | |||||||
| chr1:156796040 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1323+1232C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796040 | |||||||
| chr1:156796041 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1233A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796041 | |||||||
| chr1:156796181 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(193): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1324-1095C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796181 | |||||||
| chr1:156796209 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1324-1067T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796209 | |||||||
| chr1:156796241 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0131 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324-1035G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796241 | |||||||
| chr1:156796453 | G | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02258.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-823G>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796453 | |||||||
| chr1:156796706 | G | A | 1 | a0002c0002t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1324-570G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796706 | |||||||
| chr1:156796823 | T | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(2): Show |
5 | HG02630.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-453T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796823 | |||||||
| chr1:156796882 | C | G | 2 | a0002c0002t0001g0143 a0002c0002t0001g0145 |
2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1324-394C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156796882 | |||||||
| chr1:156797201 | A | G | 3 | a0002c0002t0001g0139 a0002c0002t0001g0147 a0002c0002t0001g0148 |
3 | HG01074.hp2 HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1324-75A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 5/6 | chr1 | 156797201 | |||||||
| chr1:156797461 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
49 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1389+120C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156797461 | |||||||
| chr1:156797812 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1389+471T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156797812 | |||||||
| chr1:156797879 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1389+538C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156797879 | |||||||
| chr1:156797933 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1389+592C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156797933 | |||||||
| chr1:156797951 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1389+610T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156797951 | |||||||
| chr1:156797952 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1389+611C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156797952 | |||||||
| chr1:156798096 | A | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1389+755A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798096 | |||||||
| chr1:156798210 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1389+869T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798210 | |||||||
| chr1:156798268 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1389+927C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798268 | |||||||
| chr1:156798510 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1389+1169T>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798510 | |||||||
| chr1:156798774 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0183 |
3 | NA18965.hp1 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1389+1433G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798774 | |||||||
| chr1:156798776 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
6 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+1435G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798776 | |||||||
| chr1:156798803 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1389+1462C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798803 | |||||||
| chr1:156798840 | C | CAAAA | 6 | a0001c0001t0001g0302 a0001c0001t0001g0311 a0001c0001t0001g0319 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1389+1515_1390-151 others(8): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 156798840 | ||||||
| chr1:156798840 | CA | C | 23 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0070 others(20): Show |
23 | HG00280.hp1 HG01099.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1390-1515delA | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 156798840 | ||||||
| chr1:156798840 | CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1389+1509_1390-151 others(14): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 156798840 | ||||||
| chr1:156798919 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(138): Show |
147 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1390-1455A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156798919 | |||||||
| chr1:156799143 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1390-1231G>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156799143 | |||||||
| chr1:156799357 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(100): Show |
115 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1390-1017T>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156799357 | |||||||
| chr1:156799371 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1390-1003T>A | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156799371 | |||||||
| chr1:156799582 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1390-792C>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156799582 | |||||||
| chr1:156799803 | G | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1390-571G>C | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156799803 | |||||||
| chr1:156799915 | G | GT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1390-458dupT | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 156799915 | ||||||
| chr1:156799993 | A | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1390-381A>T | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156799993 | |||||||
| chr1:156800124 | C | G | 4 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0121 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-250C>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156800124 | |||||||
| chr1:156800183 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1390-191A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156800183 | |||||||
| chr1:156800262 | A | G | 6 | a0001c0001t0001g0179 a0001c0001t0001g0203 a0001c0001t0001g0206 others(3): Show |
6 | HG00423.hp1 HG02040.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1390-112A>G | PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 6/6 | chr1 | 156800262 |