Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5110 |
| ensemblid | ENSG00000120265.21 |
| hgncid | 8728 |
| symbol | PCMT1 |
| name | protein-L-isoaspartate (D-aspartate) O-methyltransferase |
| refseq_nuc | NM_001360452.2 |
| refseq_prot | NP_001347381.1 |
| ensembl_nuc | ENST00000464889.7 |
| ensembl_prot | ENSP00000420813.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 149749741 |
| end | 149811419 |
| strand | + |
| ver | v1.2 |
| region | chr6:149749741-149811419 |
| region5000 | chr6:149744741-149816419 |
| regionname0 | PCMT1_chr6_149749741_149811419 |
| regionname5000 | PCMT1_chr6_149744741_149816419 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 227 | 239 | 84 | 36 | 89 | 7 | 22 | 67 | PCMT1_chr6_149744741_149816419 | PCMT1 | MAWKS others(222): Show |
chr6 | 149744741 | 149816419 |
| a0002 | 1/0 | 227 | 95 | 8 | 24 | 39 | 9 | 14 | 35 | PCMT1_chr6_149744741_149816419 | PCMT1 | MAWKS others(222): Show |
chr6 | 149744741 | 149816419 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 681 | 239 | 84 | 36 | 89 | 7 | 22 | PCMT1_chr6_149744741_149816419 | PCMT1 | ATGGC others(676): Show |
chr6 | 149744741 | 149816419 | ||
| a0002c0002 | 1/0 | 681 | 94 | 8 | 24 | 38 | 9 | 14 | PCMT1_chr6_149744741_149816419 | PCMT1 | ATGGC others(676): Show |
chr6 | 149744741 | 149816419 | ||
| a0002c0003 | 0/0 | 681 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | ATGGC others(676): Show |
chr6 | 149744741 | 149816419 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1686 | 233 | 81 | 35 | 88 | 7 | 21 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0001c0001t0004 | 0/0 | 1686 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0001c0001t0005 | 0/0 | 1686 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0001c0001t0006 | 0/0 | 1686 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0001c0001t0007 | 0/0 | 1686 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0001c0001t0008 | 0/0 | 1686 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0001c0001t0009 | 0/0 | 1686 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0002c0002t0002 | 1/0 | 1686 | 92 | 8 | 24 | 38 | 9 | 12 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0002c0002t0003 | 0/0 | 1686 | 2 | 0 | 0 | 0 | 0 | 2 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| a0002c0003t0002 | 0/0 | 1686 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | GCAGT others(1681): Show |
chr6 | 149744741 | 149816419 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0008g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0001c0001t0009g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| a0002c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0085 | EUR | GBR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0069 | EUR | FIN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0047 | EUR | FIN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0025 | EUR | FIN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0145 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0088 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0068 | AMR | PUR | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0038 | EUR | IBS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0035 | EUR | IBS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0039 | EUR | IBS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0289 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02080 | hp1 | a0002 | c0003 | t0002 | g0020 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CDX | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0040 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0084 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0037 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0029 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0042 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0049 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0104 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0080 | SAS | PJL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03942 | hp1 | a0002 | c0002 | t0003 | g0030 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | STU | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19082 | hp1 | a0001 | c0001 | t0008 | g0294 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0332 | AFR | ASW | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ASW | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0066 | EUR | TSI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | USA | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | USA | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0171 | REF | REF | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0041 | REF | REF | PCMT1_chr6_149744741_149816419 | PCMT1 | chr6 | 149744741 | 149816419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149793609 | G | A | 1 | a0001 | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
missense_variant | MODERATE | c.358G>A | p.Val120Ile | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/8 | 519/1686 | 358/684 | 120/227 | chr6 | 149793609 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149802325 | G | A | 1 | a0002c0003 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.630G>A | p.Gly210Gly | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/8 | 791/1686 | 630/684 | 210/227 | chr6 | 149802325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149749772 | C | T | 1 | a0001c0001t0009 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-130C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/8 | 130 | chr6 | 149749772 | ||||||
| chr6:149749795 | C | T | 1 | a0001c0001t0008 | 1 | NA19082.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/8 | 107 | chr6 | 149749795 | ||||||
| chr6:149749880 | C | T | 1 | a0001c0001t0007 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/8 | 22 | chr6 | 149749880 | ||||||
| chr6:149810956 | A | G | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(4): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*378A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 8/8 | 8577 | chr6 | 149810956 | ||||||
| chr6:149811014 | C | T | 1 | a0001c0001t0006 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 8/8 | 8635 | chr6 | 149811014 | ||||||
| chr6:149811044 | G | T | 1 | a0002c0002t0003 | 2 | HG02698.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*466G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 8/8 | 8665 | chr6 | 149811044 | ||||||
| chr6:149811152 | C | T | 1 | a0001c0001t0005 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*574C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 8/8 | 8773 | chr6 | 149811152 | ||||||
| chr6:149811183 | A | T | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(4): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*605A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 8/8 | 8804 | chr6 | 149811183 | ||||||
| chr6:149811210 | C | T | 1 | a0001c0001t0004 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*632C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 8/8 | 8831 | chr6 | 149811210 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149750053 | C | T | 1 | a0002c0002t0002g0332 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.55+97C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750053 | |||||||
| chr6:149750248 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG00423.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.55+292G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750248 | |||||||
| chr6:149750280 | C | CCGGCTT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
13 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+325_55+330dupCG others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149750280 | ||||||
| chr6:149750397 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.55+441C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750397 | |||||||
| chr6:149750551 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55+595T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750551 | |||||||
| chr6:149750573 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.55+617G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750573 | |||||||
| chr6:149750599 | G | C | 1 | a0002c0003t0002g0020 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.55+643G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750599 | |||||||
| chr6:149750711 | GTGGAGTT | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 |
3 | HG02080.hp2 HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.55+757_55+763delGG others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149750711 | ||||||
| chr6:149750818 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55+862A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750818 | |||||||
| chr6:149750892 | A | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+936A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149750892 | |||||||
| chr6:149751039 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.55+1083G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751039 | |||||||
| chr6:149751060 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+1104T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751060 | |||||||
| chr6:149751096 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55+1140T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751096 | |||||||
| chr6:149751296 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.55+1340A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751296 | |||||||
| chr6:149751327 | A | T | 1 | a0001c0001t0001g0329 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.55+1371A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751327 | |||||||
| chr6:149751328 | A | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
192 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.55+1372A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751328 | |||||||
| chr6:149751359 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.55+1403C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751359 | |||||||
| chr6:149751476 | C | CT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
37 | HG00642.hp1 HG01109.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.55+1543dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149751476 | ||||||
| chr6:149751476 | C | CTT | 29 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(26): Show |
29 | HG00099.hp1 HG00733.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.55+1542_55+1543dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149751476 | ||||||
| chr6:149751476 | CT | C | 10 | a0001c0001t0001g0155 a0001c0001t0001g0199 a0001c0001t0001g0200 others(7): Show |
10 | HG00558.hp1 HG02896.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.55+1543delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149751476 | ||||||
| chr6:149751476 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG00741.hp1 HG02056.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+1534_55+1543del others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149751476 | ||||||
| chr6:149751476 | CTTTTTTT others(4): Show |
C | 37 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.55+1533_55+1543del others(11): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149751476 | ||||||
| chr6:149751542 | C | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
191 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.55+1586C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751542 | |||||||
| chr6:149751562 | A | C | 3 | a0002c0002t0002g0101 a0002c0002t0002g0112 a0002c0002t0002g0113 |
3 | HG01175.hp1 HG01261.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.55+1606A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751562 | |||||||
| chr6:149751658 | T | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+1702T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751658 | |||||||
| chr6:149751684 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+1728G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751684 | |||||||
| chr6:149751770 | G | C | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55+1814G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751770 | |||||||
| chr6:149751847 | A | T | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55+1891A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751847 | |||||||
| chr6:149751881 | A | AT | 12 | a0002c0002t0002g0089 a0002c0002t0002g0090 a0002c0002t0002g0091 others(9): Show |
12 | HG01358.hp1 HG02040.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.55+1937dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149751881 | ||||||
| chr6:149751976 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.55+2020G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751976 | |||||||
| chr6:149751977 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+2021A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149751977 | |||||||
| chr6:149752036 | G | GT | 22 | a0001c0001t0001g0018 a0001c0001t0001g0128 a0001c0001t0001g0153 others(19): Show |
22 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.55+2096dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149752036 | ||||||
| chr6:149752036 | G | GTT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
14 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+2095_55+2096dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149752036 | ||||||
| chr6:149752036 | G | GTTT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0220 others(3): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+2094_55+2096dup others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149752036 | ||||||
| chr6:149752036 | G | GTTTT | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(112): Show |
115 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.55+2093_55+2096dup others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149752036 | ||||||
| chr6:149752036 | G | GTTTTT | 40 | a0001c0001t0001g0019 a0001c0001t0001g0170 a0001c0001t0001g0172 others(37): Show |
40 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.55+2092_55+2096dup others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149752036 | ||||||
| chr6:149752281 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.55+2325T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149752281 | |||||||
| chr6:149752284 | G | GCCTCCTG others(5): Show |
1 | a0001c0001t0001g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.55+2329_55+2340dup others(12): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149752284 | ||||||
| chr6:149752399 | A | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
183 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.55+2443A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149752399 | |||||||
| chr6:149752684 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55+2728A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149752684 | |||||||
| chr6:149752755 | A | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+2799A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149752755 | |||||||
| chr6:149752814 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.55+2858T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149752814 | |||||||
| chr6:149753054 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.55+3098A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149753054 | |||||||
| chr6:149753238 | T | A | 1 | a0001c0001t0001g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.55+3282T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149753238 | |||||||
| chr6:149753298 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+3342C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149753298 | |||||||
| chr6:149753337 | G | GT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0218 a0001c0001t0001g0309 others(5): Show |
8 | HG03195.hp2 HG03688.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+3393dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149753337 | ||||||
| chr6:149753364 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+3408C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149753364 | |||||||
| chr6:149753369 | AT | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+3415delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149753369 | ||||||
| chr6:149753402 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55+3446A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149753402 | |||||||
| chr6:149753809 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.55+3853T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149753809 | |||||||
| chr6:149753911 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+3955T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149753911 | |||||||
| chr6:149754104 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55+4148G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754104 | |||||||
| chr6:149754137 | T | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.55+4181T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754137 | |||||||
| chr6:149754143 | G | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+4187G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754143 | |||||||
| chr6:149754161 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.55+4205A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754161 | |||||||
| chr6:149754182 | A | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0326 |
2 | NA18985.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.55+4226A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754182 | |||||||
| chr6:149754280 | G | T | 1 | a0002c0002t0002g0079 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.55+4324G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754280 | |||||||
| chr6:149754363 | C | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+4407C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754363 | |||||||
| chr6:149754366 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55+4410G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754366 | |||||||
| chr6:149754432 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.55+4476G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754432 | |||||||
| chr6:149754908 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.55+4952G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149754908 | |||||||
| chr6:149755084 | A | C | 1 | a0002c0002t0002g0111 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.55+5128A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755084 | |||||||
| chr6:149755099 | A | AAGGGAC | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+5144_55+5145ins others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149755099 | ||||||
| chr6:149755128 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.55+5172G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755128 | |||||||
| chr6:149755189 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55+5233T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755189 | |||||||
| chr6:149755268 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55+5312A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755268 | |||||||
| chr6:149755448 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.55+5492A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755448 | |||||||
| chr6:149755463 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.55+5507A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755463 | |||||||
| chr6:149755464 | T | G | 1 | a0001c0001t0001g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.55+5508T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755464 | |||||||
| chr6:149755688 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+5732A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755688 | |||||||
| chr6:149755716 | G | T | 1 | a0002c0002t0002g0078 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.55+5760G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755716 | |||||||
| chr6:149755822 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55+5866T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149755822 | |||||||
| chr6:149756136 | G | T | 6 | a0002c0002t0002g0073 a0002c0002t0002g0074 a0002c0002t0002g0075 others(3): Show |
6 | NA18955.hp1 NA18984.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+6180G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756136 | |||||||
| chr6:149756283 | T | TTTCTAA | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.55+6332_55+6333ins others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756283 | ||||||
| chr6:149756353 | C | CT | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
191 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.55+6410dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756353 | ||||||
| chr6:149756473 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.55+6517C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756473 | |||||||
| chr6:149756512 | C | CT | 29 | a0002c0002t0002g0054 a0002c0002t0002g0055 a0002c0002t0002g0056 others(26): Show |
29 | HG00733.hp2 HG01099.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.55+6588dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756512 | C | CTT | 10 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0002g0070 others(7): Show |
10 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.55+6587_55+6588dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756512 | CT | C | 16 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0128 others(13): Show |
16 | HG00099.hp1 HG01069.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.55+6588delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756512 | CTT | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0015 others(37): Show |
41 | HG00733.hp1 HG01192.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.55+6587_55+6588del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756512 | CTTT | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
38 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.55+6586_55+6588del others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756512 | CTTTT | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0154 others(133): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.55+6585_55+6588del others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756512 | CTTTTT | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+6584_55+6588del others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756512 | CTTTTTTT others(3): Show |
C | 4 | a0002c0002t0002g0024 a0002c0002t0002g0025 a0002c0002t0002g0026 others(1): Show |
4 | HG00323.hp2 HG01361.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+6579_55+6588del others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149756512 | ||||||
| chr6:149756514 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0002c0002t0002g0084 |
3 | HG02572.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.55+6558T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756514 | |||||||
| chr6:149756515 | T | A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0128 others(10): Show |
13 | HG00099.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+6559T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756515 | |||||||
| chr6:149756516 | T | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0015 others(37): Show |
41 | HG00733.hp1 HG01192.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.55+6560T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756516 | |||||||
| chr6:149756517 | T | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
38 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.55+6561T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756517 | |||||||
| chr6:149756518 | T | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0154 others(133): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.55+6562T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756518 | |||||||
| chr6:149756519 | T | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+6563T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756519 | |||||||
| chr6:149756656 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.55+6700C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756656 | |||||||
| chr6:149756836 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55+6880A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756836 | |||||||
| chr6:149756894 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55+6938C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756894 | |||||||
| chr6:149756953 | C | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+6997C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149756953 | |||||||
| chr6:149757017 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA19082.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.55+7061T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149757017 | |||||||
| chr6:149757379 | C | T | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55+7423C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149757379 | |||||||
| chr6:149757657 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.55+7701C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149757657 | |||||||
| chr6:149757730 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55+7774A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149757730 | |||||||
| chr6:149757841 | T | C | 2 | a0002c0002t0003g0029 a0002c0002t0003g0030 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.55+7885T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149757841 | |||||||
| chr6:149757992 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18969.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.55+8036C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149757992 | |||||||
| chr6:149758093 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+8137A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758093 | |||||||
| chr6:149758185 | A | ATT | 16 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(13): Show |
16 | HG00423.hp1 HG00642.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.55+8238_55+8239dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758185 | ||||||
| chr6:149758192 | T | TTTTTTC | 172 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(169): Show |
172 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.55+8239_55+8240ins others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758192 | ||||||
| chr6:149758208 | C | CT | 7 | a0001c0001t0001g0128 a0001c0001t0001g0312 a0001c0001t0008g0294 others(4): Show |
7 | HG02055.hp1 HG02080.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+8270dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTCTTT others(14): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0194 a0001c0001t0001g0212 |
3 | HG00642.hp2 HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.55+8255_55+8256ins others(21): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTCTTT others(15): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG02109.hp2 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+8255_55+8256ins others(22): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTCTTT others(16): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02572.hp1 HG03130.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+8255_55+8256ins others(23): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTCTTT others(17): Show |
1 | a0001c0001t0001g0305 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.55+8255_55+8256ins others(24): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTCTTT others(18): Show |
1 | a0001c0001t0001g0318 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55+8255_55+8256ins others(25): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02074.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.55+8261_55+8270dup others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0320 |
2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.55+8260_55+8270dup others(11): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.55+8259_55+8270dup others(12): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTTTTT others(6): Show |
17 | a0001c0001t0001g0199 a0001c0001t0001g0206 a0001c0001t0001g0207 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.55+8258_55+8270dup others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTTTTT others(7): Show |
58 | a0001c0001t0001g0019 a0001c0001t0001g0159 a0001c0001t0001g0160 others(55): Show |
58 | HG00558.hp2 HG01074.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.55+8257_55+8270dup others(14): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTTTTT others(8): Show |
60 | a0001c0001t0001g0004 a0001c0001t0001g0156 a0001c0001t0001g0157 others(57): Show |
60 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.55+8256_55+8270dup others(15): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758208 | C | CTTTTTTT others(9): Show |
25 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0182 others(22): Show |
25 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.55+8255_55+8270dup others(16): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758208 | ||||||
| chr6:149758212 | T | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(25): Show |
28 | HG00099.hp1 HG01192.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.55+8256T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758212 | |||||||
| chr6:149758226 | T | TTTTTTTT others(6): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.55+8270_55+8271ins others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758226 | |||||||
| chr6:149758226 | T | TTTTTTTT others(8): Show |
1 | a0001c0001t0001g0329 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.55+8270_55+8271ins others(15): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758226 | |||||||
| chr6:149758355 | C | A | 1 | a0002c0002t0002g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.55+8399C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758355 | |||||||
| chr6:149758385 | AT | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+8435delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149758385 | ||||||
| chr6:149758387 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+8431T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758387 | |||||||
| chr6:149758502 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+8546A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758502 | |||||||
| chr6:149758687 | T | C | 108 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(105): Show |
108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.55+8731T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758687 | |||||||
| chr6:149758699 | A | G | 108 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(105): Show |
108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.55+8743A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758699 | |||||||
| chr6:149758739 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
183 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.55+8783G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758739 | |||||||
| chr6:149758786 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55+8830G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758786 | |||||||
| chr6:149758843 | A | T | 1 | a0001c0001t0001g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.55+8887A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758843 | |||||||
| chr6:149758875 | A | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+8919A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758875 | |||||||
| chr6:149758881 | T | C | 108 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(105): Show |
108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.55+8925T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758881 | |||||||
| chr6:149758953 | G | A | 2 | a0002c0002t0002g0001 a0002c0002t0002g0027 |
3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.55+8997G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149758953 | |||||||
| chr6:149759123 | GCTCGGCC others(613): Show |
G | 4 | a0002c0002t0002g0093 a0002c0002t0002g0095 a0002c0002t0002g0096 others(1): Show |
4 | HG01358.hp1 HG02040.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+9208_55+9827del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149759123 | ||||||
| chr6:149759126 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.55+9170C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759126 | |||||||
| chr6:149759141 | C | T | 4 | a0001c0001t0001g0238 a0001c0001t0001g0242 a0001c0001t0001g0277 others(1): Show |
4 | NA18964.hp2 NA18968.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+9185C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759141 | |||||||
| chr6:149759170 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0330 |
3 | HG01884.hp2 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.55+9214C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759170 | |||||||
| chr6:149759332 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.55+9376G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759332 | |||||||
| chr6:149759454 | T | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+9498T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759454 | |||||||
| chr6:149759550 | A | C | 4 | a0002c0002t0002g0024 a0002c0002t0002g0025 a0002c0002t0002g0026 others(1): Show |
4 | HG00323.hp2 HG01361.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+9594A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759550 | |||||||
| chr6:149759746 | C | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.55+9790C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759746 | |||||||
| chr6:149759774 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55+9818C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759774 | |||||||
| chr6:149759786 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55+9830C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149759786 | |||||||
| chr6:149760020 | T | TA | 12 | a0002c0002t0002g0089 a0002c0002t0002g0090 a0002c0002t0002g0091 others(9): Show |
12 | HG01358.hp1 HG02040.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.55+10065dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149760020 | ||||||
| chr6:149760331 | A | G | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.55+10375A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149760331 | |||||||
| chr6:149760522 | G | A | 1 | a0002c0002t0002g0032 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.55+10566G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149760522 | |||||||
| chr6:149760784 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-10378G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149760784 | |||||||
| chr6:149760806 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.56-10356C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149760806 | |||||||
| chr6:149760843 | C | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-10319C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149760843 | |||||||
| chr6:149760959 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.56-10203A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149760959 | |||||||
| chr6:149761026 | A | AGT | 17 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00733.hp1 HG01192.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.56-10109_56-10108d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761026 | ||||||
| chr6:149761026 | AGT | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0132 a0002c0002t0002g0094 |
3 | NA18952.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.56-10109_56-10108d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761026 | ||||||
| chr6:149761026 | AGTGTGT | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0163 a0001c0001t0001g0167 others(14): Show |
17 | HG00558.hp2 HG00639.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.56-10113_56-10108d others(8): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761026 | ||||||
| chr6:149761026 | AGTGTGTG others(1): Show |
A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
155 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.56-10115_56-10108d others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761026 | ||||||
| chr6:149761026 | AGTGTGTG others(3): Show |
A | 22 | a0001c0001t0001g0018 a0001c0001t0001g0154 a0001c0001t0001g0206 others(19): Show |
22 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.56-10117_56-10108d others(12): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761026 | ||||||
| chr6:149761108 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.56-10054T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149761108 | |||||||
| chr6:149761178 | T | TAC | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.56-9968_56-9967dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761178 | ||||||
| chr6:149761178 | T | TACACAC | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-9972_56-9967dup others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761178 | ||||||
| chr6:149761257 | ATGTG | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
192 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.56-9885_56-9882del others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761257 | ||||||
| chr6:149761296 | CAT | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-9864_56-9863del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149761296 | ||||||
| chr6:149761375 | G | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.56-9787G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149761375 | |||||||
| chr6:149761481 | A | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0222 others(1): Show |
4 | HG02055.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-9681A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149761481 | |||||||
| chr6:149761576 | A | G | 68 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0198 others(65): Show |
68 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.56-9586A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149761576 | |||||||
| chr6:149761754 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.56-9408C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149761754 | |||||||
| chr6:149761920 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-9242C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149761920 | |||||||
| chr6:149761995 | A | G | 2 | a0002c0002t0002g0050 a0002c0002t0002g0051 |
2 | HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.56-9167A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149761995 | |||||||
| chr6:149762085 | A | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(162): Show |
165 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.56-9077A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762085 | |||||||
| chr6:149762280 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.56-8882A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762280 | |||||||
| chr6:149762390 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.56-8772A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762390 | |||||||
| chr6:149762436 | C | G | 3 | a0001c0001t0001g0297 a0001c0001t0001g0301 a0001c0001t0001g0309 |
3 | HG00741.hp2 HG02145.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.56-8726C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762436 | |||||||
| chr6:149762485 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-8677T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762485 | |||||||
| chr6:149762501 | TATATATA others(226): Show |
T | 1 | a0002c0002t0002g0033 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.56-8634_56-8402del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762501 | ||||||
| chr6:149762505 | TATATATA others(487): Show |
T | 1 | a0001c0001t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.56-8648_56-8155del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762505 | ||||||
| chr6:149762507 | TATATATC others(509): Show |
T | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56-8639_56-8124del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762507 | ||||||
| chr6:149762514 | CTATGATA others(130): Show |
C | 2 | a0002c0002t0002g0001 a0002c0002t0002g0027 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.56-8618_56-8482del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762514 | ||||||
| chr6:149762518 | G | GATATATA others(80): Show |
1 | a0002c0002t0002g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.56-8619_56-8618ins others(87): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762518 | ||||||
| chr6:149762518 | GATATAT | G | 14 | a0001c0001t0001g0018 a0001c0001t0001g0127 a0001c0001t0001g0154 others(11): Show |
14 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.56-8639_56-8634del others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762518 | ||||||
| chr6:149762518 | GATATATA others(76): Show |
G | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.56-8639_56-8557del others(83): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762518 | ||||||
| chr6:149762518 | GATATATA others(326): Show |
G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8639_56-8307del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762518 | ||||||
| chr6:149762520 | TATATATA others(21): Show |
T | 1 | a0002c0002t0002g0070 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.56-8633_56-8606del others(28): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762520 | ||||||
| chr6:149762535 | TATATATA others(6): Show |
T | 1 | a0002c0002t0002g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.56-8618_56-8606del others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762535 | ||||||
| chr6:149762537 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56-8625T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762537 | |||||||
| chr6:149762540 | ATATC | A | 3 | a0001c0001t0001g0272 a0001c0001t0001g0296 a0001c0001t0004g0219 |
3 | HG03831.hp1 NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.56-8618_56-8615del others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762540 | ||||||
| chr6:149762540 | ATATCTAT others(415): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-8618_56-8197del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762540 | ||||||
| chr6:149762540 | ATATCTAT others(537): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56-8618_56-8075del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762540 | ||||||
| chr6:149762543 | TCTATGAT others(5): Show |
T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-8618_56-8607del others(12): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762543 | |||||||
| chr6:149762543 | TCTATGAT others(352): Show |
T | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-8618_56-8260del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762543 | |||||||
| chr6:149762543 | TCTATGAT others(391): Show |
T | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.56-8618_56-8221del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762543 | |||||||
| chr6:149762543 | TCTATGAT others(552): Show |
T | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-8618_56-8060del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762543 | |||||||
| chr6:149762543 | TCTATGAT others(567): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-8618_56-8045del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762543 | |||||||
| chr6:149762544 | C | CTATGATA others(61): Show |
1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.56-8604_56-8603ins others(68): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762544 | ||||||
| chr6:149762548 | G | GAT | 68 | a0002c0002t0002g0001 a0002c0002t0002g0024 a0002c0002t0002g0025 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.56-8603_56-8602dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762548 | ||||||
| chr6:149762548 | G | GATATATA others(29): Show |
1 | a0002c0002t0002g0097 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.56-8602_56-8601ins others(36): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762548 | ||||||
| chr6:149762548 | G | GATATATA others(55): Show |
2 | a0002c0002t0002g0038 a0002c0002t0002g0039 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.56-8602_56-8601ins others(62): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762548 | ||||||
| chr6:149762548 | G | GATATATA others(10): Show |
1 | a0002c0002t0002g0040 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.56-8604_56-8603ins others(17): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762548 | ||||||
| chr6:149762549 | ATATATAT others(2): Show |
A | 3 | a0001c0001t0001g0272 a0001c0001t0001g0296 a0001c0001t0004g0219 |
3 | HG03831.hp1 NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.56-8612_56-8604del others(9): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762549 | |||||||
| chr6:149762550 | T | TATATATA others(10): Show |
3 | a0002c0002t0002g0031 a0002c0002t0002g0094 a0002c0002t0002g0107 |
3 | NA18944.hp1 NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.56-8602_56-8601ins others(17): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762550 | ||||||
| chr6:149762550 | T | TATATATA others(40): Show |
1 | a0002c0002t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56-8602_56-8601ins others(47): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762550 | ||||||
| chr6:149762550 | T | TATATATA others(42): Show |
3 | a0002c0002t0002g0036 a0002c0002t0002g0103 a0002c0002t0002g0104 |
3 | HG00642.hp1 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.56-8572_56-8571ins others(49): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762550 | ||||||
| chr6:149762550 | T | TATATATA others(25): Show |
1 | a0002c0002t0002g0032 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.56-8604_56-8603ins others(32): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762550 | ||||||
| chr6:149762550 | T | TATATATA others(55): Show |
1 | a0002c0002t0002g0052 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.56-8604_56-8603ins others(62): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762550 | ||||||
| chr6:149762552 | TATATATA others(6): Show |
T | 1 | a0002c0002t0002g0113 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.56-8601_56-8589del others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762552 | ||||||
| chr6:149762552 | TATATATA others(21): Show |
T | 1 | a0002c0002t0002g0089 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.56-8601_56-8574del others(28): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762552 | ||||||
| chr6:149762556 | T | G | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-8606T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762556 | |||||||
| chr6:149762561 | C | A | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.56-8601C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762561 | |||||||
| chr6:149762580 | G | GATAT | 4 | a0002c0002t0002g0047 a0002c0002t0002g0048 a0002c0002t0002g0049 others(1): Show |
4 | HG00140.hp1 HG00323.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8575_56-8572dup others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762580 | ||||||
| chr6:149762580 | GATATAT | G | 8 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(5): Show |
8 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-8577_56-8572del others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762580 | ||||||
| chr6:149762606 | CTATGATA others(81): Show |
C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0296 |
2 | NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.56-8552_56-8465del others(88): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762606 | ||||||
| chr6:149762610 | GATATATA others(1): Show |
G | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8547_56-8540del others(8): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762610 | ||||||
| chr6:149762610 | GATATATA others(29): Show |
G | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-8543_56-8508del others(36): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762610 | ||||||
| chr6:149762610 | GATATATA others(78): Show |
G | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.56-8547_56-8463del others(85): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762610 | ||||||
| chr6:149762612 | T | TATATATA others(6): Show |
3 | a0002c0002t0002g0047 a0002c0002t0002g0085 a0002c0002t0002g0111 |
3 | HG00140.hp1 HG00323.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.56-8542_56-8541ins others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762612 | ||||||
| chr6:149762627 | GAT | G | 7 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(4): Show |
7 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-8524_56-8523del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762627 | ||||||
| chr6:149762629 | T | TATATATA others(6): Show |
1 | a0002c0002t0002g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.56-8525_56-8524ins others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762629 | ||||||
| chr6:149762631 | TATATATA others(6): Show |
T | 3 | a0002c0002t0002g0001 a0002c0002t0002g0035 a0002c0002t0002g0102 |
3 | HG00280.hp1 HG01516.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.56-8522_56-8510del others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762631 | ||||||
| chr6:149762635 | T | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8527T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762635 | |||||||
| chr6:149762640 | CTATGATA others(4): Show |
C | 1 | a0002c0002t0002g0088 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.56-8507_56-8497del others(11): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762640 | ||||||
| chr6:149762651 | A | ATATATC | 5 | a0002c0002t0002g0038 a0002c0002t0002g0039 a0002c0002t0002g0047 others(2): Show |
5 | HG00140.hp1 HG00323.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-8508_56-8507ins others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762651 | ||||||
| chr6:149762651 | A | ATATATCT others(14): Show |
4 | a0002c0002t0002g0093 a0002c0002t0002g0095 a0002c0002t0002g0096 others(1): Show |
4 | HG01358.hp1 HG02040.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8508_56-8507ins others(21): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762651 | ||||||
| chr6:149762651 | A | ATATATCT others(61): Show |
1 | a0002c0002t0002g0067 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.56-8508_56-8507ins others(68): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762651 | ||||||
| chr6:149762651 | A | ATATC | 75 | a0002c0002t0002g0024 a0002c0002t0002g0025 a0002c0002t0002g0026 others(72): Show |
75 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.56-8508_56-8507ins others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762651 | ||||||
| chr6:149762651 | A | C | 5 | a0001c0001t0001g0250 a0001c0001t0004g0219 a0002c0002t0002g0001 others(2): Show |
5 | HG00280.hp1 HG01516.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-8511A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762651 | |||||||
| chr6:149762655 | G | GATATATA others(10): Show |
5 | a0002c0002t0002g0037 a0002c0002t0002g0043 a0002c0002t0002g0053 others(2): Show |
5 | HG01255.hp2 HG02683.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-8464_56-8448dup others(17): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762655 | ||||||
| chr6:149762655 | G | T | 1 | a0002c0002t0002g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.56-8507G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762655 | |||||||
| chr6:149762661 | T | A | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-8501T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762661 | |||||||
| chr6:149762661 | T | G | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8501T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762661 | |||||||
| chr6:149762670 | GAT | G | 10 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(7): Show |
10 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-8481_56-8480del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762670 | ||||||
| chr6:149762672 | T | TATATATA others(25): Show |
1 | a0002c0002t0002g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.56-8464_56-8433dup others(32): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762672 | ||||||
| chr6:149762678 | T | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8484T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762678 | |||||||
| chr6:149762687 | GAT | G | 11 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(8): Show |
11 | HG01243.hp2 HG03041.hp1 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-8464_56-8463del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762687 | ||||||
| chr6:149762689 | T | TATATATA others(8): Show |
4 | a0002c0002t0002g0045 a0002c0002t0002g0060 a0002c0002t0002g0081 others(1): Show |
4 | HG00733.hp2 HG02572.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-8432_56-8418dup others(15): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762689 | ||||||
| chr6:149762689 | T | TATATATA others(25): Show |
1 | a0002c0002t0002g0082 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.56-8448_56-8447ins others(32): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762689 | ||||||
| chr6:149762689 | T | TATATATA others(23): Show |
1 | a0002c0002t0002g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.56-8447_56-8418dup others(30): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762689 | ||||||
| chr6:149762689 | T | TATATATA others(57): Show |
2 | a0002c0002t0002g0048 a0002c0002t0002g0049 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.56-8410_56-8409ins others(64): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762689 | ||||||
| chr6:149762689 | T | TATATATA others(21): Show |
1 | a0002c0002t0002g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.56-8465_56-8464ins others(28): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762689 | ||||||
| chr6:149762695 | T | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8467T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762695 | |||||||
| chr6:149762695 | T | G | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-8467T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762695 | |||||||
| chr6:149762704 | G | GATATATA others(46): Show |
1 | a0002c0002t0002g0059 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.56-8448_56-8447ins others(53): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762704 | ||||||
| chr6:149762710 | T | A | 8 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(5): Show |
8 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-8452T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762710 | |||||||
| chr6:149762711 | A | ATATATCT others(10): Show |
1 | a0002c0002t0002g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.56-8448_56-8447ins others(17): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762711 | ||||||
| chr6:149762725 | T | G | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.56-8437T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762725 | |||||||
| chr6:149762725 | TATATCTA others(550): Show |
T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-8417_56-7861del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762725 | ||||||
| chr6:149762729 | T | C | 1 | a0002c0002t0002g0052 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.56-8433T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762729 | |||||||
| chr6:149762729 | T | TATCTATG others(27): Show |
1 | a0002c0002t0002g0086 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.56-8433_56-8432ins others(34): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762729 | |||||||
| chr6:149762734 | GAT | G | 4 | a0001c0001t0001g0250 a0001c0001t0001g0319 a0001c0001t0004g0219 others(1): Show |
4 | HG00738.hp2 HG03516.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-8417_56-8416del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762734 | ||||||
| chr6:149762739 | ATATATAT others(463): Show |
A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0296 |
2 | NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.56-8422_56-7953del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762739 | |||||||
| chr6:149762742 | T | G | 2 | a0001c0001t0001g0319 a0001c0001t0004g0219 |
2 | HG03516.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.56-8420T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762742 | |||||||
| chr6:149762746 | T | C | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-8416T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762746 | |||||||
| chr6:149762757 | T | A | 2 | a0001c0001t0001g0319 a0001c0001t0004g0219 |
2 | HG03516.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.56-8405T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762757 | |||||||
| chr6:149762757 | T | G | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.56-8405T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762757 | |||||||
| chr6:149762761 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0004g0219 |
2 | HG03516.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.56-8401C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762761 | |||||||
| chr6:149762772 | T | A | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.56-8390T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762772 | |||||||
| chr6:149762776 | TAC | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0319 a0001c0001t0004g0219 |
3 | HG03516.hp1 HG03831.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.56-8385_56-8384del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762776 | |||||||
| chr6:149762789 | T | G | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-8373T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762789 | |||||||
| chr6:149762789 | TATACCTA others(486): Show |
T | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.56-8369_56-7877del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762789 | ||||||
| chr6:149762793 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.56-8369C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762793 | |||||||
| chr6:149762804 | T | A | 2 | a0001c0001t0001g0319 a0001c0001t0004g0219 |
2 | HG03516.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.56-8358T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762804 | |||||||
| chr6:149762816 | AATCTATG others(455): Show |
A | 2 | a0001c0001t0001g0319 a0001c0001t0004g0219 |
2 | HG03516.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.56-8345_56-7884del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762816 | |||||||
| chr6:149762834 | TATATATA others(6): Show |
T | 7 | a0002c0002t0002g0024 a0002c0002t0002g0025 a0002c0002t0002g0026 others(4): Show |
7 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-8306_56-8294del others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762834 | ||||||
| chr6:149762842 | T | C | 1 | a0002c0002t0002g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.56-8320T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762842 | |||||||
| chr6:149762847 | GATATATA others(8): Show |
G | 1 | a0002c0002t0002g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.56-8293_56-8279del others(15): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762847 | ||||||
| chr6:149762862 | T | TATATATA others(30): Show |
3 | a0002c0002t0002g0061 a0002c0002t0002g0068 a0002c0002t0002g0332 |
3 | HG01243.hp2 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.56-8278_56-8242dup others(37): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762862 | ||||||
| chr6:149762862 | T | TATATATA others(67): Show |
1 | a0002c0002t0002g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.56-8242_56-8241ins others(74): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762862 | ||||||
| chr6:149762867 | ATATC | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8291_56-8288del others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762867 | ||||||
| chr6:149762876 | AT | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8285delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762876 | |||||||
| chr6:149762880 | A | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8282A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762880 | |||||||
| chr6:149762885 | T | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8277T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762885 | |||||||
| chr6:149762899 | GATAT | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8258_56-8255del others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762899 | ||||||
| chr6:149762899 | GATATATA others(8): Show |
G | 4 | a0002c0002t0002g0089 a0002c0002t0002g0090 a0002c0002t0002g0091 others(1): Show |
4 | NA18960.hp1 NA18980.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-8241_56-8227del others(15): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762899 | ||||||
| chr6:149762903 | T | G | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-8259T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762903 | |||||||
| chr6:149762931 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0136 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.56-8231T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762931 | |||||||
| chr6:149762932 | A | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.56-8230A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762932 | |||||||
| chr6:149762942 | T | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8220T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762942 | |||||||
| chr6:149762942 | T | G | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.56-8220T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762942 | |||||||
| chr6:149762947 | C | CTATGATA others(17): Show |
1 | a0002c0002t0002g0095 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.56-8206_56-8183dup others(24): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762947 | ||||||
| chr6:149762956 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.56-8206G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762956 | |||||||
| chr6:149762956 | G | GTATATCT others(17): Show |
10 | a0002c0002t0002g0057 a0002c0002t0002g0058 a0002c0002t0002g0059 others(7): Show |
10 | HG00280.hp2 HG00642.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-8156_56-8133dup others(24): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762956 | ||||||
| chr6:149762956 | G | GTATATCT others(41): Show |
3 | a0002c0002t0002g0054 a0002c0002t0002g0080 a0002c0002t0002g0087 |
3 | HG01109.hp2 HG01192.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.56-8180_56-8133dup others(48): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762956 | ||||||
| chr6:149762956 | GTATATCT others(17): Show |
G | 1 | a0002c0002t0002g0075 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.56-8156_56-8133del others(24): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149762956 | ||||||
| chr6:149762964 | A | G | 4 | a0002c0002t0002g0034 a0002c0002t0002g0061 a0002c0002t0002g0068 others(1): Show |
4 | HG01243.hp2 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-8198A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762964 | |||||||
| chr6:149762971 | A | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0320 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.56-8191A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762971 | |||||||
| chr6:149762971 | ATATGATA others(231): Show |
A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.56-8190_56-7953del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762971 | |||||||
| chr6:149762995 | A | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0320 a0001c0001t0001g0330 |
3 | HG01884.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.56-8167A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149762995 | |||||||
| chr6:149763005 | T | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.56-8157T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763005 | |||||||
| chr6:149763019 | A | ATATGATA others(37): Show |
1 | a0002c0002t0002g0088 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.56-8133_56-8132ins others(44): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763019 | ||||||
| chr6:149763019 | A | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0270 |
2 | HG02717.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.56-8143A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763019 | |||||||
| chr6:149763019 | ATATGATA others(7): Show |
A | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-8142_56-8129del others(14): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763019 | |||||||
| chr6:149763020 | TATGATAT others(7): Show |
T | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.56-8139_56-8126del others(14): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763020 | ||||||
| chr6:149763030 | C | A | 1 | a0001c0001t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.56-8132C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763030 | |||||||
| chr6:149763034 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-8128G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763034 | |||||||
| chr6:149763039 | C | A | 1 | a0002c0002t0002g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.56-8123C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763039 | |||||||
| chr6:149763044 | ATATGTAT others(66): Show |
A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56-8114_56-8042del others(73): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763044 | ||||||
| chr6:149763048 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0270 a0001c0001t0001g0320 others(1): Show |
4 | HG01884.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-8114G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763048 | |||||||
| chr6:149763049 | T | A | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-8113T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763049 | |||||||
| chr6:149763049 | T | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.56-8113T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763049 | |||||||
| chr6:149763054 | C | CTATGATA others(32): Show |
2 | a0002c0002t0002g0065 a0002c0002t0002g0084 |
2 | HG01261.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.56-8045_56-8007dup others(39): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763054 | ||||||
| chr6:149763064 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.56-8098T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763064 | |||||||
| chr6:149763064 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.56-8098T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763064 | |||||||
| chr6:149763078 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0270 a0001c0001t0001g0320 others(1): Show |
4 | HG01884.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-8084G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763078 | |||||||
| chr6:149763079 | T | A | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-8083T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763079 | |||||||
| chr6:149763079 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-8083T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763079 | |||||||
| chr6:149763093 | A | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0270 |
2 | HG02109.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.56-8069A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763093 | |||||||
| chr6:149763093 | ATATGATA others(109): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-8068_56-7953del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763093 | |||||||
| chr6:149763093 | ATATGATA others(157): Show |
A | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-8068_56-7905del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763093 | |||||||
| chr6:149763094 | TATGATAT others(157): Show |
T | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.56-8065_56-7902del | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763094 | ||||||
| chr6:149763103 | T | A | 1 | a0001c0001t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.56-8059T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763103 | |||||||
| chr6:149763103 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-8059T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763103 | |||||||
| chr6:149763117 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0270 |
2 | NA19007.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-8045G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763117 | |||||||
| chr6:149763118 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-8044T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763118 | |||||||
| chr6:149763123 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56-8039C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763123 | |||||||
| chr6:149763132 | A | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0210 |
2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-8030A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763132 | |||||||
| chr6:149763132 | ATATGATA others(70): Show |
A | 1 | a0001c0001t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.56-8029_56-7953del others(77): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763132 | |||||||
| chr6:149763139 | A | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0154 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.56-8023A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763139 | |||||||
| chr6:149763142 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-8020T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763142 | |||||||
| chr6:149763164 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0154 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.56-7998G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763164 | |||||||
| chr6:149763200 | ATATATCT others(2): Show |
A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01109.hp1 HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-7961_56-7953del others(9): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763200 | |||||||
| chr6:149763201 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56-7961T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763201 | |||||||
| chr6:149763215 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56-7947C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763215 | |||||||
| chr6:149763225 | AATATCTA others(2): Show |
A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.56-7923_56-7915del others(9): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763225 | ||||||
| chr6:149763238 | TCTATG | T | 5 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0185 others(2): Show |
5 | HG02523.hp2 NA18967.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-7923_56-7919del others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763238 | |||||||
| chr6:149763238 | TCTATGAT others(11): Show |
T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-7923_56-7906del others(18): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763238 | |||||||
| chr6:149763242 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.56-7920T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763242 | |||||||
| chr6:149763248 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.56-7914A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763248 | |||||||
| chr6:149763249 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56-7913T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763249 | |||||||
| chr6:149763250 | A | C | 5 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0185 others(2): Show |
5 | HG02523.hp2 NA18967.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-7912A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763250 | |||||||
| chr6:149763253 | T | TG | 5 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0185 others(2): Show |
5 | HG02523.hp2 NA18967.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-7909_56-7908ins others(1): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763253 | |||||||
| chr6:149763254 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.56-7908C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763254 | |||||||
| chr6:149763257 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-7905T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763257 | |||||||
| chr6:149763257 | T | TA | 5 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0185 others(2): Show |
5 | HG02523.hp2 NA18967.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-7905_56-7904ins others(1): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763257 | |||||||
| chr6:149763258 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-7904G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763258 | |||||||
| chr6:149763262 | T | C | 6 | a0001c0001t0001g0132 a0001c0001t0001g0168 a0001c0001t0001g0175 others(3): Show |
6 | HG02523.hp2 NA18967.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-7900T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763262 | |||||||
| chr6:149763262 | T | TAGATAC | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.56-7900_56-7899ins others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763262 | |||||||
| chr6:149763272 | AAATATCT others(2): Show |
A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01109.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.56-7889_56-7881del others(9): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763272 | |||||||
| chr6:149763278 | CTA | C | 3 | a0002c0002t0002g0032 a0002c0002t0002g0052 a0002c0002t0002g0086 |
3 | NA18945.hp2 NA19009.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.56-7882_56-7881del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763278 | ||||||
| chr6:149763282 | G | GATATAT | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.56-7876_56-7875ins others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149763282 | ||||||
| chr6:149763282 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-7880G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763282 | |||||||
| chr6:149763287 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.56-7875C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763287 | |||||||
| chr6:149763297 | T | A | 2 | a0002c0002t0002g0065 a0002c0002t0002g0069 |
2 | HG00280.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.56-7865T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763297 | |||||||
| chr6:149763297 | T | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01109.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.56-7865T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763297 | |||||||
| chr6:149763311 | A | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
5 | HG01109.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-7851A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763311 | |||||||
| chr6:149763311 | A | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.56-7851A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763311 | |||||||
| chr6:149763351 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-7811G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763351 | |||||||
| chr6:149763714 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-7448A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763714 | |||||||
| chr6:149763754 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.56-7408T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763754 | |||||||
| chr6:149763904 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG00099.hp1 HG02080.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-7258T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763904 | |||||||
| chr6:149763997 | A | G | 2 | a0002c0002t0002g0046 a0002c0002t0002g0105 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.56-7165A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149763997 | |||||||
| chr6:149764102 | G | T | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-7060G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764102 | |||||||
| chr6:149764150 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.56-7012G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764150 | |||||||
| chr6:149764380 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02895.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.56-6782G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764380 | |||||||
| chr6:149764481 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.56-6681G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764481 | |||||||
| chr6:149764521 | G | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-6641G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764521 | |||||||
| chr6:149764529 | A | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-6633A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764529 | |||||||
| chr6:149764597 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.56-6565G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764597 | |||||||
| chr6:149764634 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.56-6528G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764634 | |||||||
| chr6:149764873 | C | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-6289C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764873 | |||||||
| chr6:149764913 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.56-6249T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764913 | |||||||
| chr6:149764993 | A | G | 3 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0007g0289 |
3 | HG01081.hp2 HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.56-6169A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149764993 | |||||||
| chr6:149765291 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.56-5871T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765291 | |||||||
| chr6:149765359 | C | CA | 7 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(4): Show |
7 | HG00140.hp1 HG01516.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-5783dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765359 | ||||||
| chr6:149765359 | C | CAA | 14 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(11): Show |
15 | HG00733.hp1 HG01109.hp1 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.56-5784_56-5783dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765359 | ||||||
| chr6:149765359 | C | CAAA | 48 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
48 | HG00099.hp1 HG01069.hp2 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.56-5785_56-5783dup others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765359 | ||||||
| chr6:149765359 | C | CAAAA | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(143): Show |
146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.56-5786_56-5783dup others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765359 | ||||||
| chr6:149765359 | C | CAAAAA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
27 | HG00741.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.56-5787_56-5783dup others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765359 | ||||||
| chr6:149765592 | T | C | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.56-5570T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765592 | |||||||
| chr6:149765650 | TTTTTTTA | T | 4 | a0001c0001t0008g0294 a0002c0002t0002g0033 a0002c0002t0002g0045 others(1): Show |
4 | NA18951.hp1 NA19060.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-5484_56-5478del others(7): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765650 | ||||||
| chr6:149765652 | T | C | 1 | a0002c0002t0002g0067 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.56-5510T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765652 | |||||||
| chr6:149765703 | A | C | 1 | a0002c0002t0002g0081 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.56-5459A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765703 | |||||||
| chr6:149765718 | G | C | 1 | a0001c0001t0001g0329 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.56-5444G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765718 | |||||||
| chr6:149765831 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-5331C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765831 | |||||||
| chr6:149765920 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.56-5242C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765920 | |||||||
| chr6:149765976 | A | T | 1 | a0001c0001t0001g0331 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.56-5186A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765976 | |||||||
| chr6:149765977 | T | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0331 |
2 | HG01169.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.56-5185T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765977 | |||||||
| chr6:149765978 | A | T | 1 | a0001c0001t0001g0235 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.56-5184A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765978 | |||||||
| chr6:149765979 | A | AT | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(40): Show |
43 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.56-5183_56-5182ins others(1): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765979 | |||||||
| chr6:149765979 | A | ATT | 5 | a0001c0001t0001g0226 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
5 | NA18947.hp2 NA18960.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-5183_56-5182ins others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765979 | |||||||
| chr6:149765979 | A | T | 1 | a0001c0001t0001g0331 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.56-5183A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765979 | |||||||
| chr6:149765980 | A | AT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.56-5167dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765980 | ||||||
| chr6:149765980 | A | ATT | 7 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0210 others(4): Show |
7 | HG01516.hp2 HG01517.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-5168_56-5167dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149765980 | ||||||
| chr6:149765980 | A | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(46): Show |
49 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.56-5182A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149765980 | |||||||
| chr6:149766383 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-4779G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766383 | |||||||
| chr6:149766440 | A | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-4722A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766440 | |||||||
| chr6:149766491 | C | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-4671C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766491 | |||||||
| chr6:149766530 | A | G | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-4632A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766530 | |||||||
| chr6:149766607 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.56-4555T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766607 | |||||||
| chr6:149766648 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-4514G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766648 | |||||||
| chr6:149766670 | G | A | 2 | a0002c0002t0002g0054 a0002c0002t0002g0087 |
2 | HG01109.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.56-4492G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766670 | |||||||
| chr6:149766749 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.56-4413C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766749 | |||||||
| chr6:149766795 | C | T | 3 | a0002c0002t0002g0090 a0002c0002t0002g0091 a0002c0002t0002g0092 |
3 | NA18980.hp2 NA19004.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.56-4367C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766795 | |||||||
| chr6:149766817 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.56-4345C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766817 | |||||||
| chr6:149766848 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-4314C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149766848 | |||||||
| chr6:149767024 | C | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-4138C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767024 | |||||||
| chr6:149767081 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-4081C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767081 | |||||||
| chr6:149767176 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.56-3986C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767176 | |||||||
| chr6:149767258 | C | CT | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.56-3892dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149767258 | ||||||
| chr6:149767436 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-3726T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767436 | |||||||
| chr6:149767451 | A | AATTTTT | 3 | a0002c0002t0002g0036 a0002c0002t0002g0103 a0002c0002t0002g0104 |
3 | HG00642.hp1 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.56-3700_56-3695dup others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149767451 | ||||||
| chr6:149767481 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-3681T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767481 | |||||||
| chr6:149767493 | C | T | 1 | a0002c0002t0002g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.56-3669C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767493 | |||||||
| chr6:149767547 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-3615A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767547 | |||||||
| chr6:149767567 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56-3595C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767567 | |||||||
| chr6:149767794 | TGTTC | T | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0215 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-3364_56-3361del others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149767794 | ||||||
| chr6:149767798 | CGTTT | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.56-3355_56-3352del others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149767798 | ||||||
| chr6:149767816 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-3346T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767816 | |||||||
| chr6:149767854 | C | T | 1 | a0002c0002t0002g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.56-3308C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767854 | |||||||
| chr6:149767886 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-3276C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767886 | |||||||
| chr6:149767991 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.56-3171G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149767991 | |||||||
| chr6:149768013 | T | TA | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-3146dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149768013 | ||||||
| chr6:149768130 | TG | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-3031delG | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768130 | |||||||
| chr6:149768134 | C | G | 1 | a0002c0002t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56-3028C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768134 | |||||||
| chr6:149768273 | A | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.56-2889A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768273 | |||||||
| chr6:149768385 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.56-2777C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768385 | |||||||
| chr6:149768408 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.56-2754C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768408 | |||||||
| chr6:149768412 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.56-2750T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768412 | |||||||
| chr6:149768444 | A | AT | 9 | a0002c0002t0002g0044 a0002c0002t0002g0054 a0002c0002t0002g0055 others(6): Show |
9 | HG01099.hp1 HG01192.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-2693dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149768444 | ||||||
| chr6:149768444 | AT | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0023 others(20): Show |
23 | HG00140.hp2 HG01109.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.56-2693delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149768444 | ||||||
| chr6:149768444 | ATT | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.56-2694_56-2693del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149768444 | ||||||
| chr6:149768444 | ATTT | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(15): Show |
18 | HG00558.hp2 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.56-2695_56-2693del others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149768444 | ||||||
| chr6:149768605 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.56-2557C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768605 | |||||||
| chr6:149768637 | T | C | 3 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0007g0289 |
3 | HG01081.hp2 HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.56-2525T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768637 | |||||||
| chr6:149768711 | C | T | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0129 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-2451C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768711 | |||||||
| chr6:149768819 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.56-2343G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149768819 | |||||||
| chr6:149769130 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.56-2032T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769130 | |||||||
| chr6:149769281 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-1881G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769281 | |||||||
| chr6:149769308 | C | CTT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-1831_56-1830dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(1): Show |
49 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0160 others(46): Show |
49 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.56-1837_56-1830dup others(8): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(2): Show |
48 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(45): Show |
48 | HG00741.hp1 HG01081.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.56-1838_56-1830dup others(9): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(3): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
41 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.56-1839_56-1830dup others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(4): Show |
30 | a0001c0001t0001g0005 a0001c0001t0001g0121 a0001c0001t0001g0135 others(27): Show |
30 | HG00099.hp1 HG00423.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.56-1840_56-1830dup others(11): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(5): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(18): Show |
22 | HG00423.hp1 HG02055.hp2 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.56-1841_56-1830dup others(12): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(6): Show |
12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0019 others(9): Show |
12 | HG01192.hp2 HG02056.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.56-1842_56-1830dup others(13): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(7): Show |
7 | a0001c0001t0001g0009 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG01928.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-1843_56-1830dup others(14): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0211 a0001c0001t0009g0145 |
2 | HG00733.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.56-1847_56-1830dup others(18): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | CT | C | 6 | a0001c0001t0001g0251 a0002c0002t0002g0028 a0002c0002t0002g0047 others(3): Show |
6 | HG00323.hp1 HG01099.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-1830delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0002g0101 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.56-1839_56-1830del others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | CTTTTTTT others(4): Show |
C | 14 | a0002c0002t0002g0024 a0002c0002t0002g0025 a0002c0002t0002g0026 others(11): Show |
14 | HG00323.hp2 HG01099.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.56-1840_56-1830del others(11): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769308 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0268 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.56-1841_56-1830del others(12): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769308 | ||||||
| chr6:149769332 | T | TG | 3 | a0002c0002t0002g0043 a0002c0002t0002g0053 a0002c0002t0002g0064 |
3 | NA18966.hp1 NA18968.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.56-1829dupG | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769332 | ||||||
| chr6:149769356 | G | T | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0215 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-1806G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769356 | |||||||
| chr6:149769533 | C | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-1629C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769533 | |||||||
| chr6:149769545 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-1617C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769545 | |||||||
| chr6:149769680 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-1482T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769680 | |||||||
| chr6:149769681 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.56-1481C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769681 | |||||||
| chr6:149769767 | TA | T | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0129 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-1392delA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769767 | ||||||
| chr6:149769770 | A | AT | 9 | a0002c0002t0002g0056 a0002c0002t0002g0063 a0002c0002t0002g0067 others(6): Show |
9 | HG01496.hp1 HG02027.hp2 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-1366dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769770 | ||||||
| chr6:149769770 | AT | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0021 others(33): Show |
36 | HG01175.hp2 HG01975.hp1 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.56-1366delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769770 | ||||||
| chr6:149769770 | ATT | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.56-1367_56-1366del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769770 | ||||||
| chr6:149769770 | ATTT | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0134 others(18): Show |
21 | HG01109.hp1 HG01515.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.56-1368_56-1366del others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769770 | ||||||
| chr6:149769770 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.56-1375_56-1366del others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769770 | ||||||
| chr6:149769770 | ATTTTTTT others(5): Show |
A | 3 | a0002c0002t0002g0033 a0002c0002t0002g0045 a0002c0002t0002g0081 |
3 | NA18951.hp1 NA19060.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.56-1377_56-1366del others(12): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149769770 | ||||||
| chr6:149769988 | T | C | 9 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
9 | HG01192.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-1174T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149769988 | |||||||
| chr6:149770248 | T | C | 1 | a0002c0002t0002g0332 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.56-914T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770248 | |||||||
| chr6:149770596 | C | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-566C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770596 | |||||||
| chr6:149770637 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.56-525C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770637 | |||||||
| chr6:149770654 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-508C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770654 | |||||||
| chr6:149770705 | C | CA | 20 | a0001c0001t0001g0133 a0001c0001t0001g0141 a0001c0001t0001g0152 others(17): Show |
20 | HG01192.hp1 HG01358.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-440dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149770705 | ||||||
| chr6:149770726 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0008g0294 |
2 | HG03453.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.56-436G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770726 | |||||||
| chr6:149770776 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.56-386A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770776 | |||||||
| chr6:149770828 | C | G | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.56-334C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770828 | |||||||
| chr6:149770854 | C | CCCTG | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.56-307_56-306insCT others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149770854 | ||||||
| chr6:149770860 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.56-302G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770860 | |||||||
| chr6:149770891 | C | A | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.56-271C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770891 | |||||||
| chr6:149770948 | G | A | 1 | a0002c0002t0002g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.56-214G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | chr6 | 149770948 | |||||||
| chr6:149771586 | G | A | 1 | a0002c0002t0002g0040 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.160+320G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149771586 | |||||||
| chr6:149771637 | C | T | 1 | a0002c0002t0002g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.160+371C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149771637 | |||||||
| chr6:149771673 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.160+407T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149771673 | |||||||
| chr6:149771682 | A | C | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.160+416A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149771682 | |||||||
| chr6:149771727 | A | G | 1 | a0002c0002t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+461A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149771727 | |||||||
| chr6:149771818 | G | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0001t0001g0244 others(1): Show |
4 | NA18952.hp2 NA18980.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+552G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149771818 | |||||||
| chr6:149772005 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.160+739T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772005 | |||||||
| chr6:149772177 | G | T | 1 | a0002c0002t0002g0079 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.160+911G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772177 | |||||||
| chr6:149772246 | A | G | 1 | a0002c0002t0002g0109 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161-892A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772246 | |||||||
| chr6:149772340 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.161-798A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772340 | |||||||
| chr6:149772456 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-682C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772456 | |||||||
| chr6:149772542 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.161-596C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772542 | |||||||
| chr6:149772546 | C | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.161-592C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772546 | |||||||
| chr6:149772756 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0217 |
2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.161-382G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772756 | |||||||
| chr6:149772783 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.161-355C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772783 | |||||||
| chr6:149772832 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.161-306G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772832 | |||||||
| chr6:149772845 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.161-293G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772845 | |||||||
| chr6:149772877 | C | T | 1 | a0002c0002t0002g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.161-261C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772877 | |||||||
| chr6:149772900 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.161-238C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772900 | |||||||
| chr6:149772907 | C | G | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.161-231C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772907 | |||||||
| chr6:149772951 | A | C | 6 | a0002c0002t0002g0043 a0002c0002t0002g0053 a0002c0002t0002g0062 others(3): Show |
6 | HG01255.hp2 HG02027.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-187A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | chr6 | 149772951 | |||||||
| chr6:149773016 | G | GA | 9 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0192 others(6): Show |
9 | HG01884.hp2 HG02040.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-103dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 149773016 | ||||||
| chr6:149773282 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.192+113T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773282 | |||||||
| chr6:149773334 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.192+165C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773334 | |||||||
| chr6:149773350 | A | AGTTTT | 3 | a0002c0002t0002g0043 a0002c0002t0002g0053 a0002c0002t0002g0064 |
3 | NA18966.hp1 NA18968.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.192+222_192+226dup others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149773350 | ||||||
| chr6:149773350 | AGTTTT | A | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(25): Show |
28 | HG00099.hp1 HG01192.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.192+222_192+226del others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149773350 | ||||||
| chr6:149773350 | AGTTTTGT others(3): Show |
A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0002c0002t0002g0040 |
3 | HG02273.hp1 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.192+217_192+226del others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149773350 | ||||||
| chr6:149773350 | AGTTTTGT others(8): Show |
A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
210 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.192+212_192+226del others(15): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149773350 | ||||||
| chr6:149773410 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(40): Show |
44 | HG00099.hp1 HG00733.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.192+241G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773410 | |||||||
| chr6:149773417 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.192+248C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773417 | |||||||
| chr6:149773421 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.192+252C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773421 | |||||||
| chr6:149773470 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.192+301C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773470 | |||||||
| chr6:149773471 | C | T | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.192+302C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773471 | |||||||
| chr6:149773519 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+350C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773519 | |||||||
| chr6:149773554 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.192+385A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773554 | |||||||
| chr6:149773578 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+409T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773578 | |||||||
| chr6:149773621 | C | T | 8 | a0002c0002t0002g0036 a0002c0002t0002g0044 a0002c0002t0002g0047 others(5): Show |
8 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+452C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773621 | |||||||
| chr6:149773870 | A | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(40): Show |
44 | HG00099.hp1 HG00733.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.192+701A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773870 | |||||||
| chr6:149773933 | T | G | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.192+764T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149773933 | |||||||
| chr6:149774223 | G | GCTTTT | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0215 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+1065_192+1069d others(7): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149774223 | ||||||
| chr6:149774257 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.192+1088T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774257 | |||||||
| chr6:149774272 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.192+1103C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774272 | |||||||
| chr6:149774296 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+1127G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774296 | |||||||
| chr6:149774301 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+1132G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774301 | |||||||
| chr6:149774388 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(2): Show |
5 | HG02109.hp2 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+1219C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774388 | |||||||
| chr6:149774534 | C | G | 3 | a0001c0001t0001g0165 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | HG00639.hp2 HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.192+1365C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774534 | |||||||
| chr6:149774538 | CT | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.192+1386delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149774538 | ||||||
| chr6:149774560 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+1391C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774560 | |||||||
| chr6:149774686 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+1517C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774686 | |||||||
| chr6:149774704 | A | AC | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.192+1536dupC | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149774704 | ||||||
| chr6:149774705 | C | CT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0266 others(4): Show |
7 | HG01175.hp1 HG01884.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+1556dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149774705 | ||||||
| chr6:149774705 | CT | C | 29 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(26): Show |
29 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.192+1556delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149774705 | ||||||
| chr6:149774762 | A | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+1593A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774762 | |||||||
| chr6:149774768 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.192+1599G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774768 | |||||||
| chr6:149774793 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.192+1624G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774793 | |||||||
| chr6:149774898 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.192+1729G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774898 | |||||||
| chr6:149774928 | C | T | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(25): Show |
28 | HG00099.hp1 HG01192.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.192+1759C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149774928 | |||||||
| chr6:149775136 | G | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+1967G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775136 | |||||||
| chr6:149775216 | T | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+2047T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775216 | |||||||
| chr6:149775255 | A | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.192+2086A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775255 | |||||||
| chr6:149775303 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+2134C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775303 | |||||||
| chr6:149775328 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192+2159A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775328 | |||||||
| chr6:149775391 | T | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.192+2222T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775391 | |||||||
| chr6:149775828 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.192+2659C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775828 | |||||||
| chr6:149775882 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.192+2713A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149775882 | |||||||
| chr6:149776084 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192+2915G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776084 | |||||||
| chr6:149776207 | T | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+3038T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776207 | |||||||
| chr6:149776321 | C | CACTGCAA others(112): Show |
1 | a0001c0001t0001g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.192+3159_192+3160i others(121): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149776321 | ||||||
| chr6:149776321 | C | CACTGCAA others(112): Show |
236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.192+3159_192+3160i others(121): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149776321 | ||||||
| chr6:149776390 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
7 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+3221T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776390 | |||||||
| chr6:149776427 | T | A | 1 | a0001c0001t0001g0273 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.192+3258T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776427 | |||||||
| chr6:149776502 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0268 |
2 | NA18960.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.192+3333C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776502 | |||||||
| chr6:149776604 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+3435G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776604 | |||||||
| chr6:149776631 | G | A | 1 | a0002c0002t0002g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.192+3462G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776631 | |||||||
| chr6:149776661 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.192+3492C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776661 | |||||||
| chr6:149776681 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+3512G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776681 | |||||||
| chr6:149776790 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.192+3621A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776790 | |||||||
| chr6:149776919 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192+3750A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149776919 | |||||||
| chr6:149777026 | AG | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(40): Show |
44 | HG00099.hp1 HG00733.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.192+3858delG | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777026 | |||||||
| chr6:149777113 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.192+3944A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777113 | |||||||
| chr6:149777149 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
7 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+3980A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777149 | |||||||
| chr6:149777390 | G | C | 8 | a0002c0002t0002g0036 a0002c0002t0002g0044 a0002c0002t0002g0047 others(5): Show |
8 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+4221G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777390 | |||||||
| chr6:149777465 | T | TAAATG | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+4299_192+4300i others(7): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149777465 | ||||||
| chr6:149777561 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+4392C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777561 | |||||||
| chr6:149777641 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+4472T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777641 | |||||||
| chr6:149777838 | CTCCT | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.192+4688_192+4691d others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149777838 | ||||||
| chr6:149777876 | CT | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.192+4726delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149777876 | ||||||
| chr6:149777876 | CTT | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0206 a0001c0001t0001g0207 others(11): Show |
14 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+4725_192+4726d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149777876 | ||||||
| chr6:149777895 | T | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0192 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+4726T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777895 | |||||||
| chr6:149777987 | C | T | 3 | a0002c0002t0002g0061 a0002c0002t0002g0068 a0002c0002t0002g0332 |
3 | HG01243.hp2 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.192+4818C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149777987 | |||||||
| chr6:149778003 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.192+4834G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778003 | |||||||
| chr6:149778176 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192+5007G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778176 | |||||||
| chr6:149778215 | T | A | 1 | a0002c0002t0002g0106 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.192+5046T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778215 | |||||||
| chr6:149778229 | TTTA | T | 12 | a0002c0002t0002g0089 a0002c0002t0002g0090 a0002c0002t0002g0091 others(9): Show |
12 | HG01358.hp1 HG02040.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+5072_192+5074d others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149778229 | ||||||
| chr6:149778249 | G | A | 57 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0198 others(54): Show |
57 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.192+5080G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778249 | |||||||
| chr6:149778389 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+5220C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778389 | |||||||
| chr6:149778467 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+5298G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778467 | |||||||
| chr6:149778492 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+5323G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778492 | |||||||
| chr6:149778521 | G | A | 1 | a0002c0002t0002g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.192+5352G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778521 | |||||||
| chr6:149778744 | G | A | 10 | a0002c0002t0002g0054 a0002c0002t0002g0057 a0002c0002t0002g0058 others(7): Show |
10 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+5575G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778744 | |||||||
| chr6:149778907 | A | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+5738A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149778907 | |||||||
| chr6:149779105 | C | T | 1 | a0002c0002t0002g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.192+5936C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779105 | |||||||
| chr6:149779111 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.192+5942G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779111 | |||||||
| chr6:149779125 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+5956C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779125 | |||||||
| chr6:149779242 | ATGTAAAA others(1): Show |
A | 109 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(106): Show |
109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.192+6074_192+6081d others(10): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779242 | |||||||
| chr6:149779251 | A | G | 109 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(106): Show |
109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.192+6082A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779251 | |||||||
| chr6:149779254 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.192+6085T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779254 | |||||||
| chr6:149779294 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.192+6125C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779294 | |||||||
| chr6:149779341 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+6172T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779341 | |||||||
| chr6:149779433 | A | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
9 | HG00733.hp1 HG02886.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+6264A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779433 | |||||||
| chr6:149779456 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.192+6287C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779456 | |||||||
| chr6:149779536 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.192+6367G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779536 | |||||||
| chr6:149779576 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+6407G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779576 | |||||||
| chr6:149779669 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+6500G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779669 | |||||||
| chr6:149779766 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.192+6597C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149779766 | |||||||
| chr6:149780001 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.192+6832C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780001 | |||||||
| chr6:149780041 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192+6872T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780041 | |||||||
| chr6:149780211 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+7042C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780211 | |||||||
| chr6:149780508 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+7339A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780508 | |||||||
| chr6:149780563 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.192+7394T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780563 | |||||||
| chr6:149780867 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+7698G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780867 | |||||||
| chr6:149780898 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+7729A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780898 | |||||||
| chr6:149780928 | G | A | 1 | a0002c0002t0002g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.192+7759G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149780928 | |||||||
| chr6:149781191 | TTTTTTTT others(6): Show |
T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.192+8035_192+8047d others(15): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149781191 | ||||||
| chr6:149781192 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0001g0321 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.192+8035_192+8046d others(14): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149781192 | ||||||
| chr6:149781204 | G | T | 2 | a0002c0002t0003g0029 a0002c0002t0003g0030 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.192+8035G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781204 | |||||||
| chr6:149781242 | T | C | 1 | a0002c0002t0002g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.192+8073T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781242 | |||||||
| chr6:149781252 | A | T | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.192+8083A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781252 | |||||||
| chr6:149781258 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.192+8089G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781258 | |||||||
| chr6:149781361 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.192+8192G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781361 | |||||||
| chr6:149781391 | T | A | 1 | a0001c0001t0001g0316 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.192+8222T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781391 | |||||||
| chr6:149781409 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.192+8240T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781409 | |||||||
| chr6:149781442 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.192+8273G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781442 | |||||||
| chr6:149781467 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG00099.hp1 HG02080.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+8298C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781467 | |||||||
| chr6:149781556 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.192+8387A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781556 | |||||||
| chr6:149781595 | A | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0192 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-8359A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781595 | |||||||
| chr6:149781649 | A | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.193-8305A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781649 | |||||||
| chr6:149781933 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-8021A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781933 | |||||||
| chr6:149781947 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193-8007T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149781947 | |||||||
| chr6:149782138 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193-7816A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149782138 | |||||||
| chr6:149782183 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.193-7771A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149782183 | |||||||
| chr6:149782263 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.193-7691C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149782263 | |||||||
| chr6:149782617 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193-7337C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149782617 | |||||||
| chr6:149782765 | C | A | 33 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(30): Show |
33 | HG00099.hp1 HG01192.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.193-7189C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149782765 | |||||||
| chr6:149782897 | G | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-7057G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149782897 | |||||||
| chr6:149782967 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193-6987G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149782967 | |||||||
| chr6:149783009 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.193-6945A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783009 | |||||||
| chr6:149783013 | C | G | 1 | a0002c0002t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.193-6941C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783013 | |||||||
| chr6:149783124 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-6830A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783124 | |||||||
| chr6:149783199 | C | G | 4 | a0001c0001t0001g0238 a0001c0001t0001g0242 a0001c0001t0001g0277 others(1): Show |
4 | NA18964.hp2 NA18968.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-6755C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783199 | |||||||
| chr6:149783254 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.193-6700T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783254 | |||||||
| chr6:149783321 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-6633C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783321 | |||||||
| chr6:149783324 | G | C | 1 | a0002c0002t0002g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.193-6630G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783324 | |||||||
| chr6:149783335 | GT | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0206 a0001c0001t0001g0207 others(4): Show |
7 | HG01884.hp2 HG02717.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-6617delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149783335 | ||||||
| chr6:149783553 | T | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-6401T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783553 | |||||||
| chr6:149783554 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.193-6400T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783554 | |||||||
| chr6:149783578 | T | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0222 a0001c0001t0001g0321 |
3 | HG02055.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.193-6376T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783578 | |||||||
| chr6:149783578 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.193-6376T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783578 | |||||||
| chr6:149783767 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.193-6187A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783767 | |||||||
| chr6:149783940 | C | A | 3 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0286 |
3 | NA18977.hp1 NA19011.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.193-6014C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783940 | |||||||
| chr6:149783956 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-5998G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149783956 | |||||||
| chr6:149784227 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193-5727T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784227 | |||||||
| chr6:149784240 | T | C | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0215 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-5714T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784240 | |||||||
| chr6:149784244 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.193-5710C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784244 | |||||||
| chr6:149784384 | T | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-5570T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784384 | |||||||
| chr6:149784417 | A | C | 1 | a0001c0001t0001g0019 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.193-5537A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784417 | |||||||
| chr6:149784549 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-5405C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784549 | |||||||
| chr6:149784589 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.193-5365C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784589 | |||||||
| chr6:149784616 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.193-5338C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784616 | |||||||
| chr6:149784762 | T | C | 19 | a0001c0001t0001g0200 a0001c0001t0001g0204 a0001c0001t0001g0231 others(16): Show |
19 | HG00423.hp2 HG01975.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.193-5192T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784762 | |||||||
| chr6:149784836 | T | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
226 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.193-5118T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149784836 | |||||||
| chr6:149785243 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-4711T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785243 | |||||||
| chr6:149785249 | G | GTCA | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
233 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.193-4702_193-4700d others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149785249 | ||||||
| chr6:149785267 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.193-4687C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785267 | |||||||
| chr6:149785267 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-4687C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785267 | |||||||
| chr6:149785313 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.193-4641G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785313 | |||||||
| chr6:149785355 | CT | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
124 | HG00140.hp1 HG00423.hp1 HG00733.hp1 others(121): Show |
intron_variant | MODIFIER | c.193-4582delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149785355 | ||||||
| chr6:149785355 | CTT | C | 110 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(107): Show |
110 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.193-4583_193-4582d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149785355 | ||||||
| chr6:149785433 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-4521C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785433 | |||||||
| chr6:149785442 | G | T | 5 | a0002c0002t0002g0055 a0002c0002t0002g0056 a0002c0002t0002g0101 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-4512G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785442 | |||||||
| chr6:149785527 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(51): Show |
55 | HG00733.hp1 HG01192.hp2 HG02055.hp1 others(52): Show |
intron_variant | MODIFIER | c.193-4427T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785527 | |||||||
| chr6:149785545 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.193-4409G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785545 | |||||||
| chr6:149785549 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0217 |
2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.193-4405C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785549 | |||||||
| chr6:149785560 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.193-4394C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785560 | |||||||
| chr6:149785566 | G | A | 1 | a0002c0002t0002g0088 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.193-4388G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785566 | |||||||
| chr6:149785569 | T | C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-4385T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785569 | |||||||
| chr6:149785620 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.193-4334C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785620 | |||||||
| chr6:149785635 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.193-4319T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785635 | |||||||
| chr6:149785791 | T | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0240 |
2 | HG01943.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.193-4163T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785791 | |||||||
| chr6:149785860 | C | G | 1 | a0001c0001t0001g0241 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.193-4094C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785860 | |||||||
| chr6:149785883 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.193-4071C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785883 | |||||||
| chr6:149785984 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193-3970C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149785984 | |||||||
| chr6:149786005 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-3949C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786005 | |||||||
| chr6:149786014 | G | T | 1 | a0002c0002t0002g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.193-3940G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786014 | |||||||
| chr6:149786036 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.193-3918G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786036 | |||||||
| chr6:149786112 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-3842G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786112 | |||||||
| chr6:149786115 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-3839C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786115 | |||||||
| chr6:149786135 | C | G | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0215 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-3819C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786135 | |||||||
| chr6:149786140 | G | A | 3 | a0001c0001t0001g0018 a0002c0002t0002g0080 a0002c0002t0002g0108 |
3 | HG02717.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.193-3814G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786140 | |||||||
| chr6:149786156 | C | G | 1 | a0001c0001t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.193-3798C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786156 | |||||||
| chr6:149786156 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-3798C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786156 | |||||||
| chr6:149786166 | A | AC | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.193-3782dupC | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786166 | ||||||
| chr6:149786166 | A | ACC | 11 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0143 others(8): Show |
11 | HG00733.hp1 HG01109.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-3783_193-3782d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786166 | ||||||
| chr6:149786168 | CCCCCAAC others(41): Show |
C | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193-3781_193-3734d others(50): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786168 | ||||||
| chr6:149786173 | A | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-3781A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786173 | |||||||
| chr6:149786185 | A | AGACGGGG others(48): Show |
53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00733.hp1 HG02055.hp1 HG02055.hp2 others(50): Show |
intron_variant | MODIFIER | c.193-3744_193-3743i others(57): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786185 | ||||||
| chr6:149786204 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.193-3750G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786204 | |||||||
| chr6:149786205 | C | T | 4 | a0002c0002t0002g0102 a0002c0002t0002g0111 a0002c0002t0003g0029 others(1): Show |
4 | HG02698.hp1 HG03942.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-3749C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786205 | |||||||
| chr6:149786209 | G | GGTGCTGA others(48): Show |
76 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0156 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.193-3744_193-3743i others(57): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786209 | ||||||
| chr6:149786209 | G | GGTGCTGA others(48): Show |
1 | a0001c0001t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.193-3744_193-3743i others(57): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786209 | ||||||
| chr6:149786209 | G | GGTGCTGA others(48): Show |
1 | a0001c0001t0001g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.193-3744_193-3743i others(57): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786209 | ||||||
| chr6:149786209 | G | GGTGCTGA others(49): Show |
1 | a0001c0001t0001g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.193-3744_193-3743i others(58): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786209 | ||||||
| chr6:149786211 | G | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(231): Show |
235 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.193-3743G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786211 | |||||||
| chr6:149786216 | A | ACCCCCCC others(49): Show |
1 | a0001c0001t0001g0218 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.193-3720_193-3719i others(58): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786216 | ||||||
| chr6:149786216 | A | ACCCCCCC others(49): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0192 a0001c0001t0001g0194 others(2): Show |
5 | HG00423.hp1 HG00642.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-3720_193-3719i others(58): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786216 | ||||||
| chr6:149786216 | A | ACCCCCCC others(49): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0142 a0001c0001t0001g0211 |
3 | HG02280.hp1 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-3731_193-3730i others(58): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786216 | ||||||
| chr6:149786234 | C | CGGACGGG others(48): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0144 |
4 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-3720_193-3719i others(57): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786234 | |||||||
| chr6:149786235 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(231): Show |
235 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.193-3719A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786235 | |||||||
| chr6:149786239 | G | GGGACGGG others(98): Show |
7 | a0001c0001t0001g0255 a0001c0001t0001g0261 a0001c0001t0001g0266 others(4): Show |
7 | HG02523.hp1 NA18972.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-3711_193-3710i others(107): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786239 | ||||||
| chr6:149786239 | G | GGGACGGG others(99): Show |
1 | a0001c0001t0001g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.193-3711_193-3710i others(108): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786239 | ||||||
| chr6:149786243 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.193-3711C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786243 | |||||||
| chr6:149786244 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-3710A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786244 | |||||||
| chr6:149786256 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0154 |
2 | HG01109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.193-3698C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786256 | |||||||
| chr6:149786264 | G | T | 66 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0166 others(63): Show |
66 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.193-3690G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786264 | |||||||
| chr6:149786271 | A | ACCCCCCC others(49): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0143 a0001c0001t0001g0160 others(4): Show |
7 | HG01192.hp2 HG02280.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-3676_193-3675i others(58): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786271 | ||||||
| chr6:149786271 | A | ACCCCCCC others(51): Show |
1 | a0001c0001t0001g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.193-3665_193-3664i others(60): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786271 | ||||||
| chr6:149786271 | A | ACCCCCCC others(50): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0267 |
2 | HG02056.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.193-3665_193-3664i others(59): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786271 | ||||||
| chr6:149786271 | AC | A | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): Show |
69 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.193-3675delC | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786271 | ||||||
| chr6:149786272 | C | CCCCCCCA others(97): Show |
2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-3676_193-3675i others(106): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786272 | ||||||
| chr6:149786272 | C | CCCCCCCA others(98): Show |
1 | a0001c0001t0001g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.193-3676_193-3675i others(107): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786272 | ||||||
| chr6:149786288 | C | CCCGGA | 63 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0133 others(60): Show |
63 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.193-3665_193-3664i others(7): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786288 | ||||||
| chr6:149786288 | C | CCCGGACG others(54): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-3665_193-3664i others(63): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786288 | ||||||
| chr6:149786290 | A | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
168 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.193-3664A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786290 | |||||||
| chr6:149786290 | A | G | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): Show |
69 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.193-3664A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786290 | |||||||
| chr6:149786311 | C | CG | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.193-3638dupG | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786311 | ||||||
| chr6:149786315 | G | GA | 3 | a0001c0001t0001g0155 a0001c0001t0001g0311 a0001c0001t0001g0319 |
3 | HG02135.hp1 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-3639_193-3638i others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786315 | |||||||
| chr6:149786315 | G | GGT | 63 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0133 others(60): Show |
63 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.193-3638_193-3637i others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786315 | ||||||
| chr6:149786320 | A | AC | 66 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0133 others(63): Show |
66 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.193-3627dupC | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786320 | ||||||
| chr6:149786332 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.193-3622C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786332 | |||||||
| chr6:149786341 | A | G | 1 | a0002c0002t0002g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.193-3613A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786341 | |||||||
| chr6:149786347 | C | T | 5 | a0002c0002t0002g0102 a0002c0002t0002g0106 a0002c0002t0002g0107 others(2): Show |
5 | NA18944.hp1 NA18957.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-3607C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786347 | |||||||
| chr6:149786364 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.193-3590G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786364 | |||||||
| chr6:149786370 | CCCCCCCA others(40): Show |
C | 9 | a0002c0002t0002g0042 a0002c0002t0002g0073 a0002c0002t0002g0074 others(6): Show |
9 | HG02698.hp1 HG03490.hp2 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-3552_193-3506d others(49): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786370 | ||||||
| chr6:149786396 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-3558T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786396 | |||||||
| chr6:149786408 | C | CG | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
176 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.193-3541dupG | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786408 | ||||||
| chr6:149786417 | A | AC | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
176 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.193-3531dupC | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786417 | ||||||
| chr6:149786434 | C | T | 59 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0198 others(56): Show |
59 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.193-3520C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786434 | |||||||
| chr6:149786438 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(50): Show |
54 | HG00733.hp1 HG01192.hp2 HG02055.hp1 others(51): Show |
intron_variant | MODIFIER | c.193-3516C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786438 | |||||||
| chr6:149786443 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
174 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.193-3511T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786443 | |||||||
| chr6:149786447 | T | TG | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3506dupG | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786447 | ||||||
| chr6:149786450 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-3504T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786450 | |||||||
| chr6:149786450 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193-3504T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786450 | |||||||
| chr6:149786451 | G | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-3503G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786451 | |||||||
| chr6:149786457 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3497A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786457 | |||||||
| chr6:149786459 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3495A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786459 | |||||||
| chr6:149786459 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-3495A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786459 | |||||||
| chr6:149786460 | C | CTG | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-3494_193-3493i others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786460 | |||||||
| chr6:149786461 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-3493G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786461 | |||||||
| chr6:149786461 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3493G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786461 | |||||||
| chr6:149786463 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3491T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786463 | |||||||
| chr6:149786463 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-3491T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786463 | |||||||
| chr6:149786466 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-3488T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786466 | |||||||
| chr6:149786470 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3484T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786470 | |||||||
| chr6:149786474 | C | CTCCT | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-3480_193-3479i others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786474 | |||||||
| chr6:149786475 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3479A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786475 | |||||||
| chr6:149786478 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3476C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786478 | |||||||
| chr6:149786483 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3471T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786483 | |||||||
| chr6:149786490 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.193-3464C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786490 | |||||||
| chr6:149786491 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.193-3463A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786491 | |||||||
| chr6:149786497 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3457A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786497 | |||||||
| chr6:149786499 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3455G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786499 | |||||||
| chr6:149786500 | G | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3454G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786500 | |||||||
| chr6:149786501 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3453G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786501 | |||||||
| chr6:149786503 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3451T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786503 | |||||||
| chr6:149786506 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3448T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786506 | |||||||
| chr6:149786510 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3444T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786510 | |||||||
| chr6:149786513 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.193-3441T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786513 | |||||||
| chr6:149786515 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3439A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786515 | |||||||
| chr6:149786523 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.193-3431C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786523 | |||||||
| chr6:149786531 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3423G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786531 | |||||||
| chr6:149786539 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3415G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786539 | |||||||
| chr6:149786540 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3414G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786540 | |||||||
| chr6:149786541 | GCTCCTCA others(33): Show |
G | 58 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0198 others(55): Show |
58 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.193-3396_193-3357d others(42): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786541 | ||||||
| chr6:149786553 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3401T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786553 | |||||||
| chr6:149786563 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3391C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786563 | |||||||
| chr6:149786564 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(47): Show |
50 | HG00423.hp1 HG00735.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.193-3390G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786564 | |||||||
| chr6:149786566 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.193-3388T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786566 | |||||||
| chr6:149786571 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-3383A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786571 | |||||||
| chr6:149786575 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.193-3379A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786575 | |||||||
| chr6:149786581 | T | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.193-3373T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786581 | |||||||
| chr6:149786598 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3356T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786598 | |||||||
| chr6:149786612 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3342A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786612 | |||||||
| chr6:149786616 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3338A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786616 | |||||||
| chr6:149786617 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-3337C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786617 | |||||||
| chr6:149786648 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.193-3306G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786648 | |||||||
| chr6:149786657 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.193-3297C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786657 | |||||||
| chr6:149786660 | T | C | 1 | a0002c0002t0002g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.193-3294T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786660 | |||||||
| chr6:149786664 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-3290C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786664 | |||||||
| chr6:149786675 | C | G | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.193-3279C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786675 | |||||||
| chr6:149786685 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.193-3269G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786685 | |||||||
| chr6:149786687 | C | T | 108 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(105): Show |
108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.193-3267C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786687 | |||||||
| chr6:149786715 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193-3239C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786715 | |||||||
| chr6:149786778 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-3176C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786778 | |||||||
| chr6:149786799 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.193-3155T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786799 | |||||||
| chr6:149786806 | A | G | 1 | a0002c0002t0002g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.193-3148A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786806 | |||||||
| chr6:149786843 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.193-3111T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786843 | |||||||
| chr6:149786859 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.193-3095T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786859 | |||||||
| chr6:149786862 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.193-3092T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786862 | |||||||
| chr6:149786863 | A | T | 1 | a0002c0002t0002g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.193-3091A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786863 | |||||||
| chr6:149786871 | C | CG | 5 | a0001c0001t0001g0122 a0001c0001t0001g0237 a0001c0001t0001g0269 others(2): Show |
5 | HG02071.hp2 HG02145.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-3079dupG | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149786871 | ||||||
| chr6:149786902 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.193-3052C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786902 | |||||||
| chr6:149786963 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.193-2991C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149786963 | |||||||
| chr6:149787005 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-2949G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787005 | |||||||
| chr6:149787138 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-2816T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787138 | |||||||
| chr6:149787152 | CCTGCAAT others(5): Show |
C | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.193-2801_193-2790d others(14): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787152 | |||||||
| chr6:149787170 | C | T | 1 | a0002c0002t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.193-2784C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787170 | |||||||
| chr6:149787171 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-2783G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787171 | |||||||
| chr6:149787182 | G | A | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0215 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-2772G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787182 | |||||||
| chr6:149787224 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-2730G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787224 | |||||||
| chr6:149787271 | A | AGAGAGGG others(10): Show |
154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(151): Show |
154 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.193-2682_193-2666d others(19): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149787271 | ||||||
| chr6:149787271 | A | AGAGAGGG others(27): Show |
1 | a0001c0001t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.193-2666_193-2665i others(36): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149787271 | ||||||
| chr6:149787272 | GAGAGGGA others(10): Show |
G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193-2665_193-2649d others(19): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149787272 | ||||||
| chr6:149787289 | T | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-2665T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787289 | |||||||
| chr6:149787369 | A | AT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(13): Show |
17 | HG00733.hp1 HG01243.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.193-2570dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149787369 | ||||||
| chr6:149787383 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.193-2571T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787383 | |||||||
| chr6:149787414 | T | C | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-2540T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787414 | |||||||
| chr6:149787427 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.193-2527C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787427 | |||||||
| chr6:149787473 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
7 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-2481T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787473 | |||||||
| chr6:149787615 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-2339G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787615 | |||||||
| chr6:149787626 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193-2328G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787626 | |||||||
| chr6:149787692 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.193-2262C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787692 | |||||||
| chr6:149787742 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193-2212C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787742 | |||||||
| chr6:149787823 | CTG | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
228 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.193-2111_193-2110d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149787823 | ||||||
| chr6:149787920 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-2034C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787920 | |||||||
| chr6:149787970 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-1984T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149787970 | |||||||
| chr6:149788022 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.193-1932A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788022 | |||||||
| chr6:149788062 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.193-1892C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788062 | |||||||
| chr6:149788074 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-1880C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788074 | |||||||
| chr6:149788159 | C | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
226 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.193-1795C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788159 | |||||||
| chr6:149788193 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.193-1761G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788193 | |||||||
| chr6:149788246 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.193-1708C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788246 | |||||||
| chr6:149788338 | A | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-1616A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788338 | |||||||
| chr6:149788477 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-1477A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788477 | |||||||
| chr6:149788479 | T | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-1475T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788479 | |||||||
| chr6:149788498 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.193-1456T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788498 | |||||||
| chr6:149788544 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.193-1410C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788544 | |||||||
| chr6:149788618 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.193-1336G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788618 | |||||||
| chr6:149788640 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-1314G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788640 | |||||||
| chr6:149788709 | C | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-1245C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788709 | |||||||
| chr6:149788941 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-1013G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788941 | |||||||
| chr6:149788973 | G | A | 2 | a0002c0002t0002g0053 a0002c0002t0002g0064 |
2 | NA18966.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.193-981G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788973 | |||||||
| chr6:149788977 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.193-977G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149788977 | |||||||
| chr6:149789066 | A | AT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
14 | HG02027.hp2 HG02080.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.193-863dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149789066 | ||||||
| chr6:149789066 | AT | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
77 | HG00099.hp2 HG00423.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.193-863delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149789066 | ||||||
| chr6:149789066 | ATT | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0156 others(139): Show |
142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.193-864_193-863del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149789066 | ||||||
| chr6:149789066 | ATTT | A | 8 | a0001c0001t0001g0161 a0001c0001t0001g0180 a0001c0001t0001g0203 others(5): Show |
8 | HG01516.hp2 HG02155.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-865_193-863del others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149789066 | ||||||
| chr6:149789068 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-886T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789068 | |||||||
| chr6:149789069 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.193-885T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789069 | |||||||
| chr6:149789080 | T | A | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193-874T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789080 | |||||||
| chr6:149789170 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.193-784G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789170 | |||||||
| chr6:149789312 | G | C | 2 | a0002c0002t0002g0065 a0002c0002t0002g0069 |
2 | HG00280.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.193-642G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789312 | |||||||
| chr6:149789320 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.193-634C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789320 | |||||||
| chr6:149789350 | T | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.193-604T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789350 | |||||||
| chr6:149789360 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0144 |
4 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-594G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789360 | |||||||
| chr6:149789420 | G | A | 1 | a0001c0001t0009g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.193-534G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789420 | |||||||
| chr6:149789464 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193-490G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789464 | |||||||
| chr6:149789486 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.193-468C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789486 | |||||||
| chr6:149789721 | TAA | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.193-230_193-229del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149789721 | ||||||
| chr6:149789760 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.193-194T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789760 | |||||||
| chr6:149789778 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193-176T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 3/7 | chr6 | 149789778 | |||||||
| chr6:149790229 | C | A | 1 | a0002c0002t0002g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.297+171C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790229 | |||||||
| chr6:149790298 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.297+240C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790298 | |||||||
| chr6:149790351 | G | T | 1 | a0002c0002t0002g0101 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.297+293G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790351 | |||||||
| chr6:149790510 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.297+452T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790510 | |||||||
| chr6:149790516 | C | CT | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.297+474dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 149790516 | ||||||
| chr6:149790516 | C | CTT | 9 | a0001c0001t0001g0138 a0001c0001t0001g0155 a0001c0001t0001g0230 others(6): Show |
9 | HG01884.hp2 HG02027.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+473_297+474dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 149790516 | ||||||
| chr6:149790520 | T | TC | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+462_297+463ins others(1): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790520 | |||||||
| chr6:149790539 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.297+481A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790539 | |||||||
| chr6:149790807 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.297+749G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790807 | |||||||
| chr6:149790830 | G | A | 1 | a0002c0002t0002g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.297+772G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149790830 | |||||||
| chr6:149791033 | C | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.297+975C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791033 | |||||||
| chr6:149791063 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.297+1005C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791063 | |||||||
| chr6:149791065 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.297+1007G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791065 | |||||||
| chr6:149791193 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.297+1135G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791193 | |||||||
| chr6:149791380 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.297+1322G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791380 | |||||||
| chr6:149791392 | A | G | 11 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0215 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+1334A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791392 | |||||||
| chr6:149791811 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.298-1738A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791811 | |||||||
| chr6:149791860 | T | C | 1 | a0002c0002t0002g0082 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.298-1689T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791860 | |||||||
| chr6:149791861 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.298-1688G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791861 | |||||||
| chr6:149791937 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.298-1612C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149791937 | |||||||
| chr6:149791954 | A | AC | 7 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0141 others(4): Show |
7 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-1591dupC | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 149791954 | ||||||
| chr6:149792036 | C | T | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(25): Show |
28 | HG00099.hp1 HG01192.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-1513C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792036 | |||||||
| chr6:149792332 | C | T | 30 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0163 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.298-1217C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792332 | |||||||
| chr6:149792357 | T | C | 8 | a0002c0002t0002g0036 a0002c0002t0002g0044 a0002c0002t0002g0047 others(5): Show |
8 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-1192T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792357 | |||||||
| chr6:149792575 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.298-974C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792575 | |||||||
| chr6:149792658 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.298-891G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792658 | |||||||
| chr6:149792666 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.298-883T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792666 | |||||||
| chr6:149792971 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298-578A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792971 | |||||||
| chr6:149792990 | G | A | 17 | a0001c0001t0001g0172 a0002c0002t0002g0024 a0002c0002t0002g0025 others(14): Show |
17 | HG00323.hp2 HG00733.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.298-559G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149792990 | |||||||
| chr6:149793162 | CAA | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.298-373_298-372del others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 149793162 | ||||||
| chr6:149793163 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.298-386A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149793163 | |||||||
| chr6:149793163 | A | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02895.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.298-386A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149793163 | |||||||
| chr6:149793164 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02895.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.298-385A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149793164 | |||||||
| chr6:149793195 | A | C | 6 | a0001c0001t0001g0198 a0001c0001t0001g0253 a0001c0001t0001g0281 others(3): Show |
6 | HG01433.hp2 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-354A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149793195 | |||||||
| chr6:149793280 | G | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0291 |
3 | HG03927.hp2 NA18747.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.298-269G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149793280 | |||||||
| chr6:149793470 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.298-79C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 4/7 | chr6 | 149793470 | |||||||
| chr6:149793871 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.418+202C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149793871 | |||||||
| chr6:149793947 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+278G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149793947 | |||||||
| chr6:149793993 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.418+324T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149793993 | |||||||
| chr6:149794085 | A | C | 1 | a0001c0001t0001g0307 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.418+416A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794085 | |||||||
| chr6:149794100 | C | T | 1 | a0002c0002t0002g0060 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.418+431C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794100 | |||||||
| chr6:149794147 | A | G | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.418+478A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794147 | |||||||
| chr6:149794149 | C | G | 1 | a0002c0002t0002g0057 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.418+480C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794149 | |||||||
| chr6:149794263 | G | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0249 a0001c0001t0001g0288 |
3 | HG03017.hp2 HG04199.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.418+594G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794263 | |||||||
| chr6:149794332 | A | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.418+663A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794332 | |||||||
| chr6:149794378 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.418+709G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794378 | |||||||
| chr6:149794483 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+814T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794483 | |||||||
| chr6:149794495 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.418+826G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794495 | |||||||
| chr6:149794505 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.418+836C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794505 | |||||||
| chr6:149794670 | AT | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.418+1002delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794670 | |||||||
| chr6:149794671 | T | C | 93 | a0002c0002t0002g0001 a0002c0002t0002g0024 a0002c0002t0002g0025 others(90): Show |
94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.418+1002T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794671 | |||||||
| chr6:149794675 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.418+1006C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149794675 | |||||||
| chr6:149795108 | G | A | 1 | a0001c0001t0009g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.419-1307G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795108 | |||||||
| chr6:149795149 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-1266C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795149 | |||||||
| chr6:149795193 | CA | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.419-1208delA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 149795193 | ||||||
| chr6:149795229 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.419-1186C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795229 | |||||||
| chr6:149795271 | C | T | 1 | a0002c0002t0002g0040 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.419-1144C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795271 | |||||||
| chr6:149795289 | T | C | 2 | a0002c0002t0002g0101 a0002c0002t0002g0113 |
2 | HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.419-1126T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795289 | |||||||
| chr6:149795298 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.419-1117G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795298 | |||||||
| chr6:149795484 | T | G | 1 | a0001c0001t0001g0322 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.419-931T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795484 | |||||||
| chr6:149795490 | C | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.419-925C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795490 | |||||||
| chr6:149795662 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.419-753C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795662 | |||||||
| chr6:149795772 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.419-643T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795772 | |||||||
| chr6:149795775 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0241 |
2 | HG02074.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.419-640G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795775 | |||||||
| chr6:149795901 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0209 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.419-514G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795901 | |||||||
| chr6:149795919 | T | G | 2 | a0002c0002t0002g0102 a0002c0002t0002g0111 |
2 | NA18962.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.419-496T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795919 | |||||||
| chr6:149795984 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.419-431C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795984 | |||||||
| chr6:149795997 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.419-418C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149795997 | |||||||
| chr6:149796013 | A | G | 1 | a0002c0002t0002g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.419-402A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 5/7 | chr6 | 149796013 | |||||||
| chr6:149796760 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+260C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149796760 | |||||||
| chr6:149796792 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.504+292T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149796792 | |||||||
| chr6:149796818 | G | GT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0119 others(6): Show |
10 | HG02886.hp2 HG02922.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.504+324dupT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 149796818 | ||||||
| chr6:149796825 | G | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.504+325G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149796825 | |||||||
| chr6:149796906 | C | T | 1 | a0002c0002t0002g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.504+406C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149796906 | |||||||
| chr6:149796930 | T | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.504+430T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149796930 | |||||||
| chr6:149796958 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+458C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149796958 | |||||||
| chr6:149797084 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.504+584G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797084 | |||||||
| chr6:149797145 | A | G | 1 | a0002c0002t0002g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.504+645A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797145 | |||||||
| chr6:149797172 | T | C | 1 | a0001c0001t0009g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.504+672T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797172 | |||||||
| chr6:149797172 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+672T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797172 | |||||||
| chr6:149797183 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.504+683T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797183 | |||||||
| chr6:149797188 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+688A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797188 | |||||||
| chr6:149797323 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.504+823A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797323 | |||||||
| chr6:149797513 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.504+1013T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797513 | |||||||
| chr6:149797517 | T | TA | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.504+1027dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 149797517 | ||||||
| chr6:149797531 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.504+1031G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797531 | |||||||
| chr6:149797621 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.504+1121T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797621 | |||||||
| chr6:149797641 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.504+1141G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797641 | |||||||
| chr6:149797707 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.504+1207C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797707 | |||||||
| chr6:149797750 | G | A | 2 | a0002c0002t0002g0047 a0002c0002t0002g0085 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.504+1250G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797750 | |||||||
| chr6:149797913 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+1413C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797913 | |||||||
| chr6:149797947 | C | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0308 |
2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.504+1447C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797947 | |||||||
| chr6:149797953 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.504+1453C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797953 | |||||||
| chr6:149797981 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.504+1481C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149797981 | |||||||
| chr6:149798164 | GTC | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.504+1667_504+1668d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 149798164 | ||||||
| chr6:149798166 | CT | C | 13 | a0001c0001t0001g0187 a0001c0001t0001g0192 a0001c0001t0001g0209 others(10): Show |
13 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+1667delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798166 | |||||||
| chr6:149798168 | C | A | 13 | a0001c0001t0001g0187 a0001c0001t0001g0192 a0001c0001t0001g0209 others(10): Show |
13 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+1668C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798168 | |||||||
| chr6:149798169 | A | C | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.504+1669A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798169 | |||||||
| chr6:149798205 | T | TA | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.504+1706dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 149798205 | ||||||
| chr6:149798260 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.504+1760G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798260 | |||||||
| chr6:149798294 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.504+1794G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798294 | |||||||
| chr6:149798308 | C | A | 1 | a0002c0002t0002g0332 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.504+1808C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798308 | |||||||
| chr6:149798630 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.504+2130A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798630 | |||||||
| chr6:149798687 | C | A | 1 | a0001c0001t0009g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.504+2187C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798687 | |||||||
| chr6:149798723 | A | G | 2 | a0002c0002t0002g0024 a0002c0002t0002g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.504+2223A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798723 | |||||||
| chr6:149798774 | A | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.504+2274A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798774 | |||||||
| chr6:149798827 | C | G | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+2327C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798827 | |||||||
| chr6:149798900 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.504+2400T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798900 | |||||||
| chr6:149798951 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+2451A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798951 | |||||||
| chr6:149798979 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18969.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.504+2479A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149798979 | |||||||
| chr6:149799051 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.504+2551C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799051 | |||||||
| chr6:149799093 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.504+2593G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799093 | |||||||
| chr6:149799133 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0229 |
2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.504+2633C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799133 | |||||||
| chr6:149799322 | AT | A | 27 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(24): Show |
27 | HG00099.hp1 HG01192.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.504+2823delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799322 | |||||||
| chr6:149799444 | A | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.505-2756A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799444 | |||||||
| chr6:149799638 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0196 |
2 | HG00558.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.505-2562C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799638 | |||||||
| chr6:149799677 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.505-2523A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799677 | |||||||
| chr6:149799964 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.505-2236C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149799964 | |||||||
| chr6:149800418 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.505-1782G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149800418 | |||||||
| chr6:149800506 | CA | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-1688delA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 149800506 | ||||||
| chr6:149800557 | C | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.505-1643C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149800557 | |||||||
| chr6:149800561 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.505-1639A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149800561 | |||||||
| chr6:149800854 | C | G | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.505-1346C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149800854 | |||||||
| chr6:149800860 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | NA18963.hp1 NA19002.hp2 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-1340C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149800860 | |||||||
| chr6:149800957 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.505-1243C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149800957 | |||||||
| chr6:149801042 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.505-1158C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801042 | |||||||
| chr6:149801234 | T | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0222 a0001c0001t0001g0321 |
3 | HG02055.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.505-966T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801234 | |||||||
| chr6:149801253 | C | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.505-947C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801253 | |||||||
| chr6:149801268 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.505-932T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801268 | |||||||
| chr6:149801273 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.505-927T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801273 | |||||||
| chr6:149801509 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.505-691G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801509 | |||||||
| chr6:149801926 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.505-274C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801926 | |||||||
| chr6:149801984 | C | G | 1 | a0001c0001t0001g0003 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.505-216C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | chr6 | 149801984 | |||||||
| chr6:149802180 | CT | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
splice_region_variant&intron_variant | LOW | c.505-8delT | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 149802180 | ||||||
| chr6:149802504 | T | C | 5 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0262 others(2): Show |
5 | HG00735.hp2 HG01074.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.*37+88T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802504 | |||||||
| chr6:149802615 | G | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*37+199G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802615 | |||||||
| chr6:149802618 | T | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*37+202T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802618 | |||||||
| chr6:149802619 | G | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*37+203G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802619 | |||||||
| chr6:149802627 | G | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.*37+211G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802627 | |||||||
| chr6:149802628 | T | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.*37+212T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802628 | |||||||
| chr6:149802633 | T | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0238 a0001c0001t0001g0245 |
3 | HG00639.hp1 NA18982.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.*37+217T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802633 | |||||||
| chr6:149802882 | C | T | 12 | a0002c0002t0002g0089 a0002c0002t0002g0090 a0002c0002t0002g0091 others(9): Show |
12 | HG01358.hp1 HG02040.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.*37+466C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802882 | |||||||
| chr6:149802883 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*37+467G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149802883 | |||||||
| chr6:149803052 | C | CA | 31 | a0002c0002t0002g0025 a0002c0002t0002g0035 a0002c0002t0002g0044 others(28): Show |
31 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.*37+666dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803052 | ||||||
| chr6:149803052 | C | CAA | 12 | a0002c0002t0002g0024 a0002c0002t0002g0026 a0002c0002t0002g0032 others(9): Show |
12 | HG01243.hp2 HG01261.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.*37+665_*37+666dup others(2): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803052 | ||||||
| chr6:149803052 | C | CAAA | 6 | a0002c0002t0002g0031 a0002c0002t0002g0038 a0002c0002t0002g0047 others(3): Show |
6 | HG00140.hp1 HG00323.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.*37+664_*37+666dup others(3): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803052 | ||||||
| chr6:149803052 | CAAAAAA | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0125 a0001c0001t0001g0135 others(16): Show |
19 | HG00140.hp2 HG00735.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.*37+661_*37+666del others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803052 | ||||||
| chr6:149803052 | CAAAAAAA | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.*37+660_*37+666del others(7): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803052 | ||||||
| chr6:149803052 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*37+656_*37+666del others(11): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803052 | ||||||
| chr6:149803071 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02895.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.*37+655A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803071 | |||||||
| chr6:149803075 | A | C | 1 | a0002c0002t0002g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.*37+659A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803075 | |||||||
| chr6:149803077 | A | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.*37+661A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803077 | |||||||
| chr6:149803100 | C | T | 2 | a0002c0002t0002g0048 a0002c0002t0002g0049 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.*37+684C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803100 | |||||||
| chr6:149803147 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*37+731G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803147 | |||||||
| chr6:149803280 | C | G | 2 | a0002c0002t0002g0047 a0002c0002t0002g0085 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.*37+864C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803280 | |||||||
| chr6:149803297 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.*37+881A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803297 | |||||||
| chr6:149803400 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*37+984C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803400 | |||||||
| chr6:149803478 | C | CATAATCT others(298): Show |
1 | a0001c0001t0001g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.*37+1078_*37+1079i others(307): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803478 | ||||||
| chr6:149803478 | C | CATAATCT others(299): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0246 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.*37+1078_*37+1079i others(308): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803478 | ||||||
| chr6:149803509 | T | TTTCTC | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*37+1096_*37+1100d others(7): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803509 | ||||||
| chr6:149803641 | A | G | 1 | a0002c0002t0002g0076 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.*37+1225A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149803641 | |||||||
| chr6:149803797 | GA | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.*37+1401delA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803797 | ||||||
| chr6:149803797 | GAA | G | 15 | a0001c0001t0001g0018 a0001c0001t0001g0133 a0001c0001t0001g0135 others(12): Show |
15 | HG01109.hp1 HG02717.hp2 HG03209.hp1 others(12): Show |
intron_variant | MODIFIER | c.*37+1400_*37+1401d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149803797 | ||||||
| chr6:149804080 | C | CA | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.*37+1687dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149804080 | ||||||
| chr6:149804080 | C | CAA | 37 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0019 others(34): Show |
38 | HG00733.hp1 HG01109.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.*37+1686_*37+1687d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149804080 | ||||||
| chr6:149804154 | A | G | 2 | a0002c0002t0002g0101 a0002c0002t0002g0113 |
2 | HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.*37+1738A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149804154 | |||||||
| chr6:149804456 | G | T | 9 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.*37+2040G>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149804456 | |||||||
| chr6:149804483 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*37+2067T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149804483 | |||||||
| chr6:149804722 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0217 |
2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.*37+2306G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149804722 | |||||||
| chr6:149804753 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.*37+2337C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149804753 | |||||||
| chr6:149804795 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*37+2379C>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149804795 | |||||||
| chr6:149804804 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*37+2388G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149804804 | |||||||
| chr6:149805116 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*37+2700C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805116 | |||||||
| chr6:149805133 | T | C | 3 | a0002c0002t0002g0043 a0002c0002t0002g0053 a0002c0002t0002g0064 |
3 | NA18966.hp1 NA18968.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.*37+2717T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805133 | |||||||
| chr6:149805315 | T | C | 5 | a0001c0001t0001g0154 a0001c0001t0001g0220 a0001c0001t0001g0249 others(2): Show |
5 | HG00733.hp2 HG01109.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.*37+2899T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805315 | |||||||
| chr6:149805319 | C | T | 50 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0198 others(47): Show |
50 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.*37+2903C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805319 | |||||||
| chr6:149805320 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*37+2904G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805320 | |||||||
| chr6:149805321 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*37+2905C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805321 | |||||||
| chr6:149805322 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0304 |
2 | HG01109.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.*37+2906A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805322 | |||||||
| chr6:149805409 | T | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0319 a0002c0002t0002g0082 |
3 | HG03225.hp2 HG03516.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.*37+2993T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805409 | |||||||
| chr6:149805410 | G | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0319 a0002c0002t0002g0082 |
3 | HG03225.hp2 HG03516.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.*37+2994G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805410 | |||||||
| chr6:149805412 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0319 a0002c0002t0002g0082 |
3 | HG03225.hp2 HG03516.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.*37+2996C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805412 | |||||||
| chr6:149805549 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*37+3133G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805549 | |||||||
| chr6:149805555 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.*37+3139T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805555 | |||||||
| chr6:149805588 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.*37+3172C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805588 | |||||||
| chr6:149805589 | G | A | 1 | a0002c0002t0002g0114 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.*37+3173G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805589 | |||||||
| chr6:149805739 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*37+3323C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805739 | |||||||
| chr6:149805748 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*37+3332C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805748 | |||||||
| chr6:149805930 | ACT | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.*37+3517_*37+3518d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149805930 | ||||||
| chr6:149805939 | CA | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
84 | HG00423.hp1 HG00733.hp1 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.*37+3541delA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149805939 | ||||||
| chr6:149805939 | CAA | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0138 a0001c0001t0001g0144 others(5): Show |
8 | HG01884.hp2 HG02523.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.*37+3540_*37+3541d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149805939 | ||||||
| chr6:149805939 | CAAAA | C | 22 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0115 others(19): Show |
22 | HG00099.hp1 HG01192.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.*37+3538_*37+3541d others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149805939 | ||||||
| chr6:149805967 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*37+3551C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149805967 | |||||||
| chr6:149806113 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.*37+3697C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806113 | |||||||
| chr6:149806223 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0023 |
2 | HG02080.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.*37+3807G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806223 | |||||||
| chr6:149806304 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.*37+3888G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806304 | |||||||
| chr6:149806357 | G | C | 4 | a0002c0002t0002g0089 a0002c0002t0002g0090 a0002c0002t0002g0091 others(1): Show |
4 | NA18960.hp1 NA18980.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37+3941G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806357 | |||||||
| chr6:149806374 | G | A | 10 | a0002c0002t0002g0054 a0002c0002t0002g0057 a0002c0002t0002g0058 others(7): Show |
10 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.*37+3958G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806374 | |||||||
| chr6:149806474 | A | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0258 a0001c0001t0001g0260 others(1): Show |
4 | HG01952.hp2 HG02004.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37+4058A>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806474 | |||||||
| chr6:149806579 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*38-4037G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806579 | |||||||
| chr6:149806585 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*38-4031G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806585 | |||||||
| chr6:149806727 | A | C | 3 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0035 |
4 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.*38-3889A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806727 | |||||||
| chr6:149806747 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.*38-3869A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806747 | |||||||
| chr6:149806751 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*38-3865A>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806751 | |||||||
| chr6:149806812 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*38-3804G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806812 | |||||||
| chr6:149806872 | T | G | 1 | a0002c0002t0002g0078 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.*38-3744T>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149806872 | |||||||
| chr6:149807037 | C | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*38-3579C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149807037 | |||||||
| chr6:149807296 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.*38-3320G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149807296 | |||||||
| chr6:149807495 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0330 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.*38-3121C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149807495 | |||||||
| chr6:149807511 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*38-3105C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149807511 | |||||||
| chr6:149807524 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*38-3092C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149807524 | |||||||
| chr6:149807529 | C | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.*38-3087C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149807529 | |||||||
| chr6:149808187 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.*38-2429A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808187 | |||||||
| chr6:149808223 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.*38-2393G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808223 | |||||||
| chr6:149808434 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*38-2182C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808434 | |||||||
| chr6:149808436 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*38-2180C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808436 | |||||||
| chr6:149808470 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*38-2146T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808470 | |||||||
| chr6:149808473 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*38-2143A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808473 | |||||||
| chr6:149808497 | C | A | 1 | a0002c0002t0002g0025 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.*38-2119C>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808497 | |||||||
| chr6:149808519 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*38-2097A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808519 | |||||||
| chr6:149808752 | T | A | 1 | a0001c0001t0001g0241 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.*38-1864T>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808752 | |||||||
| chr6:149808798 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*38-1818G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808798 | |||||||
| chr6:149808843 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*38-1773A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808843 | |||||||
| chr6:149808883 | G | A | 1 | a0002c0002t0002g0096 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.*38-1733G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808883 | |||||||
| chr6:149808887 | T | C | 1 | a0002c0002t0002g0096 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.*38-1729T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808887 | |||||||
| chr6:149808971 | T | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.*38-1645T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149808971 | |||||||
| chr6:149809052 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*38-1564C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809052 | |||||||
| chr6:149809054 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*38-1562A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809054 | |||||||
| chr6:149809118 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*38-1498G>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809118 | |||||||
| chr6:149809191 | A | G | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.*38-1425A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809191 | |||||||
| chr6:149809258 | C | CA | 12 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0216 others(9): Show |
12 | HG01255.hp1 HG02004.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.*38-1335dupA | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149809258 | ||||||
| chr6:149809258 | C | CAA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0135 a0001c0001t0001g0155 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.*38-1336_*38-1335d others(4): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149809258 | ||||||
| chr6:149809258 | C | CAAA | 43 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(40): Show |
44 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.*38-1337_*38-1335d others(5): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149809258 | ||||||
| chr6:149809258 | C | CAAAA | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.*38-1338_*38-1335d others(6): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149809258 | ||||||
| chr6:149809258 | C | CAAAAA | 45 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(42): Show |
45 | HG00423.hp1 HG00423.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.*38-1339_*38-1335d others(7): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149809258 | ||||||
| chr6:149809300 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0319 a0001c0001t0001g0320 |
3 | HG02976.hp1 HG03516.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.*38-1316A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809300 | |||||||
| chr6:149809506 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.*38-1110C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809506 | |||||||
| chr6:149809537 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*38-1079G>A | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809537 | |||||||
| chr6:149809701 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*38-915A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809701 | |||||||
| chr6:149809757 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.*38-859A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149809757 | |||||||
| chr6:149810072 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.*38-544T>C | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149810072 | |||||||
| chr6:149810392 | C | T | 1 | a0002c0002t0002g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.*38-224C>T | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149810392 | |||||||
| chr6:149810546 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*38-70A>G | PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 7/7 | chr6 | 149810546 |