Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5096 |
| ensemblid | ENSG00000114054.14 |
| hgncid | 8654 |
| symbol | PCCB |
| name | propionyl-CoA carboxylase subunit beta |
| refseq_nuc | NM_000532.5 |
| refseq_prot | NP_000523.2 |
| ensembl_nuc | ENST00000251654.9 |
| ensembl_prot | ENSP00000251654.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 136250340 |
| end | 136330169 |
| strand | + |
| ver | v1.2 |
| region | chr3:136250340-136330169 |
| region5000 | chr3:136245340-136335169 |
| regionname0 | PCCB_chr3_136250340_136330169 |
| regionname5000 | PCCB_chr3_136245340_136335169 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 539 | 293 | 85 | 57 | 105 | 10 | 34 | 79 | PCCB_chr3_136245340_136335169 | PCCB | MAAAL others(534): Show |
chr3 | 136245340 | 136335169 |
| a0002 | 0/0 | 539 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | MAAAL others(534): Show |
chr3 | 136245340 | 136335169 |
| a0003 | 0/0 | 539 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | MAAAL others(534): Show |
chr3 | 136245340 | 136335169 |
| a0004 | 0/0 | 539 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | MAAAL others(534): Show |
chr3 | 136245340 | 136335169 |
| a0005 | 0/0 | 539 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | MAAAL others(534): Show |
chr3 | 136245340 | 136335169 |
| a0006 | 0/0 | 539 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | MAAAL others(534): Show |
chr3 | 136245340 | 136335169 |
| a0007 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | MAAAL others(540): Show |
chr3 | 136245340 | 136335169 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1617 | 290 | 84 | 56 | 105 | 9 | 34 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0001c0002 | 0/0 | 1617 | 2 | 1 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0001c0009 | 0/0 | 1617 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0002c0003 | 0/0 | 1617 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0003c0007 | 0/0 | 1617 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0004c0005 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0005c0008 | 0/0 | 1617 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0006c0006 | 0/0 | 1617 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1612): Show |
chr3 | 136245340 | 136335169 | ||
| a0007c0004 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | ATGGC others(1630): Show |
chr3 | 136245340 | 136335169 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1799 | 287 | 81 | 56 | 105 | 9 | 34 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0001c0001t0002 | 0/0 | 1799 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0001c0001t0003 | 0/0 | 1799 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0001c0002t0001 | 0/0 | 1799 | 2 | 1 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0001c0009t0001 | 0/0 | 1799 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0002c0003t0001 | 0/0 | 1799 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0003c0007t0001 | 0/0 | 1799 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0004c0005t0001 | 0/0 | 1799 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0005c0008t0001 | 0/0 | 1799 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0006c0006t0001 | 0/0 | 1799 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1794): Show |
chr3 | 136245340 | 136335169 |
| a0007c0004t0001 | 0/0 | 1817 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | AGGTG others(1812): Show |
chr3 | 136245340 | 136335169 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0001c0009t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0002c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0003c0007t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0004c0005t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0005c0008t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0006c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| a0007c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0009 | t0001 | g0114 | EUR | GBR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01358 | hp1 | a0003 | c0007 | t0001 | g0223 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CDX | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0207 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03209 | hp2 | a0004 | c0005 | t0001 | g0286 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03491 | hp2 | a0005 | c0008 | t0001 | g0231 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03831 | hp2 | a0006 | c0006 | t0001 | g0118 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19057 | hp1 | a0007 | c0004 | t0001 | g0087 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0191 | REF | REF | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0210 | REF | REF | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136250376 | A | ATGGCGGC others(11): Show |
1 | a0007 | 1 | NA19057.hp1 | disruptive_inframe_insertion | MODERATE | c.11_28dupCATTACGGGT others(8): Show |
p.Ala4_Ala9dup | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/15 | 65/1799 | 29/1620 | 10/539 | INFO_REALIGN_3_PRIME | chr3 | 136250376 | ||
| chr3:136256589 | G | A | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.338G>A | p.Arg113Gln | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/15 | 374/1799 | 338/1620 | 113/539 | chr3 | 136256589 | |||
| chr3:136297962 | C | G | 1 | a0002 | 2 | HG02886.hp2 HG03041.hp2 |
missense_variant | MODERATE | c.774C>G | p.His258Gln | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/15 | 810/1799 | 774/1620 | 258/539 | chr3 | 136297962 | |||
| chr3:136327686 | C | T | 1 | a0005 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1352C>T | p.Thr451Ile | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/15 | 1388/1799 | 1352/1620 | 451/539 | chr3 | 136327686 | |||
| chr3:136327706 | G | A | 1 | a0006 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.1372G>A | p.Ala458Thr | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/15 | 1408/1799 | 1372/1620 | 458/539 | chr3 | 136327706 | |||
| chr3:136328849 | C | T | 1 | a0003 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1490C>T | p.Ala497Val | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/15 | 1526/1799 | 1490/1620 | 497/539 | chr3 | 136328849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136283839 | G | A | 1 | a0001c0002 | 2 | HG00735.hp1 NA19240.hp2 |
splice_region_variant&synonymous_variant | LOW | c.546G>A | p.Arg182Arg | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/15 | 582/1799 | 546/1620 | 182/539 | chr3 | 136283839 | |||
| chr3:136283905 | C | T | 1 | a0001c0009 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.612C>T | p.Ala204Ala | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/15 | 648/1799 | 612/1620 | 204/539 | chr3 | 136283905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136330070 | C | T | 1 | a0001c0001t0003 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 15/15 | 44 | chr3 | 136330070 | ||||||
| chr3:136330117 | C | A | 1 | a0001c0001t0002 | 2 | HG03139.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*91C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 15/15 | 91 | chr3 | 136330117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136250613 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+55T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250613 | |||||||
| chr3:136250663 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.183+105C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250663 | |||||||
| chr3:136250695 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+137G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250695 | |||||||
| chr3:136250705 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.183+147A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250705 | |||||||
| chr3:136250759 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+201T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250759 | |||||||
| chr3:136250821 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+263A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250821 | |||||||
| chr3:136250913 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.183+355T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250913 | |||||||
| chr3:136251087 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.183+529G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251087 | |||||||
| chr3:136251116 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.183+558C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251116 | |||||||
| chr3:136251335 | A | G | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+777A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251335 | |||||||
| chr3:136251356 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+798G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251356 | |||||||
| chr3:136251438 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.183+880C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251438 | |||||||
| chr3:136251646 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+1088A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251646 | |||||||
| chr3:136251862 | C | A | 19 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
19 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.183+1304C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251862 | |||||||
| chr3:136252438 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
11 | HG00544.hp1 HG00609.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+1880A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252438 | |||||||
| chr3:136252526 | A | AT | 6 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(3): Show |
6 | HG00597.hp2 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+1983dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252526 | ||||||
| chr3:136252526 | AT | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+1983delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252526 | ||||||
| chr3:136252662 | A | AT | 36 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(33): Show |
37 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+2125dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252662 | ||||||
| chr3:136252695 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+2137G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252695 | |||||||
| chr3:136252695 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.183+2137G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252695 | |||||||
| chr3:136252851 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.183+2293C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252851 | |||||||
| chr3:136252907 | TG | T | 20 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(17): Show |
20 | HG00280.hp2 HG00733.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.183+2350delG | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252907 | |||||||
| chr3:136252908 | G | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG00741.hp2 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+2350G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252908 | |||||||
| chr3:136252908 | GT | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
176 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.183+2363delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252908 | ||||||
| chr3:136252961 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+2403A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252961 | |||||||
| chr3:136253008 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.183+2450C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253008 | |||||||
| chr3:136253015 | G | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2457G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253015 | |||||||
| chr3:136253082 | G | GT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0032 others(34): Show |
39 | HG00597.hp2 HG00642.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.183+2549dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | ||||||
| chr3:136253082 | G | GTT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
110 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.183+2548_183+2549d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | ||||||
| chr3:136253082 | G | GTTT | 25 | a0001c0001t0001g0016 a0001c0001t0001g0124 a0001c0001t0001g0125 others(22): Show |
25 | HG00423.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.183+2547_183+2549d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | ||||||
| chr3:136253082 | GTTTTT | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2545_183+2549d others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | ||||||
| chr3:136253086 | T | TTTG | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01433.hp1 HG02300.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2530_183+2531i others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253086 | ||||||
| chr3:136253087 | T | TTG | 21 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(18): Show |
21 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.183+2530_183+2531i others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253087 | ||||||
| chr3:136253088 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2530T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253088 | |||||||
| chr3:136253150 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.183+2592C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253150 | |||||||
| chr3:136253279 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.184-2577C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253279 | |||||||
| chr3:136253325 | G | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.184-2531G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253325 | |||||||
| chr3:136253439 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0140 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-2417C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253439 | |||||||
| chr3:136253566 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.184-2290G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253566 | |||||||
| chr3:136253585 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.184-2271A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253585 | |||||||
| chr3:136253664 | A | AT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-2171dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253664 | ||||||
| chr3:136253664 | AT | A | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
9 | HG00099.hp2 HG00544.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-2171delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253664 | ||||||
| chr3:136253755 | C | T | 42 | a0001c0001t0001g0201 a0001c0001t0001g0224 a0001c0001t0001g0225 others(39): Show |
42 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.184-2101C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253755 | |||||||
| chr3:136253952 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.184-1904T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253952 | |||||||
| chr3:136254012 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.184-1844A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254012 | |||||||
| chr3:136254080 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.184-1776T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254080 | |||||||
| chr3:136254208 | C | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-1648C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254208 | |||||||
| chr3:136254309 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1547C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254309 | |||||||
| chr3:136254326 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0123 others(2): Show |
6 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-1530C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254326 | |||||||
| chr3:136254366 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1490G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254366 | |||||||
| chr3:136254462 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-1394C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254462 | |||||||
| chr3:136254515 | T | G | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.184-1341T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254515 | |||||||
| chr3:136254518 | C | CT | 30 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(27): Show |
30 | HG00733.hp1 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.184-1308dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | C | CTT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0052 others(18): Show |
22 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.184-1309_184-1308d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | C | CTTT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(54): Show |
60 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.184-1310_184-1308d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | C | CTTTT | 38 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0048 others(35): Show |
38 | HG00621.hp2 HG00735.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.184-1311_184-1308d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | C | CTTTTT | 11 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG00099.hp1 HG01928.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-1312_184-1308d others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | CT | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0142 others(46): Show |
50 | HG00280.hp1 HG00280.hp2 HG01361.hp1 others(47): Show |
intron_variant | MODIFIER | c.184-1308delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | CTT | C | 9 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0225 others(6): Show |
9 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-1309_184-1308d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.184-1317_184-1308d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0183 |
3 | HG02109.hp1 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.184-1318_184-1308d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.184-1321_184-1308d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254518 | CTTTTTTT others(8): Show |
C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0033 |
2 | HG00735.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.184-1322_184-1308d others(17): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | ||||||
| chr3:136254536 | TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1319_184-1307d others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254536 | |||||||
| chr3:136254549 | A | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0292 a0001c0001t0002g0046 others(1): Show |
4 | HG03139.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1307A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254549 | |||||||
| chr3:136254668 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.184-1188G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254668 | |||||||
| chr3:136254713 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.184-1143C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254713 | |||||||
| chr3:136254786 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.184-1070C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254786 | |||||||
| chr3:136254816 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0221 |
2 | HG01496.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.184-1040C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254816 | |||||||
| chr3:136254830 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1026C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254830 | |||||||
| chr3:136254878 | CTT | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-965_184-964del others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254878 | ||||||
| chr3:136254946 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.184-910G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254946 | |||||||
| chr3:136255027 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.184-829C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255027 | |||||||
| chr3:136255076 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-780A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255076 | |||||||
| chr3:136255212 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.184-644T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255212 | |||||||
| chr3:136255309 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.184-547A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255309 | |||||||
| chr3:136255322 | G | C | 1 | a0001c0001t0001g0120 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.184-534G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255322 | |||||||
| chr3:136255374 | G | A | 20 | a0001c0001t0001g0037 a0001c0001t0001g0142 a0001c0001t0001g0143 others(17): Show |
20 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-482G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255374 | |||||||
| chr3:136255385 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.184-471G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255385 | |||||||
| chr3:136255628 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.184-228A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255628 | |||||||
| chr3:136255718 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.184-138G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255718 | |||||||
| chr3:136255769 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-87C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255769 | |||||||
| chr3:136255785 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-71A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255785 | |||||||
| chr3:136256408 | T | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.304-147T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 2/14 | chr3 | 136256408 | |||||||
| chr3:136256519 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304-36G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 2/14 | chr3 | 136256519 | |||||||
| chr3:136256654 | T | C | 14 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0093 others(11): Show |
14 | HG00621.hp2 HG02080.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.372+31T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136256654 | |||||||
| chr3:136256908 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.372+285G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136256908 | |||||||
| chr3:136256908 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.372+285G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136256908 | |||||||
| chr3:136257240 | G | T | 1 | a0001c0001t0001g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.372+617G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257240 | |||||||
| chr3:136257285 | A | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0140 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+662A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257285 | |||||||
| chr3:136257521 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA18959.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.372+898C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257521 | |||||||
| chr3:136257622 | C | T | 8 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(5): Show |
8 | HG02165.hp2 HG02523.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+999C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257622 | |||||||
| chr3:136257907 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.372+1284T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257907 | |||||||
| chr3:136257982 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.372+1359G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257982 | |||||||
| chr3:136257991 | A | ATGCATTT others(11): Show |
1 | a0001c0001t0001g0179 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.372+1370_372+1387d others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136257991 | ||||||
| chr3:136258075 | A | ATTTC | 62 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
62 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.372+1455_372+1456i others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136258075 | ||||||
| chr3:136258126 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0002g0046 others(2): Show |
5 | HG01496.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1503C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258126 | |||||||
| chr3:136258137 | GAGAT | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+1518_372+1521d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136258137 | ||||||
| chr3:136258167 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1544A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258167 | |||||||
| chr3:136258198 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.372+1575G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258198 | |||||||
| chr3:136258335 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+1712C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258335 | |||||||
| chr3:136258463 | A | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0217 a0001c0001t0001g0218 others(3): Show |
6 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+1840A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258463 | |||||||
| chr3:136258571 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.373-1908T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258571 | |||||||
| chr3:136258599 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.373-1880G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258599 | |||||||
| chr3:136259187 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1292C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259187 | |||||||
| chr3:136259248 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.373-1231C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259248 | |||||||
| chr3:136259250 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0279 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.373-1229T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259250 | |||||||
| chr3:136259310 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.373-1169C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259310 | |||||||
| chr3:136259357 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.373-1122C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259357 | |||||||
| chr3:136259396 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.373-1083C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259396 | |||||||
| chr3:136259397 | G | A | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.373-1082G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259397 | |||||||
| chr3:136259470 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG00544.hp1 HG01496.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.373-1009G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259470 | |||||||
| chr3:136259601 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.373-878T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259601 | |||||||
| chr3:136259783 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-696C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259783 | |||||||
| chr3:136259813 | A | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-666A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259813 | |||||||
| chr3:136259955 | T | C | 20 | a0001c0001t0001g0037 a0001c0001t0001g0142 a0001c0001t0001g0143 others(17): Show |
20 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.373-524T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259955 | |||||||
| chr3:136260031 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-448T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260031 | |||||||
| chr3:136260057 | T | TTTTTG | 5 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
6 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-391_373-387dup others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | ||||||
| chr3:136260057 | TTTTTG | T | 14 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0205 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-391_373-387del others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | ||||||
| chr3:136260057 | TTTTTGTT others(3): Show |
T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.373-396_373-387del others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | ||||||
| chr3:136260057 | TTTTTGTT others(8): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.373-401_373-387del others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | ||||||
| chr3:136260223 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | NA18953.hp2 NA18964.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.373-256G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260223 | |||||||
| chr3:136260306 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
7 | HG01243.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.373-173G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260306 | |||||||
| chr3:136260355 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.373-124G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260355 | |||||||
| chr3:136260592 | T | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.429+57T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260592 | |||||||
| chr3:136260663 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429+128C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260663 | |||||||
| chr3:136260842 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+307C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260842 | |||||||
| chr3:136260844 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+309A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260844 | |||||||
| chr3:136260856 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(109): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.429+321A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260856 | |||||||
| chr3:136260921 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.429+386C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260921 | |||||||
| chr3:136260936 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429+401A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260936 | |||||||
| chr3:136261027 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.429+492G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261027 | |||||||
| chr3:136261089 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(7): Show |
11 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+554C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261089 | |||||||
| chr3:136261137 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.429+602T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261137 | |||||||
| chr3:136261139 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.429+604T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261139 | |||||||
| chr3:136261221 | T | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0175 others(2): Show |
5 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+686T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261221 | |||||||
| chr3:136261349 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-603C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261349 | |||||||
| chr3:136261556 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.430-396A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261556 | |||||||
| chr3:136261578 | GA | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(67): Show |
72 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.430-371delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 136261578 | ||||||
| chr3:136261583 | T | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(67): Show |
72 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.430-369T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261583 | |||||||
| chr3:136261636 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00609.hp1 HG01884.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-316C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261636 | |||||||
| chr3:136261831 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(66): Show |
71 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.430-121C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261831 | |||||||
| chr3:136261879 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.430-73T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261879 | |||||||
| chr3:136262112 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.543+47C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262112 | |||||||
| chr3:136262177 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.543+112G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262177 | |||||||
| chr3:136262312 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.543+247A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262312 | |||||||
| chr3:136262470 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.543+405G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262470 | |||||||
| chr3:136262785 | G | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.543+720G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262785 | |||||||
| chr3:136262856 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG00544.hp1 HG01516.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+791C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262856 | |||||||
| chr3:136262940 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+875T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262940 | |||||||
| chr3:136262954 | G | GT | 18 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0045 others(15): Show |
18 | HG00621.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+907dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136262954 | ||||||
| chr3:136262954 | GT | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(97): Show |
102 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.543+907delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136262954 | ||||||
| chr3:136263079 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+1014C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263079 | |||||||
| chr3:136263219 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+1154C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263219 | |||||||
| chr3:136263254 | G | GT | 41 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0051 others(38): Show |
42 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.543+1206dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136263254 | ||||||
| chr3:136263254 | G | GTT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
201 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(198): Show |
intron_variant | MODIFIER | c.543+1205_543+1206d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136263254 | ||||||
| chr3:136263254 | G | GTTT | 47 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0001g0038 others(44): Show |
47 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.543+1204_543+1206d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136263254 | ||||||
| chr3:136263346 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.543+1281A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263346 | |||||||
| chr3:136263365 | A | C | 1 | a0006c0006t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.543+1300A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263365 | |||||||
| chr3:136263478 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+1413C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263478 | |||||||
| chr3:136263512 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.543+1447T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263512 | |||||||
| chr3:136263575 | A | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0001t0001g0202 others(42): Show |
46 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.543+1510A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263575 | |||||||
| chr3:136263641 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543+1576G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263641 | |||||||
| chr3:136263739 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+1674C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263739 | |||||||
| chr3:136263740 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+1675G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263740 | |||||||
| chr3:136263944 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0103 |
3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.543+1879A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263944 | |||||||
| chr3:136263972 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.543+1907A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263972 | |||||||
| chr3:136264011 | C | CA | 10 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG00423.hp2 HG01433.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.543+1962dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264011 | ||||||
| chr3:136264011 | CA | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(47): Show |
52 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.543+1962delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264011 | ||||||
| chr3:136264247 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+2182A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264247 | |||||||
| chr3:136264325 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0189 |
3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.543+2260C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264325 | |||||||
| chr3:136264396 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.543+2331G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264396 | |||||||
| chr3:136264417 | GTC | G | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.543+2357_543+2358d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264417 | ||||||
| chr3:136264430 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0048 |
2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.543+2365A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264430 | |||||||
| chr3:136264440 | G | GTGTATAT others(7): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0123 others(1): Show |
5 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(9): Show |
11 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0140 others(8): Show |
11 | HG01123.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(11): Show |
6 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0168 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(13): Show |
6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG00738.hp1 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(15): Show |
3 | a0001c0001t0001g0167 a0001c0001t0001g0172 a0001c0001t0001g0174 |
3 | HG01109.hp1 HG01255.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(24): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(17): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0176 |
4 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(19): Show |
1 | a0001c0001t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(28): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(21): Show |
1 | a0001c0001t0001g0050 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(30): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(23): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(32): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(25): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0197 a0001c0001t0001g0293 |
3 | HG00741.hp2 HG03239.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(34): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(27): Show |
1 | a0001c0001t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(36): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(29): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(38): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(31): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0157 |
2 | HG01346.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(40): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(33): Show |
4 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0154 others(1): Show |
4 | HG00280.hp2 HG00733.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(35): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0196 |
2 | HG01069.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(44): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATAT others(39): Show |
1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(48): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTATGT others(33): Show |
1 | a0001c0001t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTGTAT others(5): Show |
1 | a0001c0001t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTGTAT others(9): Show |
1 | a0001c0001t0001g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTGTAT others(35): Show |
1 | a0001c0001t0001g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(44): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTGTAT others(39): Show |
1 | a0001c0001t0001g0038 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(48): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTGTAT others(45): Show |
1 | a0001c0001t0001g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(54): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264440 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(24): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | ||||||
| chr3:136264442 | A | G | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+2377A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264442 | |||||||
| chr3:136264444 | ATATG | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+2383_543+2386d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264444 | ||||||
| chr3:136264448 | G | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0035 others(60): Show |
65 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.543+2383G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264448 | |||||||
| chr3:136264448 | G | GTA | 6 | a0001c0001t0001g0014 a0001c0001t0001g0203 a0001c0001t0001g0261 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+2395_543+2396d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | ||||||
| chr3:136264448 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG00544.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.543+2384_543+2385i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | ||||||
| chr3:136264448 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0009 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.543+2384_543+2385i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | ||||||
| chr3:136264448 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0008 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.543+2384_543+2385i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | ||||||
| chr3:136264448 | G | GTGTATAT others(13): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.543+2384_543+2385i others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | ||||||
| chr3:136264458 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+2393A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264458 | |||||||
| chr3:136264598 | G | C | 12 | a0001c0001t0001g0037 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG00733.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+2533G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264598 | |||||||
| chr3:136264655 | C | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0199 others(25): Show |
29 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.543+2590C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264655 | |||||||
| chr3:136264675 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0187 |
2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.543+2610C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264675 | |||||||
| chr3:136264710 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.543+2645A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264710 | |||||||
| chr3:136264874 | C | CA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(109): Show |
114 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.543+2830dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264874 | ||||||
| chr3:136264874 | C | CAA | 28 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0041 others(25): Show |
28 | HG00280.hp2 HG00597.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.543+2829_543+2830d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264874 | ||||||
| chr3:136264874 | CA | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.543+2830delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264874 | ||||||
| chr3:136264917 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+2852C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264917 | |||||||
| chr3:136264924 | G | A | 8 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0172 others(5): Show |
8 | HG00738.hp1 HG01109.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+2859G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264924 | |||||||
| chr3:136264955 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2890G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264955 | |||||||
| chr3:136265021 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2956C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265021 | |||||||
| chr3:136265028 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.543+2963T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265028 | |||||||
| chr3:136265219 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543+3154T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265219 | |||||||
| chr3:136265221 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+3156T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265221 | |||||||
| chr3:136265293 | T | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0137 a0001c0001t0001g0224 others(2): Show |
5 | HG02080.hp1 NA18986.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+3228T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265293 | |||||||
| chr3:136265300 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.543+3235A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265300 | |||||||
| chr3:136265581 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543+3516A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265581 | |||||||
| chr3:136265723 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.543+3658G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265723 | |||||||
| chr3:136265767 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.543+3702A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265767 | |||||||
| chr3:136265830 | G | GT | 20 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(17): Show |
20 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+3778dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136265830 | ||||||
| chr3:136265830 | GT | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+3778delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136265830 | ||||||
| chr3:136265927 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+3862G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265927 | |||||||
| chr3:136266124 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+4059A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266124 | |||||||
| chr3:136266131 | G | GT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(3): Show |
6 | HG01175.hp2 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+4081dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136266131 | ||||||
| chr3:136266133 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+4068T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266133 | |||||||
| chr3:136266415 | C | CACCGCAC others(151): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+4472_543+4473i others(160): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136266415 | ||||||
| chr3:136266584 | G | C | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543+4519G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266584 | |||||||
| chr3:136266982 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.543+4917A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266982 | |||||||
| chr3:136267083 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+5018C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267083 | |||||||
| chr3:136267245 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
202 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.543+5180A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267245 | |||||||
| chr3:136267596 | T | G | 29 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
29 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+5531T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267596 | |||||||
| chr3:136267702 | T | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+5637T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267702 | |||||||
| chr3:136267718 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+5653C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267718 | |||||||
| chr3:136267944 | C | CT | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(21): Show |
24 | HG00609.hp1 HG01255.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+5898dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136267944 | ||||||
| chr3:136267944 | C | CTT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+5897_543+5898d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136267944 | ||||||
| chr3:136267944 | CT | C | 12 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0068 others(9): Show |
12 | HG00323.hp2 HG00733.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+5898delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136267944 | ||||||
| chr3:136268065 | C | CGT | 105 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(102): Show |
106 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.543+6019_543+6020d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268065 | ||||||
| chr3:136268065 | C | CGTGT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0042 others(3): Show |
7 | HG02630.hp2 HG03041.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+6017_543+6020d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268065 | ||||||
| chr3:136268084 | G | GTGTGTAG others(3): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.543+6020_543+6021i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268084 | ||||||
| chr3:136268084 | G | GTGTGTAG others(11): Show |
1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.543+6020_543+6021i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268084 | ||||||
| chr3:136268085 | T | TGTGTAGA others(5): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.543+6020_543+6021i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268085 | |||||||
| chr3:136268085 | TAG | T | 23 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(20): Show |
23 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+6022_543+6023d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268085 | ||||||
| chr3:136268086 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0175 |
2 | HG01346.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.543+6021A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268086 | |||||||
| chr3:136268087 | G | GAGATATA others(5): Show |
1 | a0001c0001t0001g0230 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.543+6023_543+6024i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATAT | 8 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0205 others(5): Show |
8 | HG02145.hp1 HG02258.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+6053_543+6056d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATAGA others(3): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 |
3 | HG02895.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.543+6027_543+6028i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATAGA others(5): Show |
3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0030 |
3 | HG03486.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.543+6027_543+6028i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATAGA others(7): Show |
1 | a0001c0002t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.543+6027_543+6028i others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATAGA others(9): Show |
1 | a0001c0002t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.543+6027_543+6028i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATAGA others(11): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0025 |
2 | HG01243.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.543+6027_543+6028i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATAT | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
15 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+6051_543+6056d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(1): Show |
9 | a0001c0001t0001g0119 a0001c0001t0001g0140 a0001c0001t0001g0204 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+6049_543+6056d others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(3): Show |
10 | a0001c0001t0001g0035 a0001c0001t0001g0202 a0001c0001t0001g0228 others(7): Show |
10 | HG00323.hp1 HG00621.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+6047_543+6056d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(5): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0229 others(9): Show |
12 | HG01243.hp2 HG02080.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+6045_543+6056d others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(7): Show |
4 | a0001c0001t0001g0235 a0001c0001t0001g0238 a0001c0001t0001g0246 others(1): Show |
4 | HG00280.hp1 NA18952.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+6043_543+6056d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(9): Show |
4 | a0001c0001t0001g0216 a0001c0001t0001g0239 a0001c0001t0001g0247 others(1): Show |
4 | HG00597.hp2 HG01358.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+6041_543+6056d others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(11): Show |
2 | a0001c0001t0001g0254 a0001c0001t0001g0281 |
2 | NA18989.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.543+6039_543+6056d others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(15): Show |
2 | a0001c0001t0001g0251 a0001c0001t0001g0253 |
2 | NA18963.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.543+6035_543+6056d others(24): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | GATATATA others(5): Show |
1 | a0001c0001t0001g0236 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.543+6030_543+6031i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | G | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG01346.hp2 HG01891.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+6022G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268087 | |||||||
| chr3:136268087 | GAT | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
68 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.543+6055_543+6056d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | GATATAT | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0160 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+6051_543+6056d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | GATATATA others(1): Show |
G | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+6049_543+6056d others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | GATATATA others(3): Show |
G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0221 |
3 | HG01123.hp2 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.543+6047_543+6056d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | GATATATA others(7): Show |
G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.543+6043_543+6056d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | GATATATA others(9): Show |
G | 1 | a0001c0001t0001g0011 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.543+6041_543+6056d others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | GATATATA others(11): Show |
G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG02135.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+6039_543+6056d others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268087 | GATATATA others(29): Show |
G | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.543+6041_543+6076d others(38): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | ||||||
| chr3:136268088 | A | G | 25 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(22): Show |
25 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+6023A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268088 | |||||||
| chr3:136268090 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.543+6042_543+6043i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268090 | ||||||
| chr3:136268090 | A | G | 25 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(22): Show |
25 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+6025A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268090 | |||||||
| chr3:136268091 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0175 |
2 | HG01433.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.543+6026T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268091 | |||||||
| chr3:136268092 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.543+6027A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268092 | |||||||
| chr3:136268093 | T | G | 25 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(22): Show |
25 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+6028T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268093 | |||||||
| chr3:136268094 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0032 |
3 | HG01433.hp2 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.543+6044_543+6045i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268094 | ||||||
| chr3:136268094 | A | ATATATAT others(7): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+6042_543+6043i others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268094 | ||||||
| chr3:136268094 | A | ATATATG | 13 | a0001c0001t0001g0059 a0001c0001t0001g0093 a0001c0001t0001g0094 others(10): Show |
13 | HG00621.hp2 HG01255.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.543+6034_543+6035i others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268094 | ||||||
| chr3:136268095 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.543+6030T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268095 | |||||||
| chr3:136268095 | T | TATATATA others(5): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0258 |
2 | HG00423.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.543+6041_543+6042i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268095 | ||||||
| chr3:136268096 | A | ATATG | 19 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0071 others(16): Show |
19 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.543+6034_543+6035i others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268096 | ||||||
| chr3:136268096 | A | ATATGTAT others(23): Show |
1 | a0001c0001t0001g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.543+6034_543+6035i others(32): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268096 | ||||||
| chr3:136268097 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.543+6032T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268097 | |||||||
| chr3:136268098 | A | ATG | 3 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0158 |
3 | HG01928.hp1 HG02132.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.543+6034_543+6035i others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | ||||||
| chr3:136268098 | A | ATGTATAT others(21): Show |
1 | a0001c0001t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.543+6034_543+6035i others(30): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | ||||||
| chr3:136268098 | A | ATGTATAT others(41): Show |
1 | a0001c0001t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543+6034_543+6035i others(50): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | ||||||
| chr3:136268098 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0266 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+6053_543+6076d others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | ||||||
| chr3:136268099 | T | G | 24 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(21): Show |
24 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.543+6034T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268099 | |||||||
| chr3:136268100 | A | G | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0072 others(3): Show |
6 | HG00609.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+6035A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268100 | |||||||
| chr3:136268101 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.543+6036T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268101 | |||||||
| chr3:136268102 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(60): Show |
65 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.543+6037A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268102 | |||||||
| chr3:136268105 | T | TAC | 14 | a0001c0001t0001g0051 a0001c0001t0001g0200 a0001c0001t0001g0212 others(11): Show |
14 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+6041_543+6042i others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268105 | ||||||
| chr3:136268107 | T | C | 7 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+6042T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268107 | |||||||
| chr3:136268107 | T | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.543+6042T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268107 | |||||||
| chr3:136268116 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.543+6051A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268116 | |||||||
| chr3:136268120 | A | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0072 others(2): Show |
5 | HG00609.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+6055A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268120 | |||||||
| chr3:136268122 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
10 | HG00609.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+6057G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268122 | |||||||
| chr3:136268122 | G | GTA | 3 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0001g0098 |
3 | HG00621.hp2 HG02523.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.543+6075_543+6076d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268122 | ||||||
| chr3:136268124 | A | G | 8 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0175 others(5): Show |
8 | HG01496.hp1 HG01496.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+6059A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268124 | |||||||
| chr3:136268136 | A | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(79): Show |
84 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.543+6071A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268136 | |||||||
| chr3:136268314 | G | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0274 a0001c0001t0001g0283 others(1): Show |
5 | HG00642.hp2 HG01175.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+6249G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268314 | |||||||
| chr3:136268465 | G | GT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(99): Show |
104 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.543+6417dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268465 | ||||||
| chr3:136268465 | G | GTT | 11 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0089 others(8): Show |
11 | HG00323.hp2 HG01928.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+6416_543+6417d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268465 | ||||||
| chr3:136268543 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0279 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.543+6478A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268543 | |||||||
| chr3:136268564 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.543+6499A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268564 | |||||||
| chr3:136268890 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.543+6825G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268890 | |||||||
| chr3:136268899 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.543+6834T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268899 | |||||||
| chr3:136268964 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.543+6899C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268964 | |||||||
| chr3:136269113 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7048T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269113 | |||||||
| chr3:136269234 | G | C | 1 | a0001c0002t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.543+7169G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269234 | |||||||
| chr3:136269344 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.543+7279G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269344 | |||||||
| chr3:136269464 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7399C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269464 | |||||||
| chr3:136269570 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.543+7505G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269570 | |||||||
| chr3:136269607 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7542C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269607 | |||||||
| chr3:136269663 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+7598A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269663 | |||||||
| chr3:136269701 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0179 |
2 | NA18953.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.543+7636C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269701 | |||||||
| chr3:136269742 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+7677C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269742 | |||||||
| chr3:136269802 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.543+7737C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269802 | |||||||
| chr3:136269810 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543+7745C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269810 | |||||||
| chr3:136269815 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7750G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269815 | |||||||
| chr3:136269817 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.543+7752C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269817 | |||||||
| chr3:136269822 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0088 |
2 | HG00597.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.543+7757C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269822 | |||||||
| chr3:136269885 | C | CA | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG00544.hp1 HG00733.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+7842dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269885 | ||||||
| chr3:136269885 | CA | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0039 others(4): Show |
7 | HG01256.hp2 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+7842delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269885 | ||||||
| chr3:136269908 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.543+7843T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269908 | |||||||
| chr3:136269933 | C | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+7868C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269933 | |||||||
| chr3:136269993 | G | GT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(21): Show |
25 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.543+7944dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269993 | ||||||
| chr3:136269993 | GT | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.543+7944delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269993 | ||||||
| chr3:136269996 | T | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+7931T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269996 | |||||||
| chr3:136270052 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543+7987A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270052 | |||||||
| chr3:136270450 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
197 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.543+8385C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270450 | |||||||
| chr3:136270505 | A | T | 1 | a0001c0001t0001g0004 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.543+8440A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270505 | |||||||
| chr3:136270505 | AT | A | 20 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
20 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+8451delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136270505 | ||||||
| chr3:136270516 | T | TC | 3 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0155 |
3 | HG00280.hp2 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.543+8454dupC | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136270516 | ||||||
| chr3:136270534 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(77): Show |
82 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.543+8469C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270534 | |||||||
| chr3:136270566 | C | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0275 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.543+8501C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270566 | |||||||
| chr3:136270695 | A | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+8630A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270695 | |||||||
| chr3:136270697 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+8632G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270697 | |||||||
| chr3:136270713 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0285 |
2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.543+8648T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270713 | |||||||
| chr3:136270829 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.543+8764C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270829 | |||||||
| chr3:136270853 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0233 |
3 | HG02080.hp1 NA18986.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.543+8788A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270853 | |||||||
| chr3:136270863 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(42): Show |
47 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.543+8798G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270863 | |||||||
| chr3:136271386 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.543+9321A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271386 | |||||||
| chr3:136271398 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.543+9333A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271398 | |||||||
| chr3:136271558 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+9493T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271558 | |||||||
| chr3:136271689 | T | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+9624T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271689 | |||||||
| chr3:136271811 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+9746A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271811 | |||||||
| chr3:136271972 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.543+9907A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271972 | |||||||
| chr3:136272036 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543+9971C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272036 | |||||||
| chr3:136272039 | A | T | 29 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
29 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+9974A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272039 | |||||||
| chr3:136272046 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+9981G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272046 | |||||||
| chr3:136272301 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(24): Show |
29 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+10236A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272301 | |||||||
| chr3:136272431 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.543+10366T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272431 | |||||||
| chr3:136272600 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+10535T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272600 | |||||||
| chr3:136272732 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+10667A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272732 | |||||||
| chr3:136272905 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.543+10840C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272905 | |||||||
| chr3:136272927 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.543+10862C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272927 | |||||||
| chr3:136272966 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-10871T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272966 | |||||||
| chr3:136273160 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.544-10677C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273160 | |||||||
| chr3:136273417 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.544-10420C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273417 | |||||||
| chr3:136273547 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.544-10290C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273547 | |||||||
| chr3:136273578 | CTTTTTTT others(19): Show |
C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-10247_544-1022 others(30): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273578 | ||||||
| chr3:136273589 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-10248T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273589 | |||||||
| chr3:136273590 | CTTTTTTC others(3): Show |
C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-10240_544-1023 others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273590 | ||||||
| chr3:136273597 | C | CT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
55 | HG00597.hp2 HG00738.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.544-10218dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273597 | ||||||
| chr3:136273597 | C | CTT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0062 others(6): Show |
9 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-10219_544-1021 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273597 | ||||||
| chr3:136273597 | CT | C | 34 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(31): Show |
34 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.544-10218delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273597 | ||||||
| chr3:136273601 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.544-10236T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273601 | |||||||
| chr3:136273603 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0122 |
3 | HG02055.hp1 HG02074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-10234T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273603 | |||||||
| chr3:136273684 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18945.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.544-10153G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273684 | |||||||
| chr3:136273688 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.544-10149G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273688 | |||||||
| chr3:136273747 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.544-10090C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273747 | |||||||
| chr3:136273772 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-10065C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273772 | |||||||
| chr3:136273781 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.544-10056G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273781 | |||||||
| chr3:136273803 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.544-10034T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273803 | |||||||
| chr3:136273911 | C | CA | 13 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0214 others(10): Show |
13 | HG01167.hp1 HG01516.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-9901dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273911 | ||||||
| chr3:136273911 | CA | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(110): Show |
115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.544-9901delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273911 | ||||||
| chr3:136273911 | CAA | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(55): Show |
60 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.544-9902_544-9901d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273911 | ||||||
| chr3:136273994 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.544-9843C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273994 | |||||||
| chr3:136274058 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-9779T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274058 | |||||||
| chr3:136274093 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.544-9744C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274093 | |||||||
| chr3:136274228 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.544-9609G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274228 | |||||||
| chr3:136274233 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-9604T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274233 | |||||||
| chr3:136274264 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0111 |
2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.544-9573T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274264 | |||||||
| chr3:136274334 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0111 |
2 | HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.544-9503G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274334 | |||||||
| chr3:136274434 | G | C | 5 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0082 others(2): Show |
5 | HG00323.hp2 HG01346.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-9403G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274434 | |||||||
| chr3:136274592 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.544-9245A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274592 | |||||||
| chr3:136274757 | A | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.544-9080A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274757 | |||||||
| chr3:136274809 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-9028G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274809 | |||||||
| chr3:136274941 | T | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-8896T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274941 | |||||||
| chr3:136274978 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.544-8859T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274978 | |||||||
| chr3:136274985 | G | GT | 4 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0115 others(1): Show |
4 | HG01928.hp2 NA18952.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-8844dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136274985 | ||||||
| chr3:136275064 | G | T | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.544-8773G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275064 | |||||||
| chr3:136275201 | G | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
196 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.544-8636G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275201 | |||||||
| chr3:136275237 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-8600A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275237 | |||||||
| chr3:136275269 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-8568G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275269 | |||||||
| chr3:136275269 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.544-8568G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275269 | |||||||
| chr3:136275626 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0273 |
2 | HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.544-8211C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275626 | |||||||
| chr3:136275632 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.544-8205G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275632 | |||||||
| chr3:136275796 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.544-8041C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275796 | |||||||
| chr3:136275797 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
8 | HG00642.hp2 HG01175.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-8040G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275797 | |||||||
| chr3:136275821 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-8016A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275821 | |||||||
| chr3:136275863 | C | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-7974C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275863 | |||||||
| chr3:136275938 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.544-7899T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275938 | |||||||
| chr3:136275946 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-7891T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275946 | |||||||
| chr3:136275959 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(42): Show |
47 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.544-7878C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275959 | |||||||
| chr3:136275969 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0285 |
2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.544-7868G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275969 | |||||||
| chr3:136276174 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.544-7663T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276174 | |||||||
| chr3:136276185 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-7652T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276185 | |||||||
| chr3:136276199 | C | A | 7 | a0001c0001t0001g0067 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01943.hp2 HG02300.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-7638C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276199 | |||||||
| chr3:136276405 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.544-7432A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276405 | |||||||
| chr3:136276424 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0280 |
2 | HG01516.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.544-7413T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276424 | |||||||
| chr3:136276523 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-7314C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276523 | |||||||
| chr3:136276558 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.544-7279C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276558 | |||||||
| chr3:136276605 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-7232C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276605 | |||||||
| chr3:136276650 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-7187A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276650 | |||||||
| chr3:136276656 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.544-7181T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276656 | |||||||
| chr3:136276764 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0106 others(1): Show |
4 | NA18943.hp1 NA18965.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-7073C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276764 | |||||||
| chr3:136276958 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-6879C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276958 | |||||||
| chr3:136277073 | C | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-6764C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277073 | |||||||
| chr3:136277119 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.544-6718G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277119 | |||||||
| chr3:136277165 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.544-6672A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277165 | |||||||
| chr3:136277260 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0155 |
3 | HG00280.hp2 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.544-6577A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277260 | |||||||
| chr3:136277487 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.544-6350T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277487 | |||||||
| chr3:136277492 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0126 |
2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.544-6345C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277492 | |||||||
| chr3:136277555 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-6282G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277555 | |||||||
| chr3:136277560 | C | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0260 |
3 | HG02258.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.544-6277C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277560 | |||||||
| chr3:136277793 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.544-6044C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277793 | |||||||
| chr3:136278028 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(103): Show |
108 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.544-5809T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278028 | |||||||
| chr3:136278264 | C | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-5573C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278264 | |||||||
| chr3:136278384 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.544-5453C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278384 | |||||||
| chr3:136278588 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.544-5249C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278588 | |||||||
| chr3:136278669 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-5168G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278669 | |||||||
| chr3:136278754 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-5083A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278754 | |||||||
| chr3:136278844 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.544-4993C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278844 | |||||||
| chr3:136278901 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-4936T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278901 | |||||||
| chr3:136278917 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-4920T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278917 | |||||||
| chr3:136279047 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-4790A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279047 | |||||||
| chr3:136279131 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.544-4706T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279131 | |||||||
| chr3:136279136 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-4701A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279136 | |||||||
| chr3:136279263 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.544-4574A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279263 | |||||||
| chr3:136279275 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-4562A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279275 | |||||||
| chr3:136279334 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0186 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.544-4503T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279334 | |||||||
| chr3:136279348 | T | G | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-4489T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279348 | |||||||
| chr3:136279611 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
202 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.544-4226T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279611 | |||||||
| chr3:136279675 | A | T | 1 | a0001c0001t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-4162A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279675 | |||||||
| chr3:136279679 | A | T | 38 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
38 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.544-4158A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279679 | |||||||
| chr3:136279706 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.544-4131C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279706 | |||||||
| chr3:136279736 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-4101C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279736 | |||||||
| chr3:136279737 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.544-4100G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279737 | |||||||
| chr3:136279768 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-4069C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279768 | |||||||
| chr3:136279793 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.544-4044G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279793 | |||||||
| chr3:136279817 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-4020A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279817 | |||||||
| chr3:136279828 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(86): Show |
91 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.544-4009T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279828 | |||||||
| chr3:136279867 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.544-3970C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279867 | |||||||
| chr3:136279975 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.544-3862A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279975 | |||||||
| chr3:136280389 | C | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.544-3448C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280389 | |||||||
| chr3:136280588 | C | T | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.544-3249C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280588 | |||||||
| chr3:136280773 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.544-3064A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280773 | |||||||
| chr3:136280814 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0180 |
4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-3023G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280814 | |||||||
| chr3:136280933 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.544-2904T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280933 | |||||||
| chr3:136280944 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-2893G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280944 | |||||||
| chr3:136281022 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.544-2815A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281022 | |||||||
| chr3:136281249 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.544-2588T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281249 | |||||||
| chr3:136281252 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.544-2585G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281252 | |||||||
| chr3:136281305 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-2532C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281305 | |||||||
| chr3:136281485 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544-2352T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281485 | |||||||
| chr3:136281500 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-2337G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281500 | |||||||
| chr3:136281507 | A | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
17 | HG01123.hp1 HG02698.hp2 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.544-2330A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281507 | |||||||
| chr3:136281636 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-2201T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281636 | |||||||
| chr3:136281763 | C | G | 1 | a0001c0001t0001g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.544-2074C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281763 | |||||||
| chr3:136281769 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-2068T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281769 | |||||||
| chr3:136281774 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.544-2063G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281774 | |||||||
| chr3:136281817 | G | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-2020G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281817 | |||||||
| chr3:136281901 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.544-1936A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281901 | |||||||
| chr3:136281904 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.544-1933T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281904 | |||||||
| chr3:136282368 | C | G | 1 | a0003c0007t0001g0223 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.544-1469C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282368 | |||||||
| chr3:136282370 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 |
3 | HG02280.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.544-1467G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282370 | |||||||
| chr3:136282424 | T | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-1413T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282424 | |||||||
| chr3:136282520 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 |
3 | HG02280.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.544-1317G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282520 | |||||||
| chr3:136282844 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.544-993C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282844 | |||||||
| chr3:136282866 | C | T | 2 | a0001c0001t0001g0089 a0007c0004t0001g0087 |
2 | NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.544-971C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282866 | |||||||
| chr3:136282903 | A | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0001c0001t0001g0169 |
3 | HG01255.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.544-934A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282903 | |||||||
| chr3:136282945 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.544-892G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282945 | |||||||
| chr3:136283026 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.544-811A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136283026 | |||||||
| chr3:136283050 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-787G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136283050 | |||||||
| chr3:136283562 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.544-275A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136283562 | |||||||
| chr3:136283967 | T | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0199 others(21): Show |
25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.654+20T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136283967 | |||||||
| chr3:136284316 | T | TGATGTTT others(1): Show |
214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.654+369_654+370ins others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284316 | |||||||
| chr3:136284317 | T | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.654+370T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284317 | |||||||
| chr3:136284352 | A | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(44): Show |
49 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.654+405A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284352 | |||||||
| chr3:136284363 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0126 |
2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.654+416A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284363 | |||||||
| chr3:136284750 | A | C | 5 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+803A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284750 | |||||||
| chr3:136284826 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0176 others(1): Show |
4 | HG00738.hp1 HG01109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+879G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284826 | |||||||
| chr3:136284854 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+907A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284854 | |||||||
| chr3:136284871 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.654+924G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284871 | |||||||
| chr3:136284892 | G | A | 2 | a0002c0003t0001g0207 a0002c0003t0001g0211 |
2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.654+945G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284892 | |||||||
| chr3:136285088 | CA | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.654+1161delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285088 | ||||||
| chr3:136285088 | CAA | C | 37 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(34): Show |
37 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.654+1160_654+1161d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285088 | ||||||
| chr3:136285104 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.654+1157A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285104 | |||||||
| chr3:136285240 | G | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(23): Show |
28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.654+1293G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285240 | |||||||
| chr3:136285344 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.654+1397C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285344 | |||||||
| chr3:136285463 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+1516A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285463 | |||||||
| chr3:136285552 | G | GT | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG02280.hp2 HG02738.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+1617dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285552 | ||||||
| chr3:136285966 | A | ATTATAAA others(4): Show |
1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.654+2024_654+2034d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285966 | ||||||
| chr3:136286036 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.654+2089G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286036 | |||||||
| chr3:136286073 | A | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0175 others(2): Show |
5 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+2126A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286073 | |||||||
| chr3:136286083 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.654+2136C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286083 | |||||||
| chr3:136286137 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.654+2190T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286137 | |||||||
| chr3:136286784 | G | A | 8 | a0001c0001t0001g0201 a0001c0001t0001g0225 a0001c0001t0001g0226 others(5): Show |
8 | NA18943.hp2 NA18945.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+2837G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286784 | |||||||
| chr3:136286904 | G | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0050 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.654+2957G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286904 | |||||||
| chr3:136286950 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
215 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.654+3003C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286950 | |||||||
| chr3:136286962 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654+3015C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286962 | |||||||
| chr3:136286986 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.654+3039G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286986 | |||||||
| chr3:136287038 | A | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.654+3091A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287038 | |||||||
| chr3:136287043 | A | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.654+3096A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287043 | |||||||
| chr3:136287045 | A | AT | 4 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0140 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+3098_654+3099i others(3): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287045 | |||||||
| chr3:136287045 | A | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0038 others(18): Show |
22 | HG00597.hp2 HG01106.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.654+3098A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287045 | |||||||
| chr3:136287047 | A | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+3100A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287047 | |||||||
| chr3:136287047 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+3100A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287047 | |||||||
| chr3:136287048 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+3101T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287048 | |||||||
| chr3:136287060 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+3113C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287060 | |||||||
| chr3:136287186 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+3239G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287186 | |||||||
| chr3:136287389 | TAGTA | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.654+3446_654+3449d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136287389 | ||||||
| chr3:136287439 | G | GT | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(11): Show |
14 | HG00544.hp1 HG00735.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.654+3502dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136287439 | ||||||
| chr3:136287527 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+3580G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287527 | |||||||
| chr3:136287585 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.654+3638A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287585 | |||||||
| chr3:136287734 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
207 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.654+3787T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287734 | |||||||
| chr3:136287905 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.654+3958A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287905 | |||||||
| chr3:136288142 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.654+4195T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288142 | |||||||
| chr3:136288176 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.654+4229T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288176 | |||||||
| chr3:136288381 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+4434T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288381 | |||||||
| chr3:136288415 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.654+4468A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288415 | |||||||
| chr3:136288432 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0103 |
3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.654+4485G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288432 | |||||||
| chr3:136288491 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.654+4544A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288491 | |||||||
| chr3:136288576 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.654+4629C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288576 | |||||||
| chr3:136288645 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.654+4698A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288645 | |||||||
| chr3:136288646 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.654+4699T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288646 | |||||||
| chr3:136288786 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.654+4839C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288786 | |||||||
| chr3:136288789 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.654+4842G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288789 | |||||||
| chr3:136288815 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.654+4868T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288815 | |||||||
| chr3:136289115 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.655-4641C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289115 | |||||||
| chr3:136289138 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.655-4618A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289138 | |||||||
| chr3:136289138 | A | T | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655-4618A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289138 | |||||||
| chr3:136289519 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-4237A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289519 | |||||||
| chr3:136289556 | A | G | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.655-4200A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289556 | |||||||
| chr3:136289590 | A | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0001t0001g0216 others(41): Show |
45 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.655-4166A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289590 | |||||||
| chr3:136289594 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.655-4162G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289594 | |||||||
| chr3:136289789 | C | CT | 8 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG01070.hp1 HG01081.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-3958dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | ||||||
| chr3:136289789 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(3): Show |
6 | HG01243.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-3965_655-3958d others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | ||||||
| chr3:136289789 | C | CTTTTTTT others(2): Show |
40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(37): Show |
42 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.655-3966_655-3958d others(11): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | ||||||
| chr3:136289789 | C | CTTTTTTT others(3): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0045 others(5): Show |
8 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-3958_655-3957i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | ||||||
| chr3:136289789 | C | CTTTTTTT others(4): Show |
29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(26): Show |
29 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.655-3958_655-3957i others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | ||||||
| chr3:136289789 | C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 others(2): Show |
5 | HG01069.hp2 HG01346.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.655-3958_655-3957i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | ||||||
| chr3:136290004 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.655-3752G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290004 | |||||||
| chr3:136290068 | A | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3688A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290068 | |||||||
| chr3:136290102 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.655-3654A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290102 | |||||||
| chr3:136290162 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.655-3594T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290162 | |||||||
| chr3:136290250 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.655-3506G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290250 | |||||||
| chr3:136290671 | G | GTTTTTTT others(3): Show |
19 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0054 others(16): Show |
20 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.655-3077_655-3068d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | ||||||
| chr3:136290671 | G | GTTTTTTT others(4): Show |
194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.655-3078_655-3068d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | ||||||
| chr3:136290671 | G | GTTTTTTT others(5): Show |
64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
67 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.655-3079_655-3068d others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | ||||||
| chr3:136290671 | G | GTTTTTTT others(6): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0140 others(6): Show |
9 | HG00621.hp1 HG01346.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.655-3080_655-3068d others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | ||||||
| chr3:136290671 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.655-3081_655-3068d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | ||||||
| chr3:136290688 | T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0182 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.655-3068_655-3067i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290688 | |||||||
| chr3:136290688 | T | TTTTTTTT others(6): Show |
1 | a0001c0001t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-3068_655-3067i others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290688 | |||||||
| chr3:136290748 | A | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0001t0001g0202 others(42): Show |
46 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.655-3008A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290748 | |||||||
| chr3:136290757 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-2999A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290757 | |||||||
| chr3:136290842 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.655-2914C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290842 | |||||||
| chr3:136291480 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.655-2276G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291480 | |||||||
| chr3:136291539 | CCTCTGAA others(4): Show |
C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0128 a0001c0001t0001g0130 others(3): Show |
6 | HG01943.hp2 HG02300.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-2216_655-2206d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291539 | |||||||
| chr3:136291628 | T | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(25): Show |
30 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.655-2128T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291628 | |||||||
| chr3:136291774 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.655-1982G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291774 | |||||||
| chr3:136291898 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.655-1858A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291898 | |||||||
| chr3:136291908 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0002g0046 others(1): Show |
4 | HG01496.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-1848G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291908 | |||||||
| chr3:136292051 | G | A | 2 | a0002c0003t0001g0207 a0002c0003t0001g0211 |
2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.655-1705G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292051 | |||||||
| chr3:136292160 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.655-1596T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292160 | |||||||
| chr3:136292230 | T | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG01943.hp2 HG02300.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-1526T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292230 | |||||||
| chr3:136292236 | G | GT | 54 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
54 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.655-1506dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136292236 | ||||||
| chr3:136292236 | GT | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-1506delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136292236 | ||||||
| chr3:136292287 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655-1469A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292287 | |||||||
| chr3:136292395 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.655-1361A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292395 | |||||||
| chr3:136292402 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.655-1354A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292402 | |||||||
| chr3:136292535 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-1221A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292535 | |||||||
| chr3:136292564 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.655-1192C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292564 | |||||||
| chr3:136292778 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.655-978A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292778 | |||||||
| chr3:136292993 | C | A | 10 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
10 | HG00621.hp2 HG02080.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-763C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292993 | |||||||
| chr3:136293009 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-747T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293009 | |||||||
| chr3:136293379 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-377T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293379 | |||||||
| chr3:136293513 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-243A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293513 | |||||||
| chr3:136293551 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-205T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293551 | |||||||
| chr3:136293921 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.763+57C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136293921 | |||||||
| chr3:136294075 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+211C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294075 | |||||||
| chr3:136294108 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.763+244A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294108 | |||||||
| chr3:136294187 | TTTATC | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+328_763+332del others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 136294187 | ||||||
| chr3:136294254 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.763+390A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294254 | |||||||
| chr3:136294279 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.763+415A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294279 | |||||||
| chr3:136294320 | C | CT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.763+465dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 136294320 | ||||||
| chr3:136294478 | A | T | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.763+614A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294478 | |||||||
| chr3:136294702 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.763+838C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294702 | |||||||
| chr3:136294720 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.763+856C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294720 | |||||||
| chr3:136294857 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.763+993A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294857 | |||||||
| chr3:136295356 | A | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0199 others(21): Show |
25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.763+1492A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136295356 | |||||||
| chr3:136295776 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.763+1912C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136295776 | |||||||
| chr3:136295866 | G | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.763+2002G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136295866 | |||||||
| chr3:136296081 | G | A | 14 | a0001c0001t0001g0051 a0001c0001t0001g0200 a0001c0001t0001g0212 others(11): Show |
14 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.764-1871G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296081 | |||||||
| chr3:136296089 | A | G | 5 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-1863A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296089 | |||||||
| chr3:136296242 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.764-1710C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296242 | |||||||
| chr3:136296284 | C | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-1668C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296284 | |||||||
| chr3:136296291 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-1661A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296291 | |||||||
| chr3:136296432 | G | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(23): Show |
28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.764-1520G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296432 | |||||||
| chr3:136296444 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.764-1508T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296444 | |||||||
| chr3:136296581 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.764-1371A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296581 | |||||||
| chr3:136296629 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.764-1323A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296629 | |||||||
| chr3:136296931 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.764-1021C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296931 | |||||||
| chr3:136297020 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.764-932G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297020 | |||||||
| chr3:136297317 | T | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0273 |
2 | HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.764-635T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297317 | |||||||
| chr3:136297429 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.764-523C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297429 | |||||||
| chr3:136297444 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.764-508G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297444 | |||||||
| chr3:136297494 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.764-458T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297494 | |||||||
| chr3:136297516 | T | C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG00280.hp1 HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.764-436T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297516 | |||||||
| chr3:136297636 | A | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(43): Show |
48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.764-316A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297636 | |||||||
| chr3:136297817 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0176 others(1): Show |
4 | HG00738.hp1 HG01109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-135T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297817 | |||||||
| chr3:136297926 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.764-26A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297926 | |||||||
| chr3:136298144 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.884+72C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298144 | |||||||
| chr3:136298188 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG01167.hp1 HG01169.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.884+116G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298188 | |||||||
| chr3:136298313 | G | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.884+241G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298313 | |||||||
| chr3:136298326 | AT | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.884+260delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136298326 | ||||||
| chr3:136298333 | G | C | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.884+261G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298333 | |||||||
| chr3:136298353 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.884+281G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298353 | |||||||
| chr3:136298458 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+386A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298458 | |||||||
| chr3:136298754 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.884+682C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298754 | |||||||
| chr3:136299095 | T | G | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.884+1023T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299095 | |||||||
| chr3:136299098 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.884+1026C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299098 | |||||||
| chr3:136299197 | CAT | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.884+1132_884+1133d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299197 | ||||||
| chr3:136299208 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.884+1136A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299208 | |||||||
| chr3:136299235 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.884+1163C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299235 | |||||||
| chr3:136299299 | T | C | 35 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(32): Show |
35 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.884+1227T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299299 | |||||||
| chr3:136299318 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.884+1246G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299318 | |||||||
| chr3:136299438 | ATATATGC others(5): Show |
A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1370_884+1381d others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299438 | ||||||
| chr3:136299450 | GTATGCAT others(109): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.884+1472_885-1371d others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299450 | ||||||
| chr3:136299458 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1386G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299458 | |||||||
| chr3:136299460 | G | GTATGTAT others(23): Show |
2 | a0001c0001t0001g0206 a0001c0001t0001g0273 |
2 | HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.884+1393_884+1422d others(32): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299460 | ||||||
| chr3:136299462 | ATGTATAG others(69): Show |
A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(69): Show |
74 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.884+1472_885-1411d others(78): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299462 | ||||||
| chr3:136299469 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1397G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299469 | |||||||
| chr3:136299476 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1404A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299476 | |||||||
| chr3:136299478 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1406G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299478 | |||||||
| chr3:136299478 | GTGTATGT others(73): Show |
G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.884+1416_885-1463d others(82): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299478 | ||||||
| chr3:136299484 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1412G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299484 | |||||||
| chr3:136299489 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1417T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299489 | |||||||
| chr3:136299494 | GCATGTGT others(145): Show |
G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1423_885-1384d others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299494 | |||||||
| chr3:136299502 | A | ATGTATAG others(105): Show |
3 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG01167.hp1 HG01169.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.884+1436_885-1411d others(114): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299502 | ||||||
| chr3:136299510 | GTATGCAT others(13): Show |
G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0204 |
3 | HG02109.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.884+1452_884+1471d others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299510 | ||||||
| chr3:136299538 | G | GTGTA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.884+1468_884+1471d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | ||||||
| chr3:136299538 | G | GTGTATAG others(33): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0066 |
2 | HG00741.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.885-1312_885-1273d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | ||||||
| chr3:136299538 | G | GTGTATAG others(73): Show |
1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.885-1352_885-1273d others(82): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | ||||||
| chr3:136299538 | GTGTATAG others(33): Show |
G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0285 |
2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.885-1312_885-1273d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | ||||||
| chr3:136299558 | A | ATGTATGT others(31): Show |
4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.885-1470_885-1433d others(40): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299558 | ||||||
| chr3:136299578 | A | ATGTATAG others(65): Show |
1 | a0001c0001t0001g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.885-1411_885-1410i others(74): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299578 | ||||||
| chr3:136299598 | A | ATGTATGT others(105): Show |
1 | a0001c0001t0001g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.885-1411_885-1410i others(114): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299598 | ||||||
| chr3:136299598 | A | ATGTATGT others(109): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG00544.hp1 NA18954.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.885-1422_885-1307d others(118): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299598 | ||||||
| chr3:136299606 | ATATGCAT others(13): Show |
A | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.885-1406_885-1387d others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299606 | ||||||
| chr3:136299634 | GTGTA | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0278 |
3 | NA18959.hp1 NA18973.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.885-1386_885-1383d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299634 | ||||||
| chr3:136299646 | A | ATATGCAT others(13): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0221 |
2 | HG01496.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.885-1366_885-1347d others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299646 | ||||||
| chr3:136299678 | A | G | 11 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0165 others(8): Show |
11 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.885-1352A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299678 | |||||||
| chr3:136299697 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(43): Show |
48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.885-1333T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299697 | |||||||
| chr3:136299718 | A | ATGTATGT others(33): Show |
4 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0106 others(1): Show |
4 | NA18943.hp1 NA18965.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-1301_885-1262d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299718 | ||||||
| chr3:136299732 | ATGTGTAT others(17): Show |
A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1272_885-1249d others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299732 | ||||||
| chr3:136299739 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.885-1291T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299739 | |||||||
| chr3:136299756 | G | GTATGTAT others(165): Show |
1 | a0001c0001t0001g0008 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.885-1273_885-1272i others(174): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | ||||||
| chr3:136299756 | G | GTATGTAT others(9): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG00544.hp1 NA18954.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.885-1273_885-1272i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | ||||||
| chr3:136299756 | G | GTATGTAT others(29): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.885-1273_885-1272i others(38): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | ||||||
| chr3:136299756 | G | GTATGTAT others(229): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.885-1273_885-1272i others(238): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | ||||||
| chr3:136299768 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.885-1262A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299768 | |||||||
| chr3:136299782 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.885-1248A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299782 | |||||||
| chr3:136299809 | GGTATGCA others(33): Show |
G | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.885-1219_885-1180d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299809 | ||||||
| chr3:136299849 | T | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-1181T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299849 | |||||||
| chr3:136299850 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1180G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299850 | |||||||
| chr3:136299851 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-1179C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299851 | |||||||
| chr3:136299878 | G | GTGTATGT others(13): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-1144_885-1143i others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299878 | ||||||
| chr3:136299880 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.885-1150G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299880 | |||||||
| chr3:136299887 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1143C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299887 | |||||||
| chr3:136299917 | T | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0278 |
3 | NA18959.hp1 NA18973.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.885-1113T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299917 | |||||||
| chr3:136299966 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1064G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299966 | |||||||
| chr3:136300007 | CAT | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0166 |
4 | HG01884.hp2 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.885-1020_885-1019d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136300007 | ||||||
| chr3:136300008 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0285 |
2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.885-1022A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300008 | |||||||
| chr3:136300023 | C | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
7 | HG01243.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-1007C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300023 | |||||||
| chr3:136300065 | AACACATA others(19): Show |
A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-955_885-930del others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136300065 | ||||||
| chr3:136300071 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.885-959T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300071 | |||||||
| chr3:136300116 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.885-914A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300116 | |||||||
| chr3:136300152 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-878A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300152 | |||||||
| chr3:136300169 | T | TGTATAA | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(84): Show |
89 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.885-856_885-855ins others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136300169 | ||||||
| chr3:136300193 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-837A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300193 | |||||||
| chr3:136300276 | G | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.885-754G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300276 | |||||||
| chr3:136300362 | A | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.885-668A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300362 | |||||||
| chr3:136300847 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.885-183C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300847 | |||||||
| chr3:136300998 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.885-32G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300998 | |||||||
| chr3:136301265 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.966+154T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301265 | |||||||
| chr3:136301316 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+205G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301316 | |||||||
| chr3:136301400 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+289G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301400 | |||||||
| chr3:136301453 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+342T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301453 | |||||||
| chr3:136301555 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.966+444G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301555 | |||||||
| chr3:136301612 | C | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0200 a0001c0001t0001g0212 others(12): Show |
15 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.966+501C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301612 | |||||||
| chr3:136301699 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.966+588T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301699 | |||||||
| chr3:136301732 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+621A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301732 | |||||||
| chr3:136301769 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+658T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301769 | |||||||
| chr3:136301891 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+780A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301891 | |||||||
| chr3:136302103 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.966+992A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302103 | |||||||
| chr3:136302106 | A | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.966+995A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302106 | |||||||
| chr3:136302133 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.966+1022A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302133 | |||||||
| chr3:136302162 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.966+1051C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302162 | |||||||
| chr3:136302171 | CTCCTGCA others(5178): Show |
C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(103): Show |
108 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.966+1061_966+6245d others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302171 | |||||||
| chr3:136302210 | C | A | 12 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0148 others(9): Show |
12 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+1099C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302210 | |||||||
| chr3:136302238 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+1127G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302238 | |||||||
| chr3:136302354 | G | T | 1 | a0001c0001t0001g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.966+1243G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302354 | |||||||
| chr3:136302477 | T | C | 4 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+1366T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302477 | |||||||
| chr3:136302583 | C | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.966+1472C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302583 | |||||||
| chr3:136302690 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+1579A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302690 | |||||||
| chr3:136302805 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0216 |
3 | HG01070.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.966+1694C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302805 | |||||||
| chr3:136302957 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+1846G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302957 | |||||||
| chr3:136303001 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.966+1890T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303001 | |||||||
| chr3:136303459 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.966+2348C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303459 | |||||||
| chr3:136303527 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+2416T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303527 | |||||||
| chr3:136303570 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.966+2459C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303570 | |||||||
| chr3:136303571 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0155 |
3 | HG00280.hp2 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.966+2460G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303571 | |||||||
| chr3:136303603 | T | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | NA18951.hp2 NA18952.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.966+2492T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303603 | |||||||
| chr3:136303986 | T | TA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+2875_966+2876i others(3): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303986 | |||||||
| chr3:136304150 | C | CT | 6 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG01175.hp1 HG01346.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3055dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136304150 | ||||||
| chr3:136304150 | CT | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
6 | HG00544.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3055delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136304150 | ||||||
| chr3:136304194 | A | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0175 others(2): Show |
5 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+3083A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304194 | |||||||
| chr3:136304253 | C | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+3142C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304253 | |||||||
| chr3:136304371 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+3260C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304371 | |||||||
| chr3:136304383 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.966+3272T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304383 | |||||||
| chr3:136304386 | A | AT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(20): Show |
25 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.966+3278dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136304386 | ||||||
| chr3:136304390 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(83): Show |
88 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.966+3279A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304390 | |||||||
| chr3:136304403 | T | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.966+3292T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304403 | |||||||
| chr3:136304420 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0034 |
2 | HG02015.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.966+3309C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304420 | |||||||
| chr3:136304443 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.966+3332G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304443 | |||||||
| chr3:136304525 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.966+3414G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304525 | |||||||
| chr3:136304627 | T | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0200 a0001c0001t0001g0212 others(12): Show |
15 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.966+3516T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304627 | |||||||
| chr3:136304826 | T | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+3715T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304826 | |||||||
| chr3:136304848 | C | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0001t0001g0202 others(41): Show |
45 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.966+3737C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304848 | |||||||
| chr3:136304958 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.966+3847G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304958 | |||||||
| chr3:136304982 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.966+3871C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304982 | |||||||
| chr3:136304999 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.966+3888C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304999 | |||||||
| chr3:136305001 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3890A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305001 | |||||||
| chr3:136305155 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+4044C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305155 | |||||||
| chr3:136305255 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.966+4144T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305255 | |||||||
| chr3:136305379 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.966+4268A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305379 | |||||||
| chr3:136305519 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+4408C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305519 | |||||||
| chr3:136305691 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.966+4580A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305691 | |||||||
| chr3:136305746 | T | TA | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(25): Show |
30 | HG00544.hp1 HG00738.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.966+4650dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136305746 | ||||||
| chr3:136305746 | TA | T | 22 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): Show |
22 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.966+4650delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136305746 | ||||||
| chr3:136305762 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+4651G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305762 | |||||||
| chr3:136305802 | G | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+4691G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305802 | |||||||
| chr3:136305816 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.966+4705T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305816 | |||||||
| chr3:136305888 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+4777A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305888 | |||||||
| chr3:136306214 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+5103G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136306214 | |||||||
| chr3:136306477 | A | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(23): Show |
28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.966+5366A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136306477 | |||||||
| chr3:136307090 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0270 a0001c0001t0001g0275 |
3 | HG02976.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.966+5979G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307090 | |||||||
| chr3:136307350 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.966+6239G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307350 | |||||||
| chr3:136307357 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(103): Show |
108 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.966+6246G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307357 | |||||||
| chr3:136307438 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+6327T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307438 | |||||||
| chr3:136307439 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+6328C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307439 | |||||||
| chr3:136307442 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+6331C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307442 | |||||||
| chr3:136307642 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+6531G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307642 | |||||||
| chr3:136307688 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0103 |
3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.966+6577A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307688 | |||||||
| chr3:136307747 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+6636G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307747 | |||||||
| chr3:136307889 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.966+6778C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307889 | |||||||
| chr3:136307977 | A | AAAT | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(33): Show |
38 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.966+6889_966+6891d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136307977 | ||||||
| chr3:136307977 | A | AAATAATA others(2): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+6883_966+6891d others(11): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136307977 | ||||||
| chr3:136307977 | AAATAAT | A | 30 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(27): Show |
30 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.966+6886_966+6891d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136307977 | ||||||
| chr3:136308025 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+6914C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308025 | |||||||
| chr3:136308191 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0002g0046 others(1): Show |
4 | HG01496.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+7080T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308191 | |||||||
| chr3:136308234 | C | CT | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.966+7140dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136308234 | ||||||
| chr3:136308234 | C | CTT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0099 a0001c0001t0001g0122 others(3): Show |
6 | HG02074.hp1 HG06807.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+7139_966+7140d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136308234 | ||||||
| chr3:136308303 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.966+7192A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308303 | |||||||
| chr3:136308493 | G | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+7382G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308493 | |||||||
| chr3:136308707 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.966+7596A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308707 | |||||||
| chr3:136308798 | G | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0001t0001g0216 others(40): Show |
44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.966+7687G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308798 | |||||||
| chr3:136309055 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-7886G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309055 | |||||||
| chr3:136309092 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.967-7849G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309092 | |||||||
| chr3:136309151 | T | C | 1 | a0001c0001t0001g0010 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.967-7790T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309151 | |||||||
| chr3:136309166 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.967-7775G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309166 | |||||||
| chr3:136309212 | C | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-7729C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309212 | |||||||
| chr3:136309262 | C | CA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0065 others(4): Show |
7 | HG02280.hp2 HG02300.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-7661dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136309262 | ||||||
| chr3:136309262 | CA | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
10 | HG00544.hp1 HG01169.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.967-7661delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136309262 | ||||||
| chr3:136309486 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-7455T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309486 | |||||||
| chr3:136309659 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01243.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-7282G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309659 | |||||||
| chr3:136309801 | CA | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(5): Show |
9 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.967-7126delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136309801 | ||||||
| chr3:136309998 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.967-6943A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309998 | |||||||
| chr3:136310145 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(99): Show |
104 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.967-6796C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310145 | |||||||
| chr3:136310193 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-6748G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310193 | |||||||
| chr3:136310295 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.967-6646G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310295 | |||||||
| chr3:136310303 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.967-6638C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310303 | |||||||
| chr3:136310318 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-6623G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310318 | |||||||
| chr3:136310351 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-6590G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310351 | |||||||
| chr3:136310397 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0242 a0001c0001t0001g0257 |
3 | NA18952.hp2 NA19082.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.967-6544C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310397 | |||||||
| chr3:136310416 | G | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0037 others(28): Show |
32 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.967-6525G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310416 | |||||||
| chr3:136310422 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.967-6519C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310422 | |||||||
| chr3:136310515 | C | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0271 |
2 | HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.967-6426C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310515 | |||||||
| chr3:136310618 | TAGAAAGT others(17): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.967-6321_967-6298d others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136310618 | ||||||
| chr3:136310647 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.967-6294T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310647 | |||||||
| chr3:136310724 | T | G | 5 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.967-6217T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310724 | |||||||
| chr3:136310769 | C | G | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00609.hp1 HG01884.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-6172C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310769 | |||||||
| chr3:136310881 | T | C | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.967-6060T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310881 | |||||||
| chr3:136310900 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.967-6041G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310900 | |||||||
| chr3:136311074 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.967-5867C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311074 | |||||||
| chr3:136311205 | G | T | 1 | a0001c0001t0001g0015 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.967-5736G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311205 | |||||||
| chr3:136311348 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.967-5593T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311348 | |||||||
| chr3:136311443 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-5498C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311443 | |||||||
| chr3:136311450 | A | G | 1 | a0006c0006t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.967-5491A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311450 | |||||||
| chr3:136311454 | A | G | 1 | a0005c0008t0001g0231 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.967-5487A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311454 | |||||||
| chr3:136311510 | A | AT | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
10 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-5420dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136311510 | ||||||
| chr3:136311559 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-5382C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311559 | |||||||
| chr3:136311604 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG00738.hp2 HG01106.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-5337T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311604 | |||||||
| chr3:136311918 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.967-5023C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311918 | |||||||
| chr3:136312175 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-4766G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312175 | |||||||
| chr3:136312316 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.967-4625C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312316 | |||||||
| chr3:136312516 | G | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.967-4425G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312516 | |||||||
| chr3:136312636 | T | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0175 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-4305T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312636 | |||||||
| chr3:136312851 | G | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0289 |
2 | NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.967-4090G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312851 | |||||||
| chr3:136312939 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-4002C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312939 | |||||||
| chr3:136313082 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.967-3859C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313082 | |||||||
| chr3:136313207 | G | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00280.hp2 HG01081.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-3734G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313207 | |||||||
| chr3:136313253 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-3688G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313253 | |||||||
| chr3:136313356 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-3585A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313356 | |||||||
| chr3:136313472 | CA | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-3467delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136313472 | ||||||
| chr3:136313483 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-3458G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313483 | |||||||
| chr3:136313644 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.967-3297A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313644 | |||||||
| chr3:136313820 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0050 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.967-3121T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313820 | |||||||
| chr3:136314032 | T | TCA | 36 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(33): Show |
36 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.967-2894_967-2893d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136314032 | ||||||
| chr3:136314032 | T | TCACA | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-2896_967-2893d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136314032 | ||||||
| chr3:136314186 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.967-2755A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136314186 | |||||||
| chr3:136314439 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.967-2502G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136314439 | |||||||
| chr3:136314483 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.967-2458T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136314483 | |||||||
| chr3:136314672 | AAACAAAA others(4): Show |
A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-2266_967-2256d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136314672 | ||||||
| chr3:136315109 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1832T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315109 | |||||||
| chr3:136315110 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1831A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315110 | |||||||
| chr3:136315161 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1780A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315161 | |||||||
| chr3:136315264 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.967-1677G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315264 | |||||||
| chr3:136315274 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0123 others(2): Show |
6 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1667A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315274 | |||||||
| chr3:136315313 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.967-1628G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315313 | |||||||
| chr3:136315331 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.967-1610C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315331 | |||||||
| chr3:136315365 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.967-1576C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315365 | |||||||
| chr3:136315458 | C | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG00280.hp1 HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.967-1483C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315458 | |||||||
| chr3:136315613 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.967-1328G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315613 | |||||||
| chr3:136315648 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.967-1293T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315648 | |||||||
| chr3:136315661 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(43): Show |
48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.967-1280T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315661 | |||||||
| chr3:136315678 | A | AT | 9 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00099.hp1 HG00733.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.967-1251dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136315678 | ||||||
| chr3:136315879 | C | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0121 a0001c0001t0001g0125 others(1): Show |
4 | HG00423.hp2 NA18963.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-1062C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315879 | |||||||
| chr3:136315899 | G | C | 8 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0150 others(5): Show |
8 | HG00280.hp2 HG01081.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-1042G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315899 | |||||||
| chr3:136315911 | T | TTA | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(42): Show |
47 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.967-1019_967-1018d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136315911 | ||||||
| chr3:136315925 | AAGAG | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1011_967-1008d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136315925 | ||||||
| chr3:136315969 | C | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0103 |
3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.967-972C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315969 | |||||||
| chr3:136316006 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.967-935G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316006 | |||||||
| chr3:136316181 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-760C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316181 | |||||||
| chr3:136316184 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-757C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316184 | |||||||
| chr3:136316226 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.967-715A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316226 | |||||||
| chr3:136316227 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.967-714G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316227 | |||||||
| chr3:136316227 | G | GA | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-701dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136316227 | ||||||
| chr3:136316277 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(43): Show |
48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.967-664G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316277 | |||||||
| chr3:136316363 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-578T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316363 | |||||||
| chr3:136316375 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.967-566G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316375 | |||||||
| chr3:136316461 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.967-480C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316461 | |||||||
| chr3:136316489 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-452C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316489 | |||||||
| chr3:136316895 | A | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(78): Show |
83 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.967-46A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316895 | |||||||
| chr3:136316899 | G | C | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.967-42G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316899 | |||||||
| chr3:136317212 | A | AT | 59 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0023 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1090+178dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | A | ATT | 18 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(15): Show |
18 | HG00423.hp1 HG00738.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1090+177_1090+178d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | A | ATTT | 14 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0125 others(11): Show |
15 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1090+176_1090+178d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | A | ATTTT | 56 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0054 others(53): Show |
56 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1090+175_1090+178d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | A | ATTTTT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0049 others(30): Show |
34 | HG00609.hp1 HG00621.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1090+174_1090+178d others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | A | ATTTTTT | 6 | a0001c0001t0001g0070 a0001c0001t0001g0085 a0001c0001t0001g0092 others(3): Show |
6 | HG00423.hp2 HG01123.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+173_1090+178d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | AT | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1090+178delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | ATTTTTTT | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(24): Show |
27 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.1090+172_1090+178d others(9): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317212 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1090+169_1090+178d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | ||||||
| chr3:136317265 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+201A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317265 | |||||||
| chr3:136317347 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1090+283G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317347 | |||||||
| chr3:136317358 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+294A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317358 | |||||||
| chr3:136317384 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
202 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1090+320A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317384 | |||||||
| chr3:136317387 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1090+323A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317387 | |||||||
| chr3:136317494 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 |
3 | HG02280.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1090+430G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317494 | |||||||
| chr3:136317846 | G | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | NA18951.hp2 NA18952.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1090+782G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317846 | |||||||
| chr3:136318144 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1090+1080T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318144 | |||||||
| chr3:136318215 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1090+1151C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318215 | |||||||
| chr3:136318226 | T | TC | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+1164dupC | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136318226 | ||||||
| chr3:136318328 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1090+1264T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318328 | |||||||
| chr3:136318385 | A | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(109): Show |
114 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1090+1321A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318385 | |||||||
| chr3:136318386 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0105 |
3 | HG01123.hp1 NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1090+1322A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318386 | |||||||
| chr3:136318659 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1090+1595C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318659 | |||||||
| chr3:136318696 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+1632C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318696 | |||||||
| chr3:136318768 | ATAT | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0123 others(2): Show |
6 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+1708_1090+171 others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136318768 | ||||||
| chr3:136318865 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(108): Show |
113 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1090+1801G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318865 | |||||||
| chr3:136318882 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0133 |
2 | NA19058.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1090+1818A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318882 | |||||||
| chr3:136318900 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG00099.hp2 HG01168.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090+1836C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318900 | |||||||
| chr3:136318925 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+1861G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318925 | |||||||
| chr3:136319097 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1090+2033G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319097 | |||||||
| chr3:136319125 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0050 |
3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1090+2061A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319125 | |||||||
| chr3:136319160 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1090+2096A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319160 | |||||||
| chr3:136319209 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1090+2145C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319209 | |||||||
| chr3:136319356 | C | T | 9 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0150 others(6): Show |
9 | HG00280.hp2 HG01081.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1090+2292C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319356 | |||||||
| chr3:136319386 | A | AT | 29 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(26): Show |
31 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1090+2338dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136319386 | ||||||
| chr3:136319386 | A | ATT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG01123.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1090+2337_1090+233 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136319386 | ||||||
| chr3:136319453 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0271 |
2 | HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1090+2389A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319453 | |||||||
| chr3:136319460 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+2396G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319460 | |||||||
| chr3:136319483 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1090+2419G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319483 | |||||||
| chr3:136319522 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1090+2458C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319522 | |||||||
| chr3:136319564 | ATTTTTGT others(28): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1090+2501_1090+253 others(39): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319564 | |||||||
| chr3:136319579 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1090+2515G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319579 | |||||||
| chr3:136319600 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1090+2536G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319600 | |||||||
| chr3:136319617 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+2553C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319617 | |||||||
| chr3:136319732 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1090+2668G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319732 | |||||||
| chr3:136319767 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1090+2703G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319767 | |||||||
| chr3:136319834 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1090+2770G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319834 | |||||||
| chr3:136319895 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1090+2831T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319895 | |||||||
| chr3:136319941 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+2877G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319941 | |||||||
| chr3:136320146 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1090+3082A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320146 | |||||||
| chr3:136320200 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1090+3136A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320200 | |||||||
| chr3:136320426 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1090+3362C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320426 | |||||||
| chr3:136320578 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+3514G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320578 | |||||||
| chr3:136320648 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+3584T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320648 | |||||||
| chr3:136320798 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(25): Show |
30 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1090+3734C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320798 | |||||||
| chr3:136320801 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(25): Show |
30 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1090+3737A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320801 | |||||||
| chr3:136320971 | C | A | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1090+3907C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320971 | |||||||
| chr3:136321146 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1090+4082G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321146 | |||||||
| chr3:136321249 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1090+4185A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321249 | |||||||
| chr3:136321546 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1090+4482G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321546 | |||||||
| chr3:136321601 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG02896.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1090+4537C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321601 | |||||||
| chr3:136321728 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
11 | HG00544.hp1 HG01243.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1090+4664C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321728 | |||||||
| chr3:136321740 | G | C | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1090+4676G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321740 | |||||||
| chr3:136321883 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1090+4819G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321883 | |||||||
| chr3:136321922 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0050 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1090+4858T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321922 | |||||||
| chr3:136321929 | A | T | 5 | a0001c0001t0001g0201 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | NA18953.hp2 NA18964.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090+4865A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321929 | |||||||
| chr3:136321957 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0059 others(4): Show |
7 | HG01123.hp1 NA18948.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-4846A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321957 | |||||||
| chr3:136322215 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0275 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1091-4588G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322215 | |||||||
| chr3:136322681 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1091-4122C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322681 | |||||||
| chr3:136322726 | G | T | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG02135.hp2 NA18747.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-4077G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322726 | |||||||
| chr3:136322741 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1091-4062C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322741 | |||||||
| chr3:136322914 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-3889A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322914 | |||||||
| chr3:136322998 | GT | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1091-3787delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136322998 | ||||||
| chr3:136322998 | GTT | G | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
39 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.1091-3788_1091-378 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136322998 | ||||||
| chr3:136323005 | T | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(2): Show |
5 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1091-3798T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323005 | |||||||
| chr3:136323006 | T | G | 1 | a0001c0001t0001g0010 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1091-3797T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323006 | |||||||
| chr3:136323079 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1091-3724T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323079 | |||||||
| chr3:136323126 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1091-3677G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323126 | |||||||
| chr3:136323313 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0166 |
4 | HG01884.hp2 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-3490A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323313 | |||||||
| chr3:136323322 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(77): Show |
82 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.1091-3481T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323322 | |||||||
| chr3:136323543 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091-3260A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323543 | |||||||
| chr3:136323590 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-3213C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323590 | |||||||
| chr3:136323641 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1091-3162C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323641 | |||||||
| chr3:136323714 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1091-3089G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323714 | |||||||
| chr3:136323774 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091-3029A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323774 | |||||||
| chr3:136323807 | C | CA | 40 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(37): Show |
41 | HG00621.hp1 HG00642.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1091-2980dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323807 | ||||||
| chr3:136323807 | C | CAA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG00544.hp1 HG01175.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1091-2981_1091-298 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323807 | ||||||
| chr3:136323807 | CA | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0196 others(3): Show |
6 | HG01106.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1091-2980delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323807 | ||||||
| chr3:136323877 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1091-2926C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323877 | |||||||
| chr3:136323899 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0170 |
2 | HG01255.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1091-2904T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323899 | |||||||
| chr3:136323957 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0035 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1091-2846G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323957 | |||||||
| chr3:136323992 | G | GT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1091-2797dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323992 | ||||||
| chr3:136324064 | C | CTG | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091-2738_1091-273 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136324064 | ||||||
| chr3:136324505 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1091-2298C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324505 | |||||||
| chr3:136324506 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1091-2297G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324506 | |||||||
| chr3:136324550 | T | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(48): Show |
53 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1091-2253T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324550 | |||||||
| chr3:136324663 | G | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1091-2140G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324663 | |||||||
| chr3:136324756 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0119 others(23): Show |
28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.1091-2047G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324756 | |||||||
| chr3:136324954 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1091-1849A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324954 | |||||||
| chr3:136324986 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1091-1817A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324986 | |||||||
| chr3:136325041 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1091-1762C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325041 | |||||||
| chr3:136325046 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1091-1757C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325046 | |||||||
| chr3:136325097 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1091-1706C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325097 | |||||||
| chr3:136325292 | G | GGGAC | 3 | a0001c0001t0001g0051 a0001c0001t0001g0212 a0001c0001t0001g0215 |
3 | NA18946.hp2 NA19060.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1091-1510_1091-150 others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136325292 | ||||||
| chr3:136325390 | TCTCA | T | 21 | a0001c0001t0001g0037 a0001c0001t0001g0142 a0001c0001t0001g0143 others(18): Show |
21 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1091-1409_1091-140 others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136325390 | ||||||
| chr3:136325513 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1091-1290C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325513 | |||||||
| chr3:136325609 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0233 |
3 | HG02080.hp1 NA18986.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1091-1194G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325609 | |||||||
| chr3:136325651 | C | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1091-1152C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325651 | |||||||
| chr3:136325801 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1091-1002C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325801 | |||||||
| chr3:136325844 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-959T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325844 | |||||||
| chr3:136325963 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-840G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325963 | |||||||
| chr3:136326087 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-716C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326087 | |||||||
| chr3:136326209 | TG | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-592delG | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136326209 | ||||||
| chr3:136326273 | C | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091-530C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326273 | |||||||
| chr3:136326371 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1091-432G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326371 | |||||||
| chr3:136326382 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-421G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326382 | |||||||
| chr3:136326431 | G | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091-372G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326431 | |||||||
| chr3:136326787 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1091-16A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326787 | |||||||
| chr3:136327909 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1398+177T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136327909 | |||||||
| chr3:136327934 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0256 |
2 | NA18951.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1398+202C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136327934 | |||||||
| chr3:136327970 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0263 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1398+238C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136327970 | |||||||
| chr3:136328066 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1398+334T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328066 | |||||||
| chr3:136328339 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1399-419C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328339 | |||||||
| chr3:136328347 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(108): Show |
113 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1399-411A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328347 | |||||||
| chr3:136328458 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-300A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328458 | |||||||
| chr3:136328535 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1399-223T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328535 | |||||||
| chr3:136328540 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1399-218G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328540 | |||||||
| chr3:136328546 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1399-212G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328546 | |||||||
| chr3:136329074 | T | TAACACCA others(32): Show |
1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+217_1498+218i others(41): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329074 | |||||||
| chr3:136329075 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+218T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329075 | |||||||
| chr3:136329078 | ATTTCTAG others(28): Show |
A | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+222_1498+256d others(37): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329078 | |||||||
| chr3:136329089 | T | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1498+232T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329089 | |||||||
| chr3:136329097 | G | T | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1498+240G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329097 | |||||||
| chr3:136329135 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
207 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1498+278A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329135 | |||||||
| chr3:136329157 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+300T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329157 | |||||||
| chr3:136329166 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+309G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329166 | |||||||
| chr3:136329168 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+311T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329168 | |||||||
| chr3:136329169 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+312T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329169 | |||||||
| chr3:136329170 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+313A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329170 | |||||||
| chr3:136329333 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1498+476C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329333 | |||||||
| chr3:136329358 | A | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498+501A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329358 | |||||||
| chr3:136329676 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1499-229C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329676 | |||||||
| chr3:136329860 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1499-45A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329860 | |||||||
| chr3:136329885 | C | T | 2 | a0001c0001t0001g0089 a0007c0004t0001g0087 |
2 | NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1499-20C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329885 |