Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283209 |
| ensemblid | ENSG00000165434.8 |
| hgncid | 20898 |
| symbol | PGM2L1 |
| name | phosphoglucomutase 2 like 1 |
| refseq_nuc | NM_173582.6 |
| refseq_prot | NP_775853.2 |
| ensembl_nuc | ENST00000298198.5 |
| ensembl_prot | ENSP00000298198.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 74330316 |
| end | 74398433 |
| strand | - |
| ver | v1.2 |
| region | chr11:74330316-74398433 |
| region5000 | chr11:74325316-74403433 |
| regionname0 | PGM2L1_chr11_74330316_74398433 |
| regionname5000 | PGM2L1_chr11_74325316_74403433 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 622 | 182 | 63 | 26 | 67 | 6 | 19 | 51 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0002 | 1/0 | 622 | 94 | 19 | 13 | 50 | 3 | 8 | 43 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0003 | 0/0 | 622 | 89 | 8 | 7 | 63 | 3 | 8 | 46 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0004 | 0/0 | 622 | 7 | 1 | 2 | 0 | 0 | 4 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0005 | 0/0 | 622 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0006 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0007 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0008 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0009 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| a0010 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | MAENT others(617): Show |
chr11 | 74325316 | 74403433 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1866 | 123 | 16 | 21 | 62 | 6 | 17 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0001c0004 | 0/0 | 1866 | 57 | 45 | 5 | 5 | 0 | 2 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0001c0009 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0001c0013 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0002c0002 | 1/0 | 1866 | 94 | 19 | 13 | 50 | 3 | 8 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0003c0003 | 0/0 | 1866 | 86 | 5 | 7 | 63 | 3 | 8 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0003c0006 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0004c0005 | 0/0 | 1866 | 7 | 1 | 2 | 0 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0005c0007 | 0/0 | 1866 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0006c0012 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0007c0010 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0008c0014 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0009c0011 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 | ||
| a0010c0008 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATGGC others(1861): Show |
chr11 | 74325316 | 74403433 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8481 | 52 | 1 | 6 | 41 | 1 | 3 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0002 | 0/0 | 8479 | 7 | 3 | 1 | 1 | 0 | 2 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8474): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0003 | 0/0 | 8481 | 45 | 5 | 12 | 16 | 3 | 9 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0011 | 0/0 | 8482 | 4 | 1 | 1 | 0 | 2 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8477): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0020 | 0/0 | 8482 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8477): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0022 | 0/0 | 8474 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8469): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0030 | 0/1 | 8481 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0033 | 0/0 | 8481 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0034 | 0/0 | 8481 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0035 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0036 | 0/0 | 8477 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0037 | 0/0 | 8481 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0039 | 0/0 | 8480 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8475): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0041 | 0/0 | 8475 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8470): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0043 | 0/0 | 8479 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8474): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0044 | 0/0 | 8475 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8470): Show |
chr11 | 74325316 | 74403433 |
| a0001c0001t0045 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0008 | 0/0 | 8476 | 11 | 11 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0009 | 0/0 | 8474 | 9 | 9 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8469): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0010 | 0/0 | 8477 | 8 | 1 | 1 | 5 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0013 | 0/0 | 8476 | 4 | 4 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0015 | 0/0 | 8476 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0016 | 0/0 | 8476 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0017 | 0/0 | 8477 | 4 | 3 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0019 | 0/0 | 8475 | 3 | 2 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8470): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0023 | 0/0 | 8476 | 2 | 1 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0024 | 0/0 | 8475 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8470): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0025 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0026 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0029 | 0/0 | 8477 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0046 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0049 | 0/0 | 8481 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0058 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0059 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0001c0004t0060 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0009t0029 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0001c0013t0032 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0004 | 0/0 | 8477 | 44 | 19 | 3 | 16 | 2 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0005 | 1/0 | 8477 | 40 | 0 | 8 | 27 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0027 | 0/0 | 8477 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0028 | 0/0 | 8476 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0051 | 0/0 | 8477 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0052 | 0/0 | 8477 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0053 | 0/0 | 8476 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0054 | 0/0 | 8477 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0056 | 0/0 | 8477 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0002c0002t0057 | 0/0 | 8476 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0001 | 0/0 | 8481 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0002 | 0/0 | 8479 | 42 | 4 | 3 | 29 | 3 | 3 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8474): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0003 | 0/0 | 8481 | 2 | 0 | 0 | 0 | 0 | 2 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0006 | 0/0 | 8479 | 13 | 0 | 2 | 10 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8474): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0007 | 0/0 | 8479 | 11 | 0 | 0 | 11 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8474): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0011 | 0/0 | 8482 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8477): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0012 | 0/0 | 8478 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8473): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0018 | 0/0 | 8480 | 3 | 0 | 0 | 2 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8475): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0021 | 0/0 | 8480 | 2 | 0 | 0 | 1 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8475): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0031 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0038 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0040 | 0/0 | 8475 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8470): Show |
chr11 | 74325316 | 74403433 |
| a0003c0003t0042 | 0/0 | 8479 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8474): Show |
chr11 | 74325316 | 74403433 |
| a0003c0006t0013 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0003c0006t0015 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0003c0006t0048 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0004c0005t0014 | 0/0 | 8476 | 5 | 0 | 1 | 0 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0004c0005t0047 | 0/0 | 8476 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0004c0005t0050 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0005c0007t0005 | 0/0 | 8477 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0005c0007t0055 | 0/0 | 8477 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0006c0012t0005 | 0/0 | 8477 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0007c0010t0025 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0008c0014t0016 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8471): Show |
chr11 | 74325316 | 74403433 |
| a0009c0011t0026 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8472): Show |
chr11 | 74325316 | 74403433 |
| a0010c0008t0001 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | ATCTG others(8476): Show |
chr11 | 74325316 | 74403433 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0020g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0020g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0022g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0022g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0030g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0033g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0034g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0035g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0036g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0037g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0039g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0041g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0043g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0044g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0045g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0016g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0016g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0016g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0019g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0019g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0019g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0023g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0023g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0024g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0024g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0025g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0026g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0029g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0046g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0049g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0058g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0059g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0060g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0009t0029g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0013t0032g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0027g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0027g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0028g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0028g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0051g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0052g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0053g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0054g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0056g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0057g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0011g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0018g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0018g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0021g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0021g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0031g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0038g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0040g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0042g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0006t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0006t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0006t0048g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0047g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0050g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0005c0007t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0005c0007t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0005c0007t0055g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0006c0012t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0007c0010t0025g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0008c0014t0016g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0009c0011t0026g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0010c0008t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0011 | g0308 | EUR | GBR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00140 | hp2 | a0002 | c0002 | t0004 | g0295 | EUR | GBR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00280 | hp1 | a0003 | c0003 | t0002 | g0001 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0312 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0256 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0035 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00423 | hp1 | a0003 | c0003 | t0012 | g0037 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00438 | hp2 | a0003 | c0003 | t0006 | g0043 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0031 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00597 | hp1 | a0003 | c0003 | t0012 | g0063 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00597 | hp2 | a0002 | c0002 | t0005 | g0275 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00609 | hp2 | a0003 | c0003 | t0012 | g0049 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00621 | hp1 | a0003 | c0003 | t0002 | g0075 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0326 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00639 | hp2 | a0001 | c0004 | t0023 | g0178 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00642 | hp2 | a0004 | c0005 | t0047 | g0185 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00673 | hp2 | a0003 | c0003 | t0002 | g0039 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00733 | hp2 | a0002 | c0002 | t0005 | g0288 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00735 | hp1 | a0002 | c0002 | t0005 | g0313 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0310 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00738 | hp1 | a0003 | c0003 | t0042 | g0069 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00738 | hp2 | a0002 | c0002 | t0005 | g0280 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0285 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01069 | hp1 | a0002 | c0002 | t0005 | g0287 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01074 | hp1 | a0001 | c0004 | t0019 | g0103 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01074 | hp2 | a0002 | c0002 | t0004 | g0241 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01081 | hp1 | a0002 | c0002 | t0057 | g0224 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01081 | hp2 | a0001 | c0001 | t0036 | g0227 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01099 | hp1 | a0001 | c0004 | t0029 | g0359 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01099 | hp2 | a0001 | c0004 | t0010 | g0010 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0192 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0305 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01175 | hp1 | a0003 | c0003 | t0006 | g0072 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01243 | hp2 | a0001 | c0004 | t0017 | g0360 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01257 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01261 | hp1 | a0004 | c0005 | t0014 | g0181 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01261 | hp2 | a0002 | c0002 | t0005 | g0332 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01361 | hp1 | a0002 | c0002 | t0054 | g0325 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01433 | hp1 | a0002 | c0002 | t0005 | g0218 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01516 | hp1 | a0002 | c0002 | t0004 | g0302 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0009 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0331 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01517 | hp2 | a0003 | c0003 | t0002 | g0062 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01884 | hp1 | a0001 | c0004 | t0008 | g0340 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01884 | hp2 | a0001 | c0004 | t0015 | g0096 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0198 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02004 | hp1 | a0003 | c0003 | t0011 | g0089 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02015 | hp1 | a0005 | c0007 | t0005 | g0054 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02015 | hp2 | a0003 | c0003 | t0012 | g0047 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02027 | hp2 | a0002 | c0002 | t0004 | g0220 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02040 | hp1 | a0003 | c0003 | t0002 | g0066 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02040 | hp2 | a0002 | c0002 | t0005 | g0258 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0296 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0170 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02056 | hp1 | a0002 | c0002 | t0005 | g0291 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02074 | hp1 | a0003 | c0003 | t0021 | g0034 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02074 | hp2 | a0002 | c0002 | t0005 | g0229 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02080 | hp1 | a0003 | c0003 | t0002 | g0042 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02080 | hp2 | a0001 | c0001 | t0020 | g0114 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02129 | hp1 | a0003 | c0003 | t0002 | g0029 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0041 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0194 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02148 | hp2 | a0002 | c0002 | t0004 | g0246 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02165 | hp1 | a0005 | c0007 | t0005 | g0067 | EAS | CDX | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02257 | hp1 | a0001 | c0004 | t0008 | g0339 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02258 | hp1 | a0001 | c0004 | t0013 | g0336 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02258 | hp2 | a0001 | c0004 | t0008 | g0014 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02280 | hp1 | a0001 | c0004 | t0058 | g0355 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0186 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02293 | hp1 | a0003 | c0003 | t0006 | g0052 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02300 | hp1 | a0002 | c0002 | t0005 | g0283 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02451 | hp1 | a0001 | c0004 | t0017 | g0356 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02451 | hp2 | a0002 | c0002 | t0004 | g0100 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02523 | hp1 | a0003 | c0003 | t0007 | g0023 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02572 | hp1 | a0001 | c0004 | t0025 | g0343 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02572 | hp2 | a0001 | c0013 | t0032 | g0169 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0309 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02602 | hp2 | a0002 | c0002 | t0005 | g0149 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02615 | hp1 | a0001 | c0001 | t0022 | g0354 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02615 | hp2 | a0001 | c0001 | t0041 | g0188 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02622 | hp1 | a0001 | c0001 | t0022 | g0353 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02622 | hp2 | a0001 | c0004 | t0009 | g0160 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02630 | hp1 | a0003 | c0003 | t0002 | g0028 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02630 | hp2 | a0001 | c0004 | t0013 | g0337 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0314 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02647 | hp2 | a0001 | c0004 | t0009 | g0168 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02698 | hp2 | a0002 | c0002 | t0005 | g0158 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02717 | hp1 | a0001 | c0004 | t0008 | g0338 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02717 | hp2 | a0001 | c0004 | t0016 | g0346 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02723 | hp1 | a0001 | c0004 | t0008 | g0015 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02723 | hp2 | a0001 | c0004 | t0016 | g0348 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02735 | hp1 | a0004 | c0005 | t0014 | g0180 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02809 | hp1 | a0001 | c0004 | t0009 | g0166 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02809 | hp2 | a0003 | c0006 | t0048 | g0027 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02818 | hp1 | a0001 | c0004 | t0019 | g0104 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02818 | hp2 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02886 | hp1 | a0003 | c0006 | t0015 | g0026 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02886 | hp2 | a0002 | c0002 | t0004 | g0190 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02895 | hp1 | a0001 | c0009 | t0029 | g0358 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02895 | hp2 | a0001 | c0004 | t0009 | g0162 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0011 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02897 | hp1 | a0001 | c0004 | t0009 | g0161 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0011 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02922 | hp1 | a0002 | c0002 | t0004 | g0248 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02922 | hp2 | a0001 | c0004 | t0009 | g0163 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02965 | hp1 | a0001 | c0001 | t0039 | g0117 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02965 | hp2 | a0001 | c0004 | t0024 | g0334 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0199 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02970 | hp2 | a0001 | c0004 | t0008 | g0342 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02976 | hp1 | a0001 | c0004 | t0008 | g0014 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02976 | hp2 | a0001 | c0004 | t0009 | g0164 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0090 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03041 | hp1 | a0001 | c0001 | t0043 | g0151 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03041 | hp2 | a0001 | c0004 | t0008 | g0015 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03098 | hp1 | a0001 | c0004 | t0060 | g0362 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03098 | hp2 | a0001 | c0004 | t0026 | g0213 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0193 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03130 | hp2 | a0001 | c0004 | t0015 | g0094 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03139 | hp2 | a0003 | c0003 | t0002 | g0078 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03195 | hp1 | a0001 | c0004 | t0008 | g0013 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03195 | hp2 | a0001 | c0004 | t0013 | g0335 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03209 | hp1 | a0001 | c0004 | t0015 | g0095 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03209 | hp2 | a0001 | c0004 | t0010 | g0010 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03225 | hp1 | a0001 | c0004 | t0008 | g0341 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03225 | hp2 | a0003 | c0003 | t0002 | g0007 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03239 | hp1 | a0006 | c0012 | t0005 | g0142 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03239 | hp2 | a0003 | c0003 | t0002 | g0087 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0351 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03453 | hp2 | a0001 | c0004 | t0009 | g0165 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0350 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03486 | hp2 | a0007 | c0010 | t0025 | g0344 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03490 | hp2 | a0001 | c0001 | t0044 | g0101 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03491 | hp1 | a0003 | c0003 | t0002 | g0048 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03491 | hp2 | a0004 | c0005 | t0014 | g0182 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03492 | hp2 | a0004 | c0005 | t0014 | g0184 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0093 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03516 | hp2 | a0008 | c0014 | t0016 | g0347 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03540 | hp2 | a0002 | c0002 | t0004 | g0197 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03579 | hp1 | a0001 | c0004 | t0009 | g0167 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03579 | hp2 | a0001 | c0004 | t0017 | g0357 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03654 | hp1 | a0003 | c0003 | t0006 | g0006 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0221 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03669 | hp2 | a0001 | c0001 | t0033 | g0223 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03710 | hp1 | a0003 | c0003 | t0003 | g0068 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03710 | hp2 | a0002 | c0002 | t0005 | g0123 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03831 | hp1 | a0001 | c0004 | t0049 | g0153 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03834 | hp1 | a0002 | c0002 | t0004 | g0297 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0293 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03927 | hp1 | a0003 | c0003 | t0021 | g0033 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03942 | hp1 | a0001 | c0001 | t0037 | g0327 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03942 | hp2 | a0002 | c0002 | t0004 | g0245 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04184 | hp2 | a0003 | c0003 | t0018 | g0038 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0086 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0328 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04204 | hp1 | a0002 | c0002 | t0005 | g0147 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04204 | hp2 | a0004 | c0005 | t0014 | g0183 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04228 | hp1 | a0001 | c0004 | t0010 | g0174 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18522 | hp1 | a0003 | c0003 | t0040 | g0025 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18522 | hp2 | a0009 | c0011 | t0026 | g0214 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0286 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18747 | hp1 | a0002 | c0002 | t0005 | g0255 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18906 | hp1 | a0001 | c0004 | t0017 | g0361 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18906 | hp2 | a0002 | c0002 | t0004 | g0177 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18941 | hp1 | a0002 | c0002 | t0005 | g0289 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18942 | hp1 | a0002 | c0002 | t0005 | g0217 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18943 | hp2 | a0001 | c0004 | t0010 | g0175 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18944 | hp1 | a0003 | c0003 | t0006 | g0077 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18945 | hp2 | a0002 | c0002 | t0005 | g0250 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18946 | hp1 | a0002 | c0002 | t0005 | g0290 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18947 | hp1 | a0002 | c0002 | t0005 | g0315 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0088 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18948 | hp2 | a0002 | c0002 | t0005 | g0012 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18949 | hp2 | a0003 | c0003 | t0006 | g0076 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18950 | hp1 | a0003 | c0003 | t0002 | g0059 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0244 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18952 | hp1 | a0005 | c0007 | t0055 | g0053 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18952 | hp2 | a0010 | c0008 | t0001 | g0079 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18953 | hp1 | a0002 | c0002 | t0004 | g0233 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18954 | hp1 | a0002 | c0002 | t0027 | g0278 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18956 | hp2 | a0002 | c0002 | t0004 | g0322 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18957 | hp1 | a0003 | c0003 | t0006 | g0071 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18957 | hp2 | a0002 | c0002 | t0005 | g0277 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18959 | hp1 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18959 | hp2 | a0003 | c0003 | t0031 | g0022 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18960 | hp1 | a0002 | c0002 | t0004 | g0299 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18960 | hp2 | a0002 | c0002 | t0005 | g0125 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18962 | hp1 | a0002 | c0002 | t0028 | g0252 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18962 | hp2 | a0003 | c0003 | t0006 | g0006 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18963 | hp1 | a0003 | c0003 | t0002 | g0060 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18963 | hp2 | a0002 | c0002 | t0004 | g0301 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18965 | hp1 | a0002 | c0002 | t0004 | g0321 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18965 | hp2 | a0001 | c0001 | t0045 | g0132 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18966 | hp2 | a0002 | c0002 | t0005 | g0316 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18969 | hp2 | a0003 | c0003 | t0038 | g0050 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18970 | hp1 | a0003 | c0003 | t0002 | g0084 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18970 | hp2 | a0002 | c0002 | t0004 | g0243 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18977 | hp1 | a0001 | c0004 | t0010 | g0176 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18977 | hp2 | a0003 | c0003 | t0007 | g0004 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18978 | hp1 | a0003 | c0003 | t0018 | g0083 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0159 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0073 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18981 | hp1 | a0002 | c0002 | t0005 | g0292 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18982 | hp1 | a0003 | c0003 | t0002 | g0045 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18982 | hp2 | a0002 | c0002 | t0005 | g0281 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18983 | hp1 | a0003 | c0003 | t0007 | g0004 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18984 | hp1 | a0001 | c0004 | t0010 | g0171 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18987 | hp1 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18988 | hp2 | a0003 | c0003 | t0002 | g0051 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0074 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18994 | hp1 | a0002 | c0002 | t0004 | g0303 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18997 | hp1 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18997 | hp2 | a0002 | c0002 | t0005 | g0294 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0056 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18998 | hp2 | a0002 | c0002 | t0004 | g0239 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18999 | hp1 | a0001 | c0004 | t0010 | g0172 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19000 | hp2 | a0002 | c0002 | t0005 | g0298 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19001 | hp1 | a0001 | c0001 | t0020 | g0134 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19001 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19002 | hp1 | a0002 | c0002 | t0005 | g0253 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19003 | hp1 | a0002 | c0002 | t0028 | g0225 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19003 | hp2 | a0001 | c0004 | t0010 | g0173 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19004 | hp2 | a0003 | c0003 | t0006 | g0030 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19005 | hp1 | a0003 | c0003 | t0007 | g0021 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19007 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19009 | hp1 | a0002 | c0002 | t0005 | g0249 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0058 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19011 | hp1 | a0003 | c0003 | t0007 | g0020 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0196 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0195 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19058 | hp1 | a0002 | c0002 | t0005 | g0284 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19060 | hp1 | a0003 | c0003 | t0018 | g0040 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19060 | hp2 | a0002 | c0002 | t0056 | g0274 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19062 | hp1 | a0003 | c0003 | t0007 | g0018 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19062 | hp2 | a0002 | c0002 | t0004 | g0240 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19063 | hp1 | a0002 | c0002 | t0004 | g0323 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19063 | hp2 | a0001 | c0001 | t0035 | g0320 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19064 | hp1 | a0002 | c0002 | t0005 | g0251 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19066 | hp2 | a0003 | c0003 | t0007 | g0024 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19070 | hp1 | a0003 | c0003 | t0006 | g0061 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19070 | hp2 | a0002 | c0002 | t0004 | g0300 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19074 | hp1 | a0003 | c0003 | t0007 | g0003 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19074 | hp2 | a0002 | c0002 | t0004 | g0238 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19075 | hp1 | a0002 | c0002 | t0004 | g0317 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19075 | hp2 | a0003 | c0003 | t0002 | g0032 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19076 | hp2 | a0003 | c0003 | t0007 | g0019 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19077 | hp1 | a0002 | c0002 | t0004 | g0236 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19077 | hp2 | a0003 | c0003 | t0002 | g0055 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19078 | hp1 | a0002 | c0002 | t0005 | g0282 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19079 | hp2 | a0003 | c0003 | t0006 | g0064 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19080 | hp1 | a0003 | c0003 | t0007 | g0017 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19080 | hp2 | a0002 | c0002 | t0005 | g0254 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19081 | hp1 | a0002 | c0002 | t0005 | g0012 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19081 | hp2 | a0003 | c0003 | t0006 | g0044 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19083 | hp1 | a0003 | c0003 | t0007 | g0003 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19085 | hp2 | a0002 | c0002 | t0052 | g0237 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19086 | hp1 | a0002 | c0002 | t0027 | g0279 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19088 | hp1 | a0003 | c0003 | t0006 | g0036 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19089 | hp1 | a0003 | c0003 | t0012 | g0065 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19240 | hp1 | a0001 | c0004 | t0019 | g0105 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19240 | hp2 | a0001 | c0004 | t0008 | g0013 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0266 | EUR | TSI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20752 | hp2 | a0002 | c0002 | t0051 | g0324 | EUR | TSI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | GIH | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20905 | hp2 | a0002 | c0002 | t0004 | g0124 | SAS | GIH | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0082 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0306 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02109 | hp1 | a0001 | c0004 | t0059 | g0363 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0267 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02486 | hp1 | a0004 | c0005 | t0050 | g0179 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02486 | hp2 | a0001 | c0004 | t0013 | g0333 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02559 | hp1 | a0001 | c0004 | t0024 | g0345 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03471 | hp1 | a0003 | c0006 | t0013 | g0091 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0191 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18955 | hp1 | a0002 | c0002 | t0053 | g0228 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20300 | hp1 | a0001 | c0004 | t0023 | g0259 | AFR | USA | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20300 | hp2 | a0001 | c0004 | t0016 | g0349 | AFR | USA | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA21309 | hp1 | a0001 | c0001 | t0034 | g0208 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA21309 | hp2 | a0001 | c0004 | t0046 | g0352 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0030 | g0016 | REF | REF | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0005 | g0150 | REF | REF | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74336698 | T | A | 1 | a0004 | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
missense_variant | MODERATE | c.1823A>T | p.Asn608Ile | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2095/8477 | 1823/1869 | 608/622 | chr11 | 74336698 | |||
| chr11:74338592 | C | T | 1 | a0010 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.1642G>A | p.Val548Met | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/14 | 1914/8477 | 1642/1869 | 548/622 | chr11 | 74338592 | |||
| chr11:74342462 | G | A | 1 | a0007 | 1 | HG03486.hp2 | missense_variant&splice_region_variant | MODERATE | c.1631C>T | p.Ser544Leu | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/14 | 1903/8477 | 1631/1869 | 544/622 | chr11 | 74342462 | |||
| chr11:74342502 | C | T | 7 | a0001 a0003 a0004 others(4): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
missense_variant | MODERATE | c.1591G>A | p.Val531Ile | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/14 | 1863/8477 | 1591/1869 | 531/622 | chr11 | 74342502 | |||
| chr11:74342578 | T | G | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1515A>C | p.Glu505Asp | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/14 | 1787/8477 | 1515/1869 | 505/622 | chr11 | 74342578 | |||
| chr11:74342922 | T | C | 1 | a0006 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1405A>G | p.Ile469Val | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 11/14 | 1677/8477 | 1405/1869 | 469/622 | chr11 | 74342922 | |||
| chr11:74351455 | G | A | 1 | a0008 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.677C>T | p.Pro226Leu | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/14 | 949/8477 | 677/1869 | 226/622 | chr11 | 74351455 | |||
| chr11:74398121 | A | G | 3 | a0003 a0005 a0010 |
93 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
missense_variant | MODERATE | c.41T>C | p.Leu14Pro | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/14 | 313/8477 | 41/1869 | 14/622 | chr11 | 74398121 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74338524 | A | G | 3 | a0001c0001 a0003c0003 a0010c0008 |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
synonymous_variant | LOW | c.1710T>C | p.Ser570Ser | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/14 | 1982/8477 | 1710/1869 | 570/622 | chr11 | 74338524 | |||
| chr11:74343336 | A | G | 1 | a0001c0009 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1299T>C | p.Phe433Phe | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 10/14 | 1571/8477 | 1299/1869 | 433/622 | chr11 | 74343336 | |||
| chr11:74346752 | T | C | 1 | a0001c0013 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1017A>G | p.Ala339Ala | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/14 | 1289/8477 | 1017/1869 | 339/622 | chr11 | 74346752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74330438 | T | C | 2 | a0001c0001t0041 a0003c0003t0040 |
2 | HG02615.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6214A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6214 | chr11 | 74330438 | ||||||
| chr11:74330539 | A | C | 2 | a0001c0004t0016 a0008c0014t0016 |
4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6113T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6113 | chr11 | 74330539 | ||||||
| chr11:74330547 | A | T | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(60): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*6105T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6105 | chr11 | 74330547 | ||||||
| chr11:74330567 | A | C | 1 | a0003c0003t0006 | 13 | HG00438.hp2 HG01175.hp1 HG02293.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6085T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6085 | chr11 | 74330567 | ||||||
| chr11:74330873 | C | G | 1 | a0002c0002t0052 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5779G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5779 | chr11 | 74330873 | ||||||
| chr11:74331013 | T | A | 1 | a0001c0001t0035 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5639A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5639 | chr11 | 74331013 | ||||||
| chr11:74331123 | G | A | 3 | a0004c0005t0014 a0004c0005t0047 a0004c0005t0050 |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5529C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5529 | chr11 | 74331123 | ||||||
| chr11:74331196 | A | G | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*5456T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5456 | chr11 | 74331196 | ||||||
| chr11:74331241 | G | A | 11 | a0001c0004t0009 a0001c0004t0013 a0001c0004t0016 others(8): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5411C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5411 | chr11 | 74331241 | ||||||
| chr11:74331263 | C | CTTTT | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(18): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*5385_*5388dupAAAA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5388 | chr11 | 74331263 | ||||||
| chr11:74331263 | C | CTTTTT | 5 | a0001c0001t0011 a0001c0001t0020 a0001c0004t0049 others(2): Show |
11 | HG00140.hp1 HG01106.hp2 HG01517.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5384_*5388dupAAAA others(1): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5388 | chr11 | 74331263 | ||||||
| chr11:74331263 | CT | C | 14 | a0001c0004t0009 a0001c0004t0013 a0001c0004t0016 others(11): Show |
33 | HG00639.hp2 HG00642.hp2 HG01261.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5388delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5388 | chr11 | 74331263 | ||||||
| chr11:74331284 | T | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*5368A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5368 | chr11 | 74331284 | ||||||
| chr11:74331285 | G | A | 8 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0033 others(5): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5367C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5367 | chr11 | 74331285 | ||||||
| chr11:74331336 | C | A | 11 | a0001c0004t0009 a0001c0004t0013 a0001c0004t0016 others(8): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5316G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5316 | chr11 | 74331336 | ||||||
| chr11:74331453 | G | C | 1 | a0002c0002t0054 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5199C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5199 | chr11 | 74331453 | ||||||
| chr11:74331489 | C | T | 1 | a0001c0004t0019 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5163G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5163 | chr11 | 74331489 | ||||||
| chr11:74331513 | C | T | 2 | a0001c0004t0019 a0001c0013t0032 |
4 | HG01074.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5139G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5139 | chr11 | 74331513 | ||||||
| chr11:74331622 | G | C | 10 | a0001c0001t0002 a0001c0001t0044 a0003c0003t0002 others(7): Show |
86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*5030C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5030 | chr11 | 74331622 | ||||||
| chr11:74331672 | G | C | 1 | a0001c0001t0037 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4980C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4980 | chr11 | 74331672 | ||||||
| chr11:74331742 | A | G | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(41): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*4910T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4910 | chr11 | 74331742 | ||||||
| chr11:74332085 | G | A | 1 | a0005c0007t0055 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4567C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4567 | chr11 | 74332085 | ||||||
| chr11:74332126 | A | G | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*4526T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4526 | chr11 | 74332126 | ||||||
| chr11:74332205 | A | G | 11 | a0001c0004t0009 a0001c0004t0013 a0001c0004t0016 others(8): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4447T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4447 | chr11 | 74332205 | ||||||
| chr11:74332216 | A | T | 1 | a0002c0002t0027 | 2 | NA18954.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4436T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4436 | chr11 | 74332216 | ||||||
| chr11:74332663 | G | A | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*3989C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3989 | chr11 | 74332663 | ||||||
| chr11:74332669 | A | G | 1 | a0003c0003t0042 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3983T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3983 | chr11 | 74332669 | ||||||
| chr11:74332727 | T | C | 1 | a0001c0001t0041 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3925A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3925 | chr11 | 74332727 | ||||||
| chr11:74332937 | G | T | 2 | a0004c0005t0014 a0004c0005t0047 |
6 | HG00642.hp2 HG01261.hp1 HG02735.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3715C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3715 | chr11 | 74332937 | ||||||
| chr11:74332949 | TAA | T | 1 | a0001c0004t0009 | 9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3701_*3702delTT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3701 | chr11 | 74332949 | ||||||
| chr11:74333094 | G | A | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*3558C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3558 | chr11 | 74333094 | ||||||
| chr11:74333111 | T | TA | 11 | a0001c0004t0009 a0001c0004t0013 a0001c0004t0016 others(8): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3540dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3540 | chr11 | 74333111 | ||||||
| chr11:74333188 | TA | T | 1 | a0001c0004t0019 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3463delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3463 | chr11 | 74333188 | ||||||
| chr11:74333420 | C | T | 1 | a0001c0004t0019 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3232G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3232 | chr11 | 74333420 | ||||||
| chr11:74333512 | C | T | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*3140G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3140 | chr11 | 74333512 | ||||||
| chr11:74333646 | T | C | 2 | a0001c0004t0029 a0001c0009t0029 |
2 | HG01099.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3006A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3006 | chr11 | 74333646 | ||||||
| chr11:74333815 | A | C | 1 | a0002c0002t0051 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2837T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2837 | chr11 | 74333815 | ||||||
| chr11:74333930 | C | G | 11 | a0001c0004t0009 a0001c0004t0013 a0001c0004t0016 others(8): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2722G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2722 | chr11 | 74333930 | ||||||
| chr11:74333931 | C | T | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(13): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2721G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2721 | chr11 | 74333931 | ||||||
| chr11:74333982 | C | G | 2 | a0001c0004t0025 a0007c0010t0025 |
2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2670G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2670 | chr11 | 74333982 | ||||||
| chr11:74334238 | T | A | 5 | a0001c0004t0013 a0001c0004t0024 a0001c0004t0060 others(2): Show |
9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2414A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2414 | chr11 | 74334238 | ||||||
| chr11:74334359 | C | G | 1 | a0001c0004t0008 | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2293G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2293 | chr11 | 74334359 | ||||||
| chr11:74334697 | A | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(15): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1955 | chr11 | 74334697 | ||||||
| chr11:74334807 | G | C | 1 | a0004c0005t0050 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1845C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1845 | chr11 | 74334807 | ||||||
| chr11:74334907 | CT | C | 20 | a0001c0001t0039 a0001c0004t0008 a0001c0004t0009 others(17): Show |
52 | HG00639.hp2 HG00642.hp2 HG01074.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1744delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1744 | chr11 | 74334907 | ||||||
| chr11:74334907 | CTT | C | 11 | a0001c0001t0002 a0001c0001t0041 a0001c0001t0043 others(8): Show |
83 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1743_*1744delAA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1743 | chr11 | 74334907 | ||||||
| chr11:74334907 | CTTT | C | 2 | a0001c0001t0022 a0003c0003t0012 |
7 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1742_*1744delAAA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1742 | chr11 | 74334907 | ||||||
| chr11:74335005 | G | A | 3 | a0004c0005t0014 a0004c0005t0047 a0004c0005t0050 |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1647C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1647 | chr11 | 74335005 | ||||||
| chr11:74335061 | G | A | 1 | a0002c0002t0056 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1591C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1591 | chr11 | 74335061 | ||||||
| chr11:74335234 | G | A | 1 | a0002c0002t0057 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1418 | chr11 | 74335234 | ||||||
| chr11:74335237 | T | C | 1 | a0003c0006t0048 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1415A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1415 | chr11 | 74335237 | ||||||
| chr11:74335288 | A | G | 2 | a0001c0004t0026 a0009c0011t0026 |
2 | HG03098.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1364T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1364 | chr11 | 74335288 | ||||||
| chr11:74335319 | A | T | 1 | a0001c0001t0034 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1333 | chr11 | 74335319 | ||||||
| chr11:74335321 | C | A | 1 | a0001c0001t0034 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1331 | chr11 | 74335321 | ||||||
| chr11:74335323 | T | A | 1 | a0001c0001t0034 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1329 | chr11 | 74335323 | ||||||
| chr11:74335324 | A | C | 1 | a0001c0001t0034 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1328T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1328 | chr11 | 74335324 | ||||||
| chr11:74335546 | T | C | 1 | a0001c0001t0045 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1106A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1106 | chr11 | 74335546 | ||||||
| chr11:74335638 | C | CA | 3 | a0004c0005t0014 a0004c0005t0047 a0004c0005t0050 |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1013dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1013 | chr11 | 74335638 | ||||||
| chr11:74335713 | A | T | 2 | a0001c0004t0025 a0007c0010t0025 |
2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*939T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 939 | chr11 | 74335713 | ||||||
| chr11:74335816 | C | T | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*836G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 836 | chr11 | 74335816 | ||||||
| chr11:74335930 | C | T | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
262 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*722G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 722 | chr11 | 74335930 | ||||||
| chr11:74336181 | C | G | 11 | a0001c0004t0009 a0001c0004t0013 a0001c0004t0016 others(8): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*471G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 471 | chr11 | 74336181 | ||||||
| chr11:74336198 | A | C | 1 | a0004c0005t0047 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 454 | chr11 | 74336198 | ||||||
| chr11:74336219 | C | G | 2 | a0001c0004t0010 a0001c0004t0058 |
9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 433 | chr11 | 74336219 | ||||||
| chr11:74336249 | C | T | 1 | a0001c0013t0032 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*403G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 403 | chr11 | 74336249 | ||||||
| chr11:74336311 | C | T | 1 | a0001c0001t0033 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 341 | chr11 | 74336311 | ||||||
| chr11:74336417 | TA | T | 2 | a0001c0004t0015 a0003c0006t0015 |
4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*234delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 234 | chr11 | 74336417 | ||||||
| chr11:74336453 | C | T | 1 | a0001c0004t0046 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 199 | chr11 | 74336453 | ||||||
| chr11:74336552 | A | C | 1 | a0001c0013t0032 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 100 | chr11 | 74336552 | ||||||
| chr11:74336638 | A | G | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(30): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 14 | chr11 | 74336638 | ||||||
| chr11:74398186 | G | T | 2 | a0003c0003t0007 a0003c0003t0031 |
12 | HG02523.hp1 NA18959.hp2 NA18977.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-25C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/14 | 25 | chr11 | 74398186 | ||||||
| chr11:74398213 | G | A | 6 | a0001c0004t0017 a0001c0004t0029 a0001c0004t0058 others(3): Show |
9 | HG01099.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-52C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/14 | 52 | chr11 | 74398213 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74336824 | A | AT | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1767-71dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74336824 | |||||||
| chr11:74336953 | G | A | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1767-199C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74336953 | |||||||
| chr11:74336966 | A | G | 2 | a0001c0004t0025g0343 a0007c0010t0025g0344 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1767-212T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74336966 | |||||||
| chr11:74337177 | G | A | 1 | a0001c0001t0003g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1767-423C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337177 | |||||||
| chr11:74337243 | C | T | 8 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(5): Show |
9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1767-489G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337243 | |||||||
| chr11:74337262 | A | G | 1 | a0003c0003t0002g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1767-508T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337262 | |||||||
| chr11:74337356 | C | A | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1767-602G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337356 | |||||||
| chr11:74337428 | C | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1767-674G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337428 | |||||||
| chr11:74337449 | C | T | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1767-695G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337449 | |||||||
| chr11:74337765 | C | A | 2 | a0003c0003t0007g0018 a0003c0003t0007g0023 |
2 | HG02523.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1766+703G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337765 | |||||||
| chr11:74337858 | T | A | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1766+610A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337858 | |||||||
| chr11:74338763 | G | A | 14 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(11): Show |
15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1633-162C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338763 | |||||||
| chr11:74338863 | C | G | 1 | a0001c0001t0003g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1633-262G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338863 | |||||||
| chr11:74338997 | A | G | 1 | a0001c0001t0003g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1633-396T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338997 | |||||||
| chr11:74338997 | A | T | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633-396T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338997 | |||||||
| chr11:74339128 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(231): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1633-527T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339128 | |||||||
| chr11:74339164 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1633-563C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339164 | |||||||
| chr11:74339204 | G | A | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1633-603C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339204 | |||||||
| chr11:74339217 | C | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(260): Show |
278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.1633-616G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339217 | |||||||
| chr11:74339321 | C | T | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633-720G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339321 | |||||||
| chr11:74339694 | C | G | 6 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0200 others(3): Show |
6 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.1633-1093G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339694 | |||||||
| chr11:74339810 | G | A | 2 | a0001c0001t0011g0331 a0003c0003t0011g0089 |
2 | HG01517.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1633-1209C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339810 | |||||||
| chr11:74340015 | C | T | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633-1414G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340015 | |||||||
| chr11:74340071 | A | G | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633-1470T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340071 | |||||||
| chr11:74340340 | A | G | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633-1739T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340340 | |||||||
| chr11:74340487 | G | A | 1 | a0002c0002t0005g0286 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1633-1886C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340487 | |||||||
| chr11:74340569 | C | A | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1632+1892G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340569 | |||||||
| chr11:74340639 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1632+1822A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340639 | |||||||
| chr11:74340999 | G | C | 1 | a0001c0001t0003g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1632+1462C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340999 | |||||||
| chr11:74341154 | T | C | 3 | a0002c0002t0004g0093 a0002c0002t0004g0170 a0002c0002t0004g0177 |
3 | HG02055.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1632+1307A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341154 | |||||||
| chr11:74341219 | C | G | 15 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(12): Show |
16 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1632+1242G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341219 | |||||||
| chr11:74341312 | T | G | 1 | a0001c0004t0059g0363 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1632+1149A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341312 | |||||||
| chr11:74341351 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0207 a0001c0001t0020g0134 |
3 | HG02004.hp2 HG02148.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1632+1110T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341351 | |||||||
| chr11:74341418 | G | A | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1632+1043C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341418 | |||||||
| chr11:74341537 | C | T | 2 | a0002c0002t0005g0287 a0002c0002t0005g0313 |
2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1632+924G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341537 | |||||||
| chr11:74341567 | C | G | 5 | a0001c0004t0008g0014 a0001c0004t0008g0338 a0001c0004t0008g0339 others(2): Show |
6 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1632+894G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341567 | |||||||
| chr11:74341651 | C | G | 1 | a0001c0001t0003g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1632+810G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341651 | |||||||
| chr11:74341695 | G | GA | 119 | a0001c0001t0002g0099 a0001c0001t0002g0126 a0001c0001t0002g0152 others(116): Show |
129 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1632+765dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341695 | |||||||
| chr11:74341695 | G | GAA | 11 | a0001c0001t0002g0107 a0001c0004t0009g0160 a0001c0004t0009g0167 others(8): Show |
12 | HG02055.hp2 HG02074.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1632+764_1632+765d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341695 | |||||||
| chr11:74341695 | GA | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(112): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1632+765delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341695 | |||||||
| chr11:74341825 | T | A | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1632+636A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341825 | |||||||
| chr11:74342151 | T | C | 2 | a0003c0003t0002g0045 a0003c0003t0002g0060 |
2 | NA18963.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1632+310A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74342151 | |||||||
| chr11:74342833 | A | C | 9 | a0002c0002t0005g0012 a0002c0002t0005g0159 a0002c0002t0005g0217 others(6): Show |
10 | NA18942.hp1 NA18946.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.1442+52T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 11/13 | chr11 | 74342833 | |||||||
| chr11:74343130 | A | G | 13 | a0002c0002t0004g0233 a0002c0002t0004g0295 a0002c0002t0004g0297 others(10): Show |
13 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1313-116T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 10/13 | chr11 | 74343130 | |||||||
| chr11:74343301 | G | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(221): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1312+22C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 10/13 | chr11 | 74343301 | |||||||
| chr11:74343453 | G | C | 2 | a0001c0001t0003g0264 a0001c0001t0003g0306 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1219-37C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343453 | |||||||
| chr11:74343503 | T | C | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-87A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343503 | |||||||
| chr11:74343572 | A | G | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1219-156T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343572 | |||||||
| chr11:74343769 | C | CT | 51 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(48): Show |
55 | HG00639.hp2 HG01884.hp1 HG02027.hp2 others(52): Show |
intron_variant | MODIFIER | c.1219-354dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | |||||||
| chr11:74343769 | C | CTT | 10 | a0001c0004t0009g0165 a0001c0004t0016g0346 a0001c0004t0060g0362 others(7): Show |
10 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-355_1219-354d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | |||||||
| chr11:74343769 | CT | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(183): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1219-354delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | |||||||
| chr11:74343769 | CTTTTTTT others(3): Show |
C | 1 | a0003c0003t0002g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1219-363_1219-354d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | |||||||
| chr11:74343769 | CTTTTTTT others(5): Show |
C | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1219-365_1219-354d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | |||||||
| chr11:74343802 | G | A | 1 | a0003c0003t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1219-386C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343802 | |||||||
| chr11:74343831 | T | A | 1 | a0003c0003t0002g0092 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1219-415A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343831 | |||||||
| chr11:74343934 | G | A | 231 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(228): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1219-518C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343934 | |||||||
| chr11:74344034 | C | T | 1 | a0001c0001t0022g0353 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1219-618G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344034 | |||||||
| chr11:74344054 | C | T | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1219-638G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344054 | |||||||
| chr11:74344066 | C | T | 9 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1219-650G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344066 | |||||||
| chr11:74344242 | A | T | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-826T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344242 | |||||||
| chr11:74344253 | T | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(112): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1219-837A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344253 | |||||||
| chr11:74344506 | G | A | 1 | a0003c0003t0006g0064 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1218+963C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344506 | |||||||
| chr11:74344539 | C | A | 1 | a0001c0001t0003g0311 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1218+930G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344539 | |||||||
| chr11:74344587 | A | G | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+882T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344587 | |||||||
| chr11:74344760 | T | C | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+709A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344760 | |||||||
| chr11:74344846 | A | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(221): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1218+623T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344846 | |||||||
| chr11:74345075 | A | T | 1 | a0002c0002t0005g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1218+394T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345075 | |||||||
| chr11:74345284 | C | T | 1 | a0001c0009t0029g0358 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1218+185G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345284 | |||||||
| chr11:74345308 | AG | A | 4 | a0001c0001t0011g0305 a0001c0001t0011g0308 a0001c0001t0011g0331 others(1): Show |
4 | HG00140.hp1 HG01106.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+160delC | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345308 | |||||||
| chr11:74345341 | T | C | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1218+128A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345341 | |||||||
| chr11:74345424 | G | T | 1 | a0001c0004t0060g0362 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1218+45C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345424 | |||||||
| chr11:74345677 | A | G | 1 | a0009c0011t0026g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1038-28T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345677 | |||||||
| chr11:74345804 | T | A | 1 | a0004c0005t0014g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1038-155A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345804 | |||||||
| chr11:74345812 | G | A | 3 | a0002c0002t0004g0093 a0002c0002t0004g0170 a0002c0002t0004g0177 |
3 | HG02055.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1038-163C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345812 | |||||||
| chr11:74345839 | C | T | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1038-190G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345839 | |||||||
| chr11:74345986 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG00323.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1038-337C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345986 | |||||||
| chr11:74346023 | G | T | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038-374C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346023 | |||||||
| chr11:74346191 | G | C | 3 | a0003c0003t0002g0007 a0003c0003t0002g0028 a0003c0003t0002g0078 |
4 | HG02630.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037+541C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346191 | |||||||
| chr11:74346270 | C | CA | 27 | a0002c0002t0004g0011 a0002c0002t0004g0093 a0002c0002t0004g0190 others(24): Show |
28 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1037+461dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | |||||||
| chr11:74346270 | CA | C | 6 | a0001c0004t0025g0343 a0002c0002t0004g0233 a0002c0002t0005g0250 others(3): Show |
6 | HG02572.hp1 HG03486.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037+461delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | |||||||
| chr11:74346270 | CAA | C | 15 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0115 others(12): Show |
15 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1037+460_1037+461d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | |||||||
| chr11:74346270 | CAAA | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(58): Show |
63 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1037+459_1037+461d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | |||||||
| chr11:74346270 | CAAAA | C | 137 | a0001c0001t0001g0119 a0001c0001t0002g0099 a0001c0001t0002g0126 others(134): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1037+458_1037+461d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | |||||||
| chr11:74346270 | CAAAAA | C | 26 | a0001c0001t0041g0188 a0001c0004t0009g0160 a0001c0004t0009g0161 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.1037+457_1037+461d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | |||||||
| chr11:74346270 | CAAAAAAA others(2): Show |
C | 14 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(11): Show |
15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1037+453_1037+461d others(11): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | |||||||
| chr11:74346310 | A | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(112): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1037+422T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346310 | |||||||
| chr11:74346406 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1037+326C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346406 | |||||||
| chr11:74346553 | T | C | 1 | a0001c0001t0003g0311 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1037+179A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346553 | |||||||
| chr11:74346602 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(221): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1037+130A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346602 | |||||||
| chr11:74346693 | A | G | 2 | a0002c0002t0004g0300 a0002c0002t0004g0301 |
2 | NA18963.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1037+39T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346693 | |||||||
| chr11:74346886 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.940-57G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 7/13 | chr11 | 74346886 | |||||||
| chr11:74347613 | T | C | 2 | a0001c0001t0003g0265 a0001c0001t0003g0328 |
2 | HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.750-276A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347613 | |||||||
| chr11:74347665 | T | G | 78 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(75): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.750-328A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347665 | |||||||
| chr11:74347793 | C | G | 1 | a0003c0003t0002g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.750-456G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347793 | |||||||
| chr11:74347822 | C | A | 1 | a0001c0001t0003g0247 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.750-485G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347822 | |||||||
| chr11:74347887 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(263): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.750-550G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347887 | |||||||
| chr11:74347924 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.750-587T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347924 | |||||||
| chr11:74347945 | C | A | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.750-608G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347945 | |||||||
| chr11:74348005 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(221): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.750-668A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348005 | |||||||
| chr11:74348053 | C | T | 1 | a0002c0002t0004g0244 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.750-716G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348053 | |||||||
| chr11:74348126 | T | C | 1 | a0001c0004t0017g0361 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.750-789A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348126 | |||||||
| chr11:74348206 | C | G | 1 | a0002c0002t0005g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.750-869G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348206 | |||||||
| chr11:74348209 | C | T | 1 | a0001c0001t0003g0262 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.750-872G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348209 | |||||||
| chr11:74348303 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.750-966G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348303 | |||||||
| chr11:74348744 | C | T | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.750-1407G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348744 | |||||||
| chr11:74348953 | T | C | 18 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(15): Show |
19 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.750-1616A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348953 | |||||||
| chr11:74348985 | T | G | 10 | a0001c0001t0001g0108 a0001c0001t0001g0130 a0001c0001t0001g0135 others(7): Show |
10 | HG01952.hp2 HG02056.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.750-1648A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348985 | |||||||
| chr11:74349153 | C | T | 7 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 others(4): Show |
7 | HG02004.hp2 HG02148.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.750-1816G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349153 | |||||||
| chr11:74349300 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.750-1963G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349300 | |||||||
| chr11:74349359 | G | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.750-2022C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349359 | |||||||
| chr11:74349557 | G | C | 1 | a0003c0003t0012g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.749+1826C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349557 | |||||||
| chr11:74349784 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.749+1599G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349784 | |||||||
| chr11:74349960 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.749+1423G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349960 | |||||||
| chr11:74350170 | C | G | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.749+1213G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350170 | |||||||
| chr11:74350171 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.749+1212A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350171 | |||||||
| chr11:74350187 | C | T | 4 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 others(1): Show |
4 | HG01074.hp1 HG02280.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.749+1196G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350187 | |||||||
| chr11:74350208 | G | T | 1 | a0001c0009t0029g0358 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.749+1175C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350208 | |||||||
| chr11:74350421 | T | C | 1 | a0002c0002t0005g0275 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.749+962A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350421 | |||||||
| chr11:74350608 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(221): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.749+775C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350608 | |||||||
| chr11:74350617 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(115): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.749+766G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350617 | |||||||
| chr11:74350889 | AAGAAAGA others(3): Show |
A | 2 | a0002c0002t0004g0221 a0002c0002t0004g0246 |
2 | HG02148.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.749+484_749+493del others(10): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350889 | |||||||
| chr11:74350897 | AAG | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(197): Show |
211 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.749+484_749+485del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350897 | |||||||
| chr11:74350897 | AAGAG | A | 4 | a0001c0001t0001g0206 a0001c0001t0003g0231 a0001c0001t0003g0304 others(1): Show |
4 | HG00735.hp2 HG01175.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.749+482_749+485del others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350897 | |||||||
| chr11:74350903 | GAGAGAGA others(9): Show |
G | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.749+464_749+479del others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350903 | |||||||
| chr11:74350905 | GAGAGAGA others(7): Show |
G | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.749+464_749+477del others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350905 | |||||||
| chr11:74350935 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(233): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.749+448C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350935 | |||||||
| chr11:74351064 | A | T | 15 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(12): Show |
16 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.749+319T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351064 | |||||||
| chr11:74351146 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.749+237C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351146 | |||||||
| chr11:74351303 | ACACTTTT others(3): Show |
A | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.749+70_749+79delAT others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351303 | |||||||
| chr11:74351307 | T | C | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.749+76A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351307 | |||||||
| chr11:74351335 | T | C | 1 | a0001c0004t0013g0337 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.749+48A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351335 | |||||||
| chr11:74351340 | C | T | 8 | a0001c0001t0022g0353 a0001c0001t0022g0354 a0001c0004t0017g0356 others(5): Show |
8 | HG01099.hp1 HG01243.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.749+43G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351340 | |||||||
| chr11:74351643 | T | A | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.556-67A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351643 | |||||||
| chr11:74351734 | G | GGGCAGAT others(9): Show |
4 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(1): Show |
4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-174_556-159dup others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351734 | |||||||
| chr11:74351776 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-200G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351776 | |||||||
| chr11:74351840 | T | C | 13 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(10): Show |
13 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.556-264A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351840 | |||||||
| chr11:74351885 | C | G | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.556-309G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351885 | |||||||
| chr11:74351888 | G | A | 4 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(1): Show |
4 | HG01884.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-312C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351888 | |||||||
| chr11:74351961 | C | CA | 16 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(13): Show |
16 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.556-386dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351961 | |||||||
| chr11:74351969 | A | AT | 12 | a0001c0004t0013g0333 a0001c0004t0013g0335 a0001c0004t0013g0336 others(9): Show |
12 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.556-394_556-393ins others(1): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351969 | |||||||
| chr11:74351971 | A | T | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-395T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351971 | |||||||
| chr11:74351972 | AT | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(188): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.556-397delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351972 | |||||||
| chr11:74351973 | T | A | 6 | a0001c0001t0001g0155 a0001c0001t0001g0273 a0001c0004t0025g0343 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-397A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351973 | |||||||
| chr11:74351977 | T | A | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.556-401A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351977 | |||||||
| chr11:74351977 | TAA | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(193): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.556-403_556-402del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351977 | |||||||
| chr11:74352119 | T | C | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-543A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352119 | |||||||
| chr11:74352338 | A | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(233): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.556-762T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352338 | |||||||
| chr11:74352440 | G | T | 80 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(77): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.556-864C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352440 | |||||||
| chr11:74352599 | G | A | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.556-1023C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352599 | |||||||
| chr11:74352764 | C | T | 4 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(1): Show |
4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-1188G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352764 | |||||||
| chr11:74353029 | T | C | 4 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-1453A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353029 | |||||||
| chr11:74353037 | T | TAA | 14 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(11): Show |
15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-1463_556-1462d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353037 | |||||||
| chr11:74353176 | G | GT | 122 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(119): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.556-1601dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353176 | |||||||
| chr11:74353184 | G | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(181): Show |
198 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.556-1608C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353184 | |||||||
| chr11:74353186 | G | T | 27 | a0001c0001t0022g0353 a0001c0001t0022g0354 a0001c0004t0009g0160 others(24): Show |
27 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.556-1610C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353186 | |||||||
| chr11:74353263 | CTTAAT | C | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-1692_556-1688d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353263 | |||||||
| chr11:74353335 | A | ATT | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-1761_556-1760d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353335 | |||||||
| chr11:74353521 | A | C | 3 | a0003c0003t0002g0041 a0003c0003t0002g0082 a0003c0003t0042g0069 |
3 | HG00738.hp1 HG01123.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.556-1945T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353521 | |||||||
| chr11:74353528 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(263): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.556-1952T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353528 | |||||||
| chr11:74353627 | A | G | 2 | a0002c0002t0004g0295 a0002c0002t0004g0302 |
2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.556-2051T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353627 | |||||||
| chr11:74353722 | CCA | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-2148_556-2147d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353722 | |||||||
| chr11:74353790 | C | T | 2 | a0001c0001t0001g0102 a0003c0003t0031g0022 |
2 | NA18959.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.556-2214G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353790 | |||||||
| chr11:74353811 | G | A | 1 | a0002c0002t0054g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.556-2235C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353811 | |||||||
| chr11:74353818 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-2242G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353818 | |||||||
| chr11:74353860 | A | AGACGGGG others(71): Show |
1 | a0001c0001t0003g0230 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.556-2285_556-2284i others(80): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | |||||||
| chr11:74353860 | A | AGACGGGG others(70): Show |
3 | a0004c0005t0014g0182 a0004c0005t0014g0184 a0004c0005t0047g0185 |
3 | HG00642.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.556-2285_556-2284i others(79): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | |||||||
| chr11:74353860 | A | AGACGGGG others(70): Show |
260 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(257): Show |
275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.556-2285_556-2284i others(79): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | |||||||
| chr11:74353860 | A | AGACGGGG others(71): Show |
1 | a0001c0001t0001g0128 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.556-2285_556-2284i others(80): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | |||||||
| chr11:74353860 | A | G | 1 | a0003c0003t0021g0034 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.556-2284T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | |||||||
| chr11:74353863 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(260): Show |
278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.556-2287A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353863 | |||||||
| chr11:74353863 | T | TGGGGTGG others(70): Show |
95 | a0002c0002t0004g0011 a0002c0002t0004g0093 a0002c0002t0004g0100 others(92): Show |
97 | HG00140.hp2 HG00597.hp2 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.556-2288_556-2287i others(79): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353863 | |||||||
| chr11:74353912 | C | T | 1 | a0001c0004t0008g0015 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.556-2336G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353912 | |||||||
| chr11:74354004 | A | G | 1 | a0002c0002t0005g0255 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.556-2428T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354004 | |||||||
| chr11:74354069 | C | T | 1 | a0003c0003t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.556-2493G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354069 | |||||||
| chr11:74354177 | C | T | 1 | a0003c0003t0002g0041 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.556-2601G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354177 | |||||||
| chr11:74354181 | C | T | 1 | a0001c0004t0059g0363 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.556-2605G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354181 | |||||||
| chr11:74354234 | C | A | 14 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(11): Show |
15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-2658G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354234 | |||||||
| chr11:74354366 | G | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-2790C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354366 | |||||||
| chr11:74354367 | T | C | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.556-2791A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354367 | |||||||
| chr11:74354409 | G | A | 2 | a0001c0001t0003g0230 a0001c0001t0003g0311 |
2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.556-2833C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354409 | |||||||
| chr11:74354442 | C | T | 1 | a0002c0002t0005g0298 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.556-2866G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354442 | |||||||
| chr11:74354552 | G | A | 2 | a0002c0002t0004g0100 a0002c0002t0004g0186 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.556-2976C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354552 | |||||||
| chr11:74354725 | C | A | 1 | a0002c0002t0004g0317 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.556-3149G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354725 | |||||||
| chr11:74354806 | G | T | 1 | a0002c0002t0004g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.556-3230C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354806 | |||||||
| chr11:74354874 | G | A | 5 | a0001c0004t0008g0014 a0001c0004t0008g0338 a0001c0004t0008g0339 others(2): Show |
6 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-3298C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354874 | |||||||
| chr11:74355012 | C | T | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-3436G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355012 | |||||||
| chr11:74355063 | G | A | 1 | a0002c0002t0005g0280 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.556-3487C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355063 | |||||||
| chr11:74355080 | G | A | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-3504C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355080 | |||||||
| chr11:74355142 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.556-3566A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355142 | |||||||
| chr11:74355199 | A | G | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.556-3623T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355199 | |||||||
| chr11:74355279 | C | A | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-3703G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355279 | |||||||
| chr11:74355292 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-3716T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355292 | |||||||
| chr11:74355319 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-3743A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355319 | |||||||
| chr11:74355320 | G | A | 1 | a0003c0003t0007g0004 | 2 | NA18977.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.556-3744C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355320 | |||||||
| chr11:74355382 | G | A | 78 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(75): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.556-3806C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355382 | |||||||
| chr11:74355425 | T | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(237): Show |
254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.556-3849A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355425 | |||||||
| chr11:74355427 | G | A | 6 | a0001c0004t0017g0356 a0001c0004t0017g0357 a0001c0004t0017g0360 others(3): Show |
6 | HG01099.hp1 HG01243.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-3851C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355427 | |||||||
| chr11:74355456 | A | AG | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-3881dupC | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355456 | |||||||
| chr11:74355471 | G | A | 3 | a0001c0001t0003g0265 a0001c0001t0003g0328 a0001c0004t0023g0178 |
3 | HG00639.hp2 HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.556-3895C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355471 | |||||||
| chr11:74355479 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-3903C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355479 | |||||||
| chr11:74355486 | G | A | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-3910C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355486 | |||||||
| chr11:74355503 | G | A | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.556-3927C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355503 | |||||||
| chr11:74355541 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-3965C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355541 | |||||||
| chr11:74355553 | C | CA | 20 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0002c0002t0004g0093 others(17): Show |
20 | HG00741.hp2 HG01361.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.556-3978dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(3): Show |
25 | a0001c0001t0003g0209 a0001c0001t0003g0216 a0001c0001t0003g0219 others(22): Show |
25 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.556-3987_556-3978d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(4): Show |
20 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0203 others(17): Show |
20 | HG00544.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.556-3988_556-3978d others(13): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(5): Show |
41 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(38): Show |
43 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.556-3989_556-3978d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(6): Show |
25 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0118 others(22): Show |
25 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.556-3990_556-3978d others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0109 a0001c0001t0001g0121 a0001c0001t0001g0139 others(1): Show |
4 | HG00423.hp2 HG02129.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-3991_556-3978d others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0122 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.556-3994_556-3978d others(19): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(12): Show |
1 | a0004c0005t0014g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.556-3996_556-3978d others(21): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(13): Show |
3 | a0001c0004t0015g0095 a0004c0005t0014g0182 a0004c0005t0014g0184 |
3 | HG03209.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.556-3997_556-3978d others(22): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(14): Show |
1 | a0004c0005t0047g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.556-3998_556-3978d others(23): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(16): Show |
1 | a0004c0005t0050g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.556-4000_556-3978d others(25): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(17): Show |
1 | a0001c0004t0015g0096 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.556-4001_556-3978d others(26): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | C | CAAAAAAA others(18): Show |
1 | a0001c0004t0015g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.556-4002_556-3978d others(27): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | CAA | C | 23 | a0001c0004t0009g0160 a0001c0004t0009g0162 a0001c0004t0009g0163 others(20): Show |
23 | HG00639.hp2 HG02109.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.556-3979_556-3978d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | CAAA | C | 18 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(15): Show |
21 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.556-3980_556-3978d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355553 | CAAAA | C | 11 | a0001c0004t0010g0010 a0001c0004t0017g0356 a0001c0004t0017g0357 others(8): Show |
12 | HG01074.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.556-3981_556-3978d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | |||||||
| chr11:74355569 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0002g0189 a0003c0003t0002g0057 |
2 | HG00558.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.556-4004_556-3994d others(13): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355569 | |||||||
| chr11:74355570 | AAAAAAAA others(3): Show |
A | 76 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(73): Show |
85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.556-4004_556-3995d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355570 | |||||||
| chr11:74355605 | T | C | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-4029A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355605 | |||||||
| chr11:74355635 | G | A | 5 | a0003c0003t0002g0032 a0003c0003t0002g0039 a0003c0003t0002g0051 others(2): Show |
5 | HG00673.hp2 NA18978.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-4059C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355635 | |||||||
| chr11:74355730 | T | C | 14 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(11): Show |
15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-4154A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355730 | |||||||
| chr11:74356106 | G | A | 1 | a0001c0004t0013g0336 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.556-4530C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356106 | |||||||
| chr11:74356120 | C | T | 1 | a0005c0007t0005g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.556-4544G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356120 | |||||||
| chr11:74356144 | G | C | 1 | a0001c0001t0003g0304 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.556-4568C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356144 | |||||||
| chr11:74356301 | G | A | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-4725C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356301 | |||||||
| chr11:74356418 | A | C | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-4842T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356418 | |||||||
| chr11:74356529 | C | T | 7 | a0003c0003t0002g0031 a0003c0003t0002g0032 a0003c0003t0002g0039 others(4): Show |
7 | HG00544.hp1 HG00673.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-4953G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356529 | |||||||
| chr11:74356814 | T | C | 1 | a0003c0003t0002g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.556-5238A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356814 | |||||||
| chr11:74356815 | A | G | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-5239T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356815 | |||||||
| chr11:74356839 | CT | C | 80 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(77): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.556-5264delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356839 | |||||||
| chr11:74356937 | G | A | 80 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(77): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.556-5361C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356937 | |||||||
| chr11:74357095 | C | T | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-5519G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357095 | |||||||
| chr11:74357298 | C | T | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-5722G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357298 | |||||||
| chr11:74357469 | CAAT | C | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.556-5896_556-5894d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357469 | |||||||
| chr11:74357498 | A | G | 6 | a0001c0001t0003g0222 a0001c0001t0003g0242 a0001c0001t0003g0256 others(3): Show |
6 | HG00323.hp1 HG04184.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-5922T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357498 | |||||||
| chr11:74357698 | C | G | 78 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(75): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.556-6122G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357698 | |||||||
| chr11:74357722 | C | T | 8 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(5): Show |
9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-6146G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357722 | |||||||
| chr11:74357748 | A | G | 14 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(11): Show |
15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-6172T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357748 | |||||||
| chr11:74357767 | AG | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.556-6192delC | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357767 | |||||||
| chr11:74357874 | T | A | 1 | a0001c0004t0023g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.556-6298A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357874 | |||||||
| chr11:74357899 | C | T | 2 | a0003c0003t0002g0057 a0003c0003t0002g0084 |
2 | NA18970.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.556-6323G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357899 | |||||||
| chr11:74357926 | A | G | 2 | a0003c0003t0007g0018 a0003c0003t0007g0023 |
2 | HG02523.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.556-6350T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357926 | |||||||
| chr11:74357966 | C | T | 1 | a0001c0001t0036g0227 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.556-6390G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357966 | |||||||
| chr11:74358061 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.556-6485T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358061 | |||||||
| chr11:74358072 | G | C | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-6496C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358072 | |||||||
| chr11:74358576 | T | A | 2 | a0001c0004t0025g0343 a0007c0010t0025g0344 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.556-7000A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358576 | |||||||
| chr11:74358607 | C | T | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-7031G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358607 | |||||||
| chr11:74358653 | C | T | 2 | a0001c0001t0001g0128 a0003c0003t0001g0088 |
2 | NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.556-7077G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358653 | |||||||
| chr11:74358950 | A | G | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-7374T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358950 | |||||||
| chr11:74359056 | A | T | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-7480T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359056 | |||||||
| chr11:74359149 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0039g0117 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.556-7573A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359149 | |||||||
| chr11:74359315 | T | C | 1 | a0002c0002t0005g0286 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.556-7739A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359315 | |||||||
| chr11:74359416 | A | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(221): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.556-7840T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359416 | |||||||
| chr11:74359434 | T | TAC | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-7860_556-7859d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359434 | |||||||
| chr11:74359450 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.556-7874A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359450 | |||||||
| chr11:74359564 | C | CAT | 4 | a0001c0004t0049g0153 a0002c0002t0005g0123 a0002c0002t0005g0147 others(1): Show |
4 | HG02602.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-7990_556-7989d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359564 | |||||||
| chr11:74359564 | C | CATATAT | 24 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(21): Show |
24 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.556-7994_556-7989d others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359564 | |||||||
| chr11:74359564 | CAT | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(202): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.556-7990_556-7989d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359564 | |||||||
| chr11:74359582 | C | T | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-8006G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359582 | |||||||
| chr11:74359689 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0133 |
2 | NA18991.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.556-8113T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359689 | |||||||
| chr11:74359753 | A | G | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-8177T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359753 | |||||||
| chr11:74359756 | T | TGTGGACT others(1): Show |
8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-8188_556-8181d others(10): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359756 | |||||||
| chr11:74359854 | T | A | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.556-8278A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359854 | |||||||
| chr11:74359968 | C | T | 1 | a0001c0001t0011g0305 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.556-8392G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359968 | |||||||
| chr11:74360027 | A | G | 78 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(75): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.556-8451T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360027 | |||||||
| chr11:74360143 | T | C | 1 | a0004c0005t0047g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.555+8349A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360143 | |||||||
| chr11:74360165 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(263): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.555+8327T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360165 | |||||||
| chr11:74360272 | A | AGAAG | 265 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(262): Show |
280 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.555+8216_555+8219d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360272 | |||||||
| chr11:74360379 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0003c0003t0001g0088 |
3 | NA18942.hp2 NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.555+8113G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360379 | |||||||
| chr11:74360524 | C | T | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7968G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360524 | |||||||
| chr11:74360532 | T | A | 1 | a0001c0004t0060g0362 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.555+7960A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360532 | |||||||
| chr11:74360583 | C | T | 4 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+7909G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360583 | |||||||
| chr11:74360610 | A | G | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7882T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360610 | |||||||
| chr11:74360628 | C | T | 1 | a0002c0002t0005g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.555+7864G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360628 | |||||||
| chr11:74360640 | T | C | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+7852A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360640 | |||||||
| chr11:74360680 | G | A | 80 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(77): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.555+7812C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360680 | |||||||
| chr11:74360711 | G | A | 1 | a0001c0001t0011g0308 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.555+7781C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360711 | |||||||
| chr11:74360762 | C | A | 9 | a0001c0001t0041g0188 a0003c0003t0040g0025 a0004c0005t0014g0180 others(6): Show |
9 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+7730G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360762 | |||||||
| chr11:74360847 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.555+7645G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360847 | |||||||
| chr11:74360848 | G | A | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+7644C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360848 | |||||||
| chr11:74360855 | G | C | 1 | a0003c0003t0002g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.555+7637C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360855 | |||||||
| chr11:74360900 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.555+7592C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360900 | |||||||
| chr11:74360995 | C | T | 1 | a0001c0004t0060g0362 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.555+7497G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360995 | |||||||
| chr11:74361128 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(263): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.555+7364A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361128 | |||||||
| chr11:74361148 | C | A | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7344G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361148 | |||||||
| chr11:74361212 | C | A | 1 | a0004c0005t0050g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555+7280G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361212 | |||||||
| chr11:74361247 | C | T | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7245G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361247 | |||||||
| chr11:74361255 | T | A | 1 | a0001c0004t0024g0345 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.555+7237A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361255 | |||||||
| chr11:74361288 | G | T | 22 | a0002c0002t0005g0012 a0002c0002t0005g0159 a0002c0002t0005g0217 others(19): Show |
23 | HG00733.hp2 HG02015.hp1 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.555+7204C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361288 | |||||||
| chr11:74361323 | C | T | 3 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 |
3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.555+7169G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361323 | |||||||
| chr11:74361560 | C | G | 12 | a0001c0004t0013g0333 a0001c0004t0013g0335 a0001c0004t0013g0336 others(9): Show |
12 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.555+6932G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361560 | |||||||
| chr11:74361668 | G | A | 1 | a0002c0002t0005g0287 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.555+6824C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361668 | |||||||
| chr11:74361692 | G | A | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+6800C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361692 | |||||||
| chr11:74361726 | A | T | 1 | a0002c0002t0004g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.555+6766T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361726 | |||||||
| chr11:74361772 | T | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(115): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.555+6720A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361772 | |||||||
| chr11:74361774 | G | C | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+6718C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361774 | |||||||
| chr11:74361846 | GA | G | 13 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(10): Show |
13 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.555+6645delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361846 | |||||||
| chr11:74361920 | G | C | 2 | a0003c0003t0002g0041 a0003c0003t0042g0069 |
2 | HG00738.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.555+6572C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361920 | |||||||
| chr11:74362163 | T | C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(308): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.555+6329A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362163 | |||||||
| chr11:74362279 | T | C | 1 | a0001c0004t0015g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555+6213A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362279 | |||||||
| chr11:74362401 | C | T | 1 | a0002c0002t0004g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.555+6091G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362401 | |||||||
| chr11:74362417 | C | T | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+6075G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362417 | |||||||
| chr11:74362442 | T | C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(308): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.555+6050A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362442 | |||||||
| chr11:74362501 | C | T | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.555+5991G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362501 | |||||||
| chr11:74362528 | A | C | 9 | a0003c0003t0002g0005 a0003c0003t0002g0045 a0003c0003t0002g0058 others(6): Show |
10 | NA18948.hp1 NA18950.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.555+5964T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362528 | |||||||
| chr11:74362651 | C | T | 4 | a0001c0001t0002g0099 a0001c0001t0002g0187 a0001c0001t0044g0101 others(1): Show |
6 | HG00280.hp1 HG00733.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+5841G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362651 | |||||||
| chr11:74362751 | A | C | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.555+5741T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362751 | |||||||
| chr11:74362914 | C | G | 2 | a0002c0002t0004g0100 a0002c0002t0004g0186 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.555+5578G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362914 | |||||||
| chr11:74362954 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(233): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.555+5538A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362954 | |||||||
| chr11:74362955 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0039g0117 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.555+5537C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362955 | |||||||
| chr11:74363009 | G | A | 13 | a0001c0004t0013g0333 a0001c0004t0013g0335 a0001c0004t0013g0336 others(10): Show |
13 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.555+5483C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363009 | |||||||
| chr11:74363031 | A | G | 11 | a0001c0004t0013g0333 a0001c0004t0013g0335 a0001c0004t0013g0336 others(8): Show |
11 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+5461T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363031 | |||||||
| chr11:74363141 | G | A | 1 | a0003c0003t0007g0021 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.555+5351C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363141 | |||||||
| chr11:74363161 | G | A | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+5331C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363161 | |||||||
| chr11:74363292 | G | A | 1 | a0001c0001t0041g0188 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.555+5200C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363292 | |||||||
| chr11:74363349 | C | T | 1 | a0001c0001t0003g0328 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.555+5143G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363349 | |||||||
| chr11:74363530 | A | G | 4 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+4962T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363530 | |||||||
| chr11:74363687 | C | A | 1 | a0001c0004t0023g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.555+4805G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363687 | |||||||
| chr11:74363775 | T | C | 13 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.555+4717A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363775 | |||||||
| chr11:74363828 | T | C | 1 | a0001c0001t0003g0230 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.555+4664A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363828 | |||||||
| chr11:74363877 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(208): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.555+4615G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363877 | |||||||
| chr11:74363893 | G | A | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+4599C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363893 | |||||||
| chr11:74363915 | A | G | 9 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(6): Show |
9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+4577T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363915 | |||||||
| chr11:74363965 | A | G | 1 | a0001c0001t0033g0223 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.555+4527T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363965 | |||||||
| chr11:74364146 | C | T | 2 | a0002c0002t0004g0124 a0002c0002t0004g0245 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.555+4346G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364146 | |||||||
| chr11:74364215 | C | T | 11 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(8): Show |
14 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.555+4277G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364215 | |||||||
| chr11:74364305 | A | C | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.555+4187T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364305 | |||||||
| chr11:74364333 | C | T | 9 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.555+4159G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364333 | |||||||
| chr11:74364393 | G | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(115): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.555+4099C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364393 | |||||||
| chr11:74364470 | C | T | 81 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(78): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.555+4022G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364470 | |||||||
| chr11:74364532 | C | T | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+3960G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364532 | |||||||
| chr11:74364539 | G | C | 1 | a0008c0014t0016g0347 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.555+3953C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364539 | |||||||
| chr11:74364696 | T | C | 1 | a0001c0004t0023g0259 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.555+3796A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364696 | |||||||
| chr11:74364703 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.555+3789G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364703 | |||||||
| chr11:74364790 | C | G | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.555+3702G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364790 | |||||||
| chr11:74364805 | A | G | 1 | a0001c0001t0003g0307 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.555+3687T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364805 | |||||||
| chr11:74364858 | A | G | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.555+3634T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364858 | |||||||
| chr11:74364927 | G | A | 3 | a0002c0002t0004g0221 a0002c0002t0004g0241 a0002c0002t0004g0246 |
3 | HG01074.hp2 HG02148.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.555+3565C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364927 | |||||||
| chr11:74365044 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.555+3448A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365044 | |||||||
| chr11:74365106 | A | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.555+3386T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365106 | |||||||
| chr11:74365117 | G | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.555+3375C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365117 | |||||||
| chr11:74365189 | C | T | 1 | a0005c0007t0055g0053 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.555+3303G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365189 | |||||||
| chr11:74365296 | T | C | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+3196A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365296 | |||||||
| chr11:74365323 | A | C | 1 | a0001c0004t0024g0345 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.555+3169T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365323 | |||||||
| chr11:74365388 | T | C | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.555+3104A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365388 | |||||||
| chr11:74365403 | T | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(224): Show |
238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.555+3089A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365403 | |||||||
| chr11:74365412 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.555+3080T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365412 | |||||||
| chr11:74365536 | C | T | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.555+2956G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365536 | |||||||
| chr11:74365915 | A | G | 1 | a0001c0001t0045g0132 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.555+2577T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365915 | |||||||
| chr11:74366015 | T | C | 8 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(5): Show |
9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+2477A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366015 | |||||||
| chr11:74366131 | A | G | 1 | a0001c0001t0022g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.555+2361T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366131 | |||||||
| chr11:74366253 | C | T | 2 | a0002c0002t0005g0277 a0002c0002t0053g0228 |
2 | NA18955.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.555+2239G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366253 | |||||||
| chr11:74366358 | TA | T | 14 | a0001c0001t0001g0098 a0001c0001t0001g0108 a0001c0001t0001g0131 others(11): Show |
14 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.555+2133delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366358 | |||||||
| chr11:74366459 | T | TA | 25 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(22): Show |
25 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.555+2032dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366459 | |||||||
| chr11:74366459 | TA | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(197): Show |
211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.555+2032delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366459 | |||||||
| chr11:74366464 | A | T | 1 | a0001c0004t0046g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555+2028T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366464 | |||||||
| chr11:74366514 | A | G | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.555+1978T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366514 | |||||||
| chr11:74366699 | T | A | 16 | a0002c0002t0004g0011 a0002c0002t0004g0093 a0002c0002t0004g0100 others(13): Show |
17 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.555+1793A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366699 | |||||||
| chr11:74367050 | A | C | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+1442T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367050 | |||||||
| chr11:74367056 | A | T | 9 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(6): Show |
9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+1436T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367056 | |||||||
| chr11:74367086 | T | C | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.555+1406A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367086 | |||||||
| chr11:74367108 | A | G | 5 | a0001c0001t0003g0219 a0001c0001t0003g0226 a0001c0001t0003g0247 others(2): Show |
5 | NA18944.hp2 NA18956.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+1384T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367108 | |||||||
| chr11:74367244 | G | A | 1 | a0002c0002t0004g0297 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.555+1248C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367244 | |||||||
| chr11:74367317 | T | G | 1 | a0001c0004t0019g0103 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.555+1175A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367317 | |||||||
| chr11:74367338 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.555+1154C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367338 | |||||||
| chr11:74367350 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.555+1142G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367350 | |||||||
| chr11:74367830 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(233): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.555+662C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367830 | |||||||
| chr11:74368108 | C | A | 14 | a0002c0002t0004g0011 a0002c0002t0004g0093 a0002c0002t0004g0170 others(11): Show |
15 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.555+384G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368108 | |||||||
| chr11:74368231 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.555+261C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368231 | |||||||
| chr11:74368430 | A | G | 83 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(80): Show |
92 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.555+62T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368430 | |||||||
| chr11:74368455 | C | T | 1 | a0002c0002t0005g0288 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.555+37G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368455 | |||||||
| chr11:74368626 | C | T | 1 | a0001c0004t0046g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.472-51G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368626 | |||||||
| chr11:74368709 | T | C | 1 | a0002c0002t0005g0292 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.472-134A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368709 | |||||||
| chr11:74368794 | A | T | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.472-219T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368794 | |||||||
| chr11:74368873 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.472-298T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368873 | |||||||
| chr11:74368952 | TC | T | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-378delG | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368952 | |||||||
| chr11:74369032 | G | A | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.472-457C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369032 | |||||||
| chr11:74369062 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(233): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.472-487C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369062 | |||||||
| chr11:74369077 | A | G | 2 | a0003c0003t0002g0057 a0003c0003t0002g0084 |
2 | NA18970.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.472-502T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369077 | |||||||
| chr11:74369191 | A | T | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-616T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369191 | |||||||
| chr11:74369212 | G | A | 4 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-637C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369212 | |||||||
| chr11:74369221 | A | G | 1 | a0001c0004t0060g0362 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.472-646T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369221 | |||||||
| chr11:74369231 | CAT | C | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-658_472-657del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369231 | |||||||
| chr11:74369265 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.472-690A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369265 | |||||||
| chr11:74369319 | C | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.472-744G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369319 | |||||||
| chr11:74369366 | GAAATTTG others(31): Show |
G | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-829_472-792del others(38): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369366 | |||||||
| chr11:74369687 | G | A | 1 | a0003c0003t0002g0074 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.472-1112C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369687 | |||||||
| chr11:74369753 | T | A | 9 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.471+1149A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369753 | |||||||
| chr11:74369804 | C | T | 5 | a0002c0002t0005g0249 a0002c0002t0005g0250 a0002c0002t0005g0251 others(2): Show |
5 | NA18945.hp2 NA18962.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+1098G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369804 | |||||||
| chr11:74369805 | G | A | 1 | a0001c0004t0008g0015 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.471+1097C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369805 | |||||||
| chr11:74369864 | A | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(198): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.471+1038T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369864 | |||||||
| chr11:74369898 | C | T | 2 | a0001c0001t0003g0242 a0001c0001t0003g0268 |
2 | NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.471+1004G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369898 | |||||||
| chr11:74369943 | C | T | 1 | a0009c0011t0026g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.471+959G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369943 | |||||||
| chr11:74370049 | C | A | 1 | a0003c0003t0038g0050 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.471+853G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370049 | |||||||
| chr11:74370066 | C | G | 11 | a0002c0002t0004g0011 a0002c0002t0004g0190 a0002c0002t0004g0191 others(8): Show |
12 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+836G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370066 | |||||||
| chr11:74370105 | G | A | 1 | a0001c0004t0008g0015 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.471+797C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370105 | |||||||
| chr11:74370456 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.471+446C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370456 | |||||||
| chr11:74370470 | G | A | 18 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(15): Show |
19 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+432C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370470 | |||||||
| chr11:74370605 | G | A | 1 | a0001c0001t0022g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.471+297C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370605 | |||||||
| chr11:74371566 | T | G | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.386+145A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371566 | |||||||
| chr11:74371659 | A | C | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+52T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371659 | |||||||
| chr11:74371681 | A | G | 9 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+30T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371681 | |||||||
| chr11:74371703 | C | T | 12 | a0003c0003t0002g0031 a0003c0003t0002g0032 a0003c0003t0002g0035 others(9): Show |
12 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.386+8G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371703 | |||||||
| chr11:74371834 | C | G | 2 | a0001c0004t0008g0340 a0001c0004t0008g0342 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.280-17G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74371834 | |||||||
| chr11:74372043 | C | T | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-226G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372043 | |||||||
| chr11:74372130 | TA | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(241): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.280-314delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372130 | |||||||
| chr11:74372304 | T | C | 2 | a0001c0004t0025g0343 a0007c0010t0025g0344 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.280-487A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372304 | |||||||
| chr11:74372503 | TA | T | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.280-687delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372503 | |||||||
| chr11:74372658 | TA | T | 14 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(11): Show |
15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-842delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372658 | |||||||
| chr11:74372722 | T | G | 37 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(34): Show |
40 | HG00639.hp2 HG01074.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.280-905A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372722 | |||||||
| chr11:74372833 | C | T | 16 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(13): Show |
16 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-1016G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372833 | |||||||
| chr11:74373025 | T | TA | 130 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(127): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.280-1209dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373025 | |||||||
| chr11:74373174 | C | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(127): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.279+1241G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373174 | |||||||
| chr11:74373532 | T | A | 2 | a0001c0004t0026g0213 a0009c0011t0026g0214 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.279+883A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373532 | |||||||
| chr11:74373657 | A | G | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.279+758T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373657 | |||||||
| chr11:74373684 | G | A | 248 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(245): Show |
262 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.279+731C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373684 | |||||||
| chr11:74373829 | A | G | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279+586T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373829 | |||||||
| chr11:74373926 | T | C | 11 | a0002c0002t0004g0011 a0002c0002t0004g0190 a0002c0002t0004g0191 others(8): Show |
12 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+489A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373926 | |||||||
| chr11:74373956 | T | C | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.279+459A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373956 | |||||||
| chr11:74374052 | C | CA | 45 | a0001c0001t0001g0119 a0001c0001t0003g0215 a0001c0001t0039g0117 others(42): Show |
48 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.279+362dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374052 | |||||||
| chr11:74374052 | C | CAA | 108 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(105): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.279+361_279+362dup others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374052 | |||||||
| chr11:74374052 | CA | C | 13 | a0001c0004t0010g0010 a0001c0004t0010g0174 a0001c0004t0015g0094 others(10): Show |
14 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+362delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374052 | |||||||
| chr11:74374071 | AAC | A | 71 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(68): Show |
79 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.279+342_279+343del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374071 | |||||||
| chr11:74374072 | AC | A | 7 | a0001c0001t0022g0354 a0003c0003t0002g0039 a0003c0003t0002g0059 others(4): Show |
7 | HG00673.hp2 HG02615.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+342delG | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374072 | |||||||
| chr11:74374073 | C | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(130): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.279+342G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374073 | |||||||
| chr11:74374146 | C | T | 2 | a0001c0004t0026g0213 a0009c0011t0026g0214 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.279+269G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374146 | |||||||
| chr11:74374166 | C | T | 9 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(6): Show |
9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+249G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374166 | |||||||
| chr11:74374272 | C | CGGGG | 32 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(29): Show |
34 | HG00544.hp2 HG00621.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.279+139_279+142dup others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374272 | |||||||
| chr11:74374339 | C | T | 78 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(75): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.279+76G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374339 | |||||||
| chr11:74374375 | T | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(210): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.279+40A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374375 | |||||||
| chr11:74374596 | G | A | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.112-14C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74374596 | |||||||
| chr11:74374796 | A | C | 1 | a0003c0003t0003g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.112-214T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74374796 | |||||||
| chr11:74374889 | A | G | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-307T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74374889 | |||||||
| chr11:74375004 | G | A | 2 | a0002c0002t0005g0332 a0002c0002t0051g0324 |
2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.112-422C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375004 | |||||||
| chr11:74375063 | G | A | 3 | a0001c0004t0009g0163 a0001c0004t0009g0164 a0001c0004t0009g0167 |
3 | HG02922.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.112-481C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375063 | |||||||
| chr11:74375071 | C | T | 3 | a0002c0002t0004g0093 a0002c0002t0004g0170 a0002c0002t0004g0177 |
3 | HG02055.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.112-489G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375071 | |||||||
| chr11:74375152 | G | A | 1 | a0003c0003t0012g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.112-570C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375152 | |||||||
| chr11:74375172 | C | T | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-590G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375172 | |||||||
| chr11:74375263 | T | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(266): Show |
284 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.112-681A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375263 | |||||||
| chr11:74375315 | A | G | 1 | a0004c0005t0050g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.112-733T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375315 | |||||||
| chr11:74375597 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(210): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.112-1015A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375597 | |||||||
| chr11:74375740 | A | C | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112-1158T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375740 | |||||||
| chr11:74375837 | A | G | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-1255T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375837 | |||||||
| chr11:74376108 | C | G | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-1526G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376108 | |||||||
| chr11:74376203 | A | G | 4 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(1): Show |
4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-1621T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376203 | |||||||
| chr11:74376234 | C | T | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-1652G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376234 | |||||||
| chr11:74376459 | ATATATAT others(6): Show |
A | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-1890_112-1878d others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376459 | |||||||
| chr11:74376548 | T | C | 2 | a0002c0002t0004g0093 a0002c0002t0004g0170 |
2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.112-1966A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376548 | |||||||
| chr11:74376551 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.112-1969T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376551 | |||||||
| chr11:74376579 | T | G | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-1997A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376579 | |||||||
| chr11:74376655 | A | G | 2 | a0002c0002t0027g0278 a0002c0002t0027g0279 |
2 | NA18954.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.112-2073T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376655 | |||||||
| chr11:74376740 | A | C | 6 | a0003c0003t0007g0003 a0003c0003t0007g0004 a0003c0003t0007g0017 others(3): Show |
8 | NA18977.hp2 NA18983.hp1 NA19005.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-2158T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376740 | |||||||
| chr11:74376771 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112-2189A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376771 | |||||||
| chr11:74376989 | T | C | 2 | a0001c0001t0041g0188 a0003c0003t0040g0025 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.112-2407A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376989 | |||||||
| chr11:74377138 | C | CT | 88 | a0001c0001t0001g0210 a0001c0001t0002g0099 a0001c0001t0002g0107 others(85): Show |
97 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.112-2557dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377138 | |||||||
| chr11:74377228 | G | A | 1 | a0001c0001t0003g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.112-2646C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377228 | |||||||
| chr11:74377278 | C | T | 3 | a0003c0003t0002g0041 a0003c0003t0002g0082 a0003c0003t0042g0069 |
3 | HG00738.hp1 HG01123.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.112-2696G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377278 | |||||||
| chr11:74377282 | C | A | 80 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(77): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.112-2700G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377282 | |||||||
| chr11:74377369 | A | G | 1 | a0003c0003t0002g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.112-2787T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377369 | |||||||
| chr11:74377496 | G | T | 83 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(80): Show |
92 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-2914C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377496 | |||||||
| chr11:74377611 | G | C | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-3029C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377611 | |||||||
| chr11:74377698 | C | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(262): Show |
280 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.112-3116G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377698 | |||||||
| chr11:74377947 | G | GA | 7 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-3366dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377947 | |||||||
| chr11:74378068 | G | A | 1 | a0003c0003t0003g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.112-3486C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378068 | |||||||
| chr11:74378650 | T | C | 26 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(23): Show |
26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-4068A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378650 | |||||||
| chr11:74378680 | G | A | 10 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(7): Show |
13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-4098C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378680 | |||||||
| chr11:74378692 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112-4110T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378692 | |||||||
| chr11:74378771 | T | C | 1 | a0008c0014t0016g0347 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.112-4189A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378771 | |||||||
| chr11:74378853 | C | T | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.112-4271G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378853 | |||||||
| chr11:74379024 | C | T | 36 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(33): Show |
39 | HG00639.hp2 HG01884.hp1 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.112-4442G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379024 | |||||||
| chr11:74379181 | T | C | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-4599A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379181 | |||||||
| chr11:74379188 | C | T | 2 | a0002c0002t0005g0277 a0002c0002t0053g0228 |
2 | NA18955.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.112-4606G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379188 | |||||||
| chr11:74379294 | C | T | 80 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(77): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.112-4712G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379294 | |||||||
| chr11:74379651 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.112-5069G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379651 | |||||||
| chr11:74379817 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.112-5235G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379817 | |||||||
| chr11:74379883 | A | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(262): Show |
280 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.112-5301T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379883 | |||||||
| chr11:74380003 | A | G | 9 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-5421T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380003 | |||||||
| chr11:74380027 | T | C | 1 | a0002c0002t0004g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.112-5445A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380027 | |||||||
| chr11:74380201 | C | A | 2 | a0002c0002t0005g0123 a0002c0002t0005g0149 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.112-5619G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380201 | |||||||
| chr11:74380292 | T | G | 29 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(26): Show |
29 | HG00639.hp2 HG01074.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.112-5710A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380292 | |||||||
| chr11:74380367 | TTTCC | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(205): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.112-5789_112-5786d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380367 | |||||||
| chr11:74380412 | T | C | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-5830A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380412 | |||||||
| chr11:74380464 | T | C | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-5882A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380464 | |||||||
| chr11:74380497 | GATTT | G | 3 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 |
3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112-5919_112-5916d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380497 | |||||||
| chr11:74380678 | T | A | 80 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(77): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.112-6096A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380678 | |||||||
| chr11:74380754 | C | G | 3 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 |
3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112-6172G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380754 | |||||||
| chr11:74380777 | A | G | 2 | a0001c0004t0009g0165 a0001c0004t0009g0166 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.112-6195T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380777 | |||||||
| chr11:74380909 | C | T | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-6327G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380909 | |||||||
| chr11:74381139 | A | G | 2 | a0001c0001t0003g0231 a0001c0001t0003g0304 |
2 | HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.112-6557T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381139 | |||||||
| chr11:74381177 | C | T | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-6595G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381177 | |||||||
| chr11:74381358 | T | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(205): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.112-6776A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381358 | |||||||
| chr11:74381361 | A | G | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-6779T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381361 | |||||||
| chr11:74381420 | A | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(208): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.112-6838T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381420 | |||||||
| chr11:74381515 | T | C | 1 | a0001c0013t0032g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-6933A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381515 | |||||||
| chr11:74381571 | C | CT | 18 | a0001c0001t0001g0148 a0001c0004t0015g0094 a0001c0004t0015g0095 others(15): Show |
18 | HG01081.hp1 HG01884.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.112-6990dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | |||||||
| chr11:74381571 | CT | C | 38 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(35): Show |
43 | HG01099.hp1 HG01099.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.112-6990delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | |||||||
| chr11:74381571 | CTTT | C | 95 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(92): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.112-6992_112-6990d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | |||||||
| chr11:74381571 | CTTTT | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.112-6993_112-6990d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | |||||||
| chr11:74381576 | T | C | 2 | a0003c0003t0006g0072 a0003c0003t0007g0019 |
2 | HG01175.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.112-6994A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381576 | |||||||
| chr11:74381577 | T | C | 78 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(75): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.112-6995A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381577 | |||||||
| chr11:74381663 | G | A | 1 | a0003c0006t0048g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112-7081C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381663 | |||||||
| chr11:74381889 | C | G | 5 | a0002c0002t0004g0236 a0002c0002t0004g0238 a0002c0002t0004g0239 others(2): Show |
5 | NA18998.hp2 NA19062.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-7307G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381889 | |||||||
| chr11:74381901 | TC | T | 10 | a0002c0002t0004g0220 a0002c0002t0004g0236 a0002c0002t0004g0238 others(7): Show |
10 | HG02027.hp2 NA18950.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-7320delG | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381901 | |||||||
| chr11:74381902 | C | T | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.112-7320G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381902 | |||||||
| chr11:74381906 | C | A | 1 | a0002c0002t0004g0314 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.112-7324G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381906 | |||||||
| chr11:74381911 | C | G | 1 | a0001c0004t0024g0345 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112-7329G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381911 | |||||||
| chr11:74382108 | G | A | 2 | a0002c0002t0005g0332 a0002c0002t0051g0324 |
2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.112-7526C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382108 | |||||||
| chr11:74382140 | G | A | 3 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 |
3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112-7558C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382140 | |||||||
| chr11:74382176 | G | A | 10 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(7): Show |
13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-7594C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382176 | |||||||
| chr11:74382216 | T | C | 2 | a0003c0003t0002g0039 a0003c0003t0002g0051 |
2 | HG00673.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.112-7634A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382216 | |||||||
| chr11:74382223 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(112): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.112-7641C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382223 | |||||||
| chr11:74382365 | G | A | 3 | a0001c0004t0016g0348 a0001c0004t0016g0349 a0008c0014t0016g0347 |
3 | HG02723.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.112-7783C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382365 | |||||||
| chr11:74382453 | C | T | 3 | a0002c0002t0004g0248 a0002c0002t0004g0296 a0002c0002t0054g0325 |
3 | HG01361.hp1 HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.112-7871G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382453 | |||||||
| chr11:74382947 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(209): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.112-8365G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382947 | |||||||
| chr11:74383085 | C | T | 1 | a0009c0011t0026g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.112-8503G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383085 | |||||||
| chr11:74383093 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(209): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.112-8511A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383093 | |||||||
| chr11:74383298 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0098 others(209): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.112-8716T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383298 | |||||||
| chr11:74383408 | G | A | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-8826C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383408 | |||||||
| chr11:74383453 | T | G | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-8871A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383453 | |||||||
| chr11:74383693 | C | T | 5 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-9111G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383693 | |||||||
| chr11:74383820 | A | AATATATA others(21): Show |
1 | a0002c0002t0004g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.112-9239_112-9238i others(30): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383820 | |||||||
| chr11:74383820 | A | AATATATA others(23): Show |
1 | a0002c0002t0004g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112-9239_112-9238i others(32): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383820 | |||||||
| chr11:74383824 | A | AAT | 102 | a0001c0001t0002g0099 a0001c0001t0002g0107 a0001c0001t0002g0126 others(99): Show |
111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.112-9244_112-9243d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(31): Show |
1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-9243_112-9242i others(40): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(7): Show |
2 | a0001c0004t0009g0165 a0001c0004t0009g0166 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(25): Show |
5 | a0002c0002t0004g0192 a0002c0002t0004g0193 a0002c0002t0004g0194 others(2): Show |
5 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(34): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(27): Show |
4 | a0001c0004t0049g0153 a0002c0002t0004g0011 a0002c0002t0004g0191 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(36): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(26): Show |
1 | a0002c0002t0004g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(35): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(7): Show |
14 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(11): Show |
14 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(9): Show |
1 | a0001c0001t0003g0276 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(18): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(11): Show |
3 | a0001c0001t0003g0260 a0001c0001t0022g0353 a0001c0004t0023g0178 |
3 | HG00639.hp2 HG02622.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(20): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(17): Show |
1 | a0009c0011t0026g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(26): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(19): Show |
3 | a0001c0004t0025g0343 a0003c0006t0015g0026 a0007c0010t0025g0344 |
3 | HG02572.hp1 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(28): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(21): Show |
1 | a0001c0004t0026g0213 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(30): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(23): Show |
1 | a0002c0002t0004g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.112-9243_112-9242i others(32): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATAAATA others(27): Show |
1 | a0002c0002t0004g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(36): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(1): Show |
10 | a0001c0001t0003g0293 a0001c0001t0022g0354 a0001c0004t0008g0013 others(7): Show |
13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-9250_112-9243d others(10): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(3): Show |
30 | a0001c0001t0003g0219 a0002c0002t0005g0012 a0002c0002t0005g0158 others(27): Show |
31 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.112-9252_112-9243d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(5): Show |
43 | a0001c0001t0001g0273 a0001c0001t0003g0230 a0001c0001t0003g0231 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.112-9254_112-9243d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(7): Show |
15 | a0001c0001t0003g0216 a0001c0001t0003g0256 a0001c0001t0003g0257 others(12): Show |
15 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-9256_112-9243d others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(9): Show |
13 | a0001c0001t0003g0215 a0001c0001t0003g0222 a0001c0001t0003g0226 others(10): Show |
13 | HG01069.hp2 HG02027.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-9258_112-9243d others(18): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(11): Show |
4 | a0001c0001t0003g0234 a0001c0004t0013g0337 a0002c0002t0004g0236 others(1): Show |
4 | HG02630.hp2 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-9260_112-9243d others(20): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(13): Show |
7 | a0001c0001t0011g0331 a0002c0002t0004g0243 a0002c0002t0004g0321 others(4): Show |
7 | HG01517.hp1 HG02004.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(22): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(15): Show |
6 | a0001c0001t0003g0235 a0002c0002t0004g0303 a0002c0002t0005g0253 others(3): Show |
6 | NA18747.hp2 NA18962.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(24): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(17): Show |
6 | a0001c0004t0024g0345 a0002c0002t0004g0299 a0002c0002t0004g0300 others(3): Show |
6 | HG01516.hp1 HG02559.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(26): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(19): Show |
5 | a0001c0004t0013g0336 a0002c0002t0004g0297 a0002c0002t0005g0250 others(2): Show |
5 | HG01081.hp1 HG02258.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(28): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(21): Show |
3 | a0001c0004t0013g0335 a0002c0002t0004g0233 a0002c0002t0004g0317 |
3 | HG03195.hp2 NA18953.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(30): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(23): Show |
2 | a0001c0004t0015g0096 a0002c0002t0054g0325 |
2 | HG01361.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(32): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(25): Show |
4 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0002c0002t0004g0296 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(34): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(27): Show |
1 | a0002c0002t0004g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(36): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | AATATATA others(29): Show |
1 | a0002c0002t0004g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-9243_112-9242i others(38): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383824 | A | T | 2 | a0002c0002t0004g0100 a0002c0002t0004g0186 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.112-9242T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | |||||||
| chr11:74383860 | G | C | 1 | a0002c0002t0004g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.112-9278C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383860 | |||||||
| chr11:74383868 | C | T | 1 | a0003c0003t0002g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112-9286G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383868 | |||||||
| chr11:74383869 | C | T | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112-9287G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383869 | |||||||
| chr11:74384138 | C | T | 2 | a0001c0001t0003g0247 a0001c0004t0010g0174 |
2 | HG04228.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.112-9556G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384138 | |||||||
| chr11:74384329 | T | C | 2 | a0002c0002t0004g0100 a0002c0002t0004g0186 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.112-9747A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384329 | |||||||
| chr11:74384333 | T | C | 1 | a0002c0002t0054g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.112-9751A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384333 | |||||||
| chr11:74384394 | T | A | 3 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-9812A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384394 | |||||||
| chr11:74384467 | C | T | 2 | a0001c0001t0001g0128 a0003c0003t0001g0088 |
2 | NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.112-9885G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384467 | |||||||
| chr11:74384505 | G | C | 9 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-9923C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384505 | |||||||
| chr11:74384514 | G | C | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112-9932C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384514 | |||||||
| chr11:74384778 | T | C | 2 | a0003c0003t0002g0008 a0003c0003t0002g0066 |
3 | HG02040.hp1 NA18941.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.112-10196A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384778 | |||||||
| chr11:74384817 | T | C | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-10235A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384817 | |||||||
| chr11:74384908 | C | T | 1 | a0001c0001t0033g0223 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.112-10326G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384908 | |||||||
| chr11:74385089 | T | C | 105 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0107 others(102): Show |
115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.112-10507A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385089 | |||||||
| chr11:74385302 | T | C | 1 | a0001c0004t0046g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.112-10720A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385302 | |||||||
| chr11:74385424 | G | T | 1 | a0001c0001t0022g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112-10842C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385424 | |||||||
| chr11:74385425 | ACAATTTA others(3): Show |
A | 1 | a0001c0001t0022g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112-10853_112-1084 others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385425 | |||||||
| chr11:74385494 | C | A | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-10912G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385494 | |||||||
| chr11:74385549 | T | C | 1 | a0003c0003t0006g0052 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.112-10967A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385549 | |||||||
| chr11:74385633 | A | G | 7 | a0001c0004t0017g0356 a0001c0004t0017g0357 a0001c0004t0017g0360 others(4): Show |
7 | HG01099.hp1 HG01243.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-11051T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385633 | |||||||
| chr11:74385797 | A | T | 11 | a0002c0002t0004g0011 a0002c0002t0004g0190 a0002c0002t0004g0191 others(8): Show |
12 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.112-11215T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385797 | |||||||
| chr11:74385950 | G | C | 295 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(292): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.112-11368C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385950 | |||||||
| chr11:74386002 | G | T | 105 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0107 others(102): Show |
115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.112-11420C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386002 | |||||||
| chr11:74386081 | G | A | 294 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(291): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.112-11499C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386081 | |||||||
| chr11:74386141 | A | G | 184 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(181): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.112-11559T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386141 | |||||||
| chr11:74386170 | A | C | 9 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-11588T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386170 | |||||||
| chr11:74386421 | T | G | 187 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(184): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.111+11630A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386421 | |||||||
| chr11:74386480 | C | CT | 9 | a0001c0001t0001g0118 a0001c0001t0001g0128 a0001c0001t0001g0156 others(6): Show |
9 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+11570dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386480 | |||||||
| chr11:74386920 | G | A | 184 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(181): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.111+11131C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386920 | |||||||
| chr11:74386998 | G | C | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+11053C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386998 | |||||||
| chr11:74387044 | T | C | 9 | a0001c0001t0041g0188 a0001c0004t0008g0013 a0001c0004t0008g0014 others(6): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+11007A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387044 | |||||||
| chr11:74387212 | G | A | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+10839C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387212 | |||||||
| chr11:74387237 | T | C | 25 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(22): Show |
26 | HG00642.hp2 HG01099.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+10814A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387237 | |||||||
| chr11:74387437 | C | T | 105 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0107 others(102): Show |
115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.111+10614G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387437 | |||||||
| chr11:74387600 | G | T | 295 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(292): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.111+10451C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387600 | |||||||
| chr11:74387651 | T | C | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+10400A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387651 | |||||||
| chr11:74387688 | C | T | 146 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(143): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.111+10363G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387688 | |||||||
| chr11:74387793 | T | C | 1 | a0001c0001t0022g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.111+10258A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387793 | |||||||
| chr11:74387849 | G | A | 1 | a0001c0001t0041g0188 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.111+10202C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387849 | |||||||
| chr11:74388305 | C | T | 184 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(181): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.111+9746G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388305 | |||||||
| chr11:74388335 | TA | T | 295 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(292): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.111+9715delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388335 | |||||||
| chr11:74388497 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111+9554G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388497 | |||||||
| chr11:74388516 | A | C | 105 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0107 others(102): Show |
115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.111+9535T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388516 | |||||||
| chr11:74388583 | T | C | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+9468A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388583 | |||||||
| chr11:74388591 | G | A | 184 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(181): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.111+9460C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388591 | |||||||
| chr11:74388652 | T | C | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+9399A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388652 | |||||||
| chr11:74388682 | C | T | 2 | a0002c0002t0004g0100 a0002c0002t0004g0186 |
2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.111+9369G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388682 | |||||||
| chr11:74388785 | T | C | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+9266A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388785 | |||||||
| chr11:74388847 | T | C | 295 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(292): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.111+9204A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388847 | |||||||
| chr11:74389062 | T | A | 5 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0001c0004t0049g0153 others(2): Show |
5 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+8989A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389062 | |||||||
| chr11:74389282 | C | G | 105 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0107 others(102): Show |
115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.111+8769G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389282 | |||||||
| chr11:74389495 | G | A | 184 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(181): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.111+8556C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389495 | |||||||
| chr11:74389601 | T | C | 184 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(181): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.111+8450A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389601 | |||||||
| chr11:74389621 | G | A | 10 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(7): Show |
10 | HG00642.hp2 HG01261.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.111+8430C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389621 | |||||||
| chr11:74389720 | G | C | 4 | a0001c0004t0019g0103 a0001c0004t0019g0104 a0001c0004t0019g0105 others(1): Show |
4 | HG01074.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+8331C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389720 | |||||||
| chr11:74389947 | C | CA | 11 | a0001c0001t0001g0116 a0001c0001t0001g0156 a0001c0001t0001g0200 others(8): Show |
11 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+8103dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAA | 87 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(84): Show |
88 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.111+8099_111+8103d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAA | 62 | a0001c0001t0003g0222 a0001c0001t0003g0230 a0001c0001t0003g0231 others(59): Show |
65 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.111+8098_111+8103d others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA | 9 | a0001c0001t0003g0318 a0001c0001t0003g0319 a0001c0001t0041g0188 others(6): Show |
9 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+8097_111+8103d others(9): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(3): Show |
30 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0152 others(27): Show |
35 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.111+8094_111+8103d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(4): Show |
44 | a0001c0001t0002g0126 a0001c0001t0002g0189 a0001c0004t0017g0357 others(41): Show |
47 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.111+8093_111+8103d others(13): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(5): Show |
15 | a0001c0001t0002g0107 a0001c0004t0010g0010 a0001c0004t0010g0171 others(12): Show |
17 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.111+8092_111+8103d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(6): Show |
8 | a0001c0004t0010g0174 a0001c0004t0010g0175 a0001c0004t0010g0176 others(5): Show |
8 | HG01175.hp1 HG02135.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+8091_111+8103d others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(7): Show |
2 | a0001c0013t0032g0169 a0002c0002t0004g0170 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.111+8090_111+8103d others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(8): Show |
1 | a0004c0005t0014g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.111+8089_111+8103d others(17): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(9): Show |
6 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0004c0005t0014g0181 others(3): Show |
6 | HG01261.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+8088_111+8103d others(18): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | C | CAAAAAAA others(10): Show |
4 | a0001c0004t0016g0349 a0004c0005t0014g0183 a0004c0005t0014g0184 others(1): Show |
4 | HG00642.hp2 HG03492.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+8087_111+8103d others(19): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | CA | C | 5 | a0001c0001t0039g0117 a0002c0002t0004g0011 a0002c0002t0004g0193 others(2): Show |
6 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+8103delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389947 | CAA | C | 8 | a0002c0002t0004g0100 a0002c0002t0004g0186 a0002c0002t0004g0190 others(5): Show |
8 | HG01106.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+8102_111+8103d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | |||||||
| chr11:74389968 | A | AAAAAAAA others(6): Show |
1 | a0003c0003t0002g0082 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.111+8082_111+8083i others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389968 | |||||||
| chr11:74389974 | C | G | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.111+8077G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389974 | |||||||
| chr11:74389976 | A | G | 296 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(293): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.111+8075T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389976 | |||||||
| chr11:74390033 | G | A | 3 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 |
3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.111+8018C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390033 | |||||||
| chr11:74390035 | C | T | 155 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(152): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.111+8016G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390035 | |||||||
| chr11:74390118 | CA | C | 160 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.111+7932delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390118 | |||||||
| chr11:74390118 | CAA | C | 16 | a0001c0001t0003g0242 a0002c0002t0004g0220 a0002c0002t0004g0221 others(13): Show |
16 | HG01074.hp2 HG02027.hp2 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.111+7931_111+7932d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390118 | |||||||
| chr11:74390170 | G | GA | 246 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(243): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.111+7880dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390170 | |||||||
| chr11:74390170 | G | GAA | 35 | a0001c0001t0003g0235 a0001c0001t0035g0320 a0001c0004t0010g0010 others(32): Show |
36 | HG00438.hp2 HG00642.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.111+7879_111+7880d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390170 | |||||||
| chr11:74390372 | C | A | 1 | a0001c0004t0023g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.111+7679G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390372 | |||||||
| chr11:74390752 | A | C | 4 | a0001c0004t0025g0343 a0001c0004t0026g0213 a0007c0010t0025g0344 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+7299T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390752 | |||||||
| chr11:74390941 | G | A | 3 | a0002c0002t0004g0321 a0002c0002t0004g0322 a0002c0002t0004g0323 |
3 | NA18956.hp2 NA18965.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.111+7110C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390941 | |||||||
| chr11:74391176 | C | T | 3 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0002c0002t0004g0233 |
3 | NA18747.hp2 NA18953.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.111+6875G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391176 | |||||||
| chr11:74391274 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(41): Show |
47 | HG00544.hp2 HG00621.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.111+6777G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391274 | |||||||
| chr11:74391333 | T | C | 21 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(18): Show |
22 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.111+6718A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391333 | |||||||
| chr11:74391726 | T | A | 1 | a0002c0002t0051g0324 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111+6325A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391726 | |||||||
| chr11:74391828 | TGGTATG | T | 101 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0187 others(98): Show |
111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.111+6217_111+6222d others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391828 | |||||||
| chr11:74391834 | G | T | 1 | a0001c0004t0058g0355 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.111+6217C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391834 | |||||||
| chr11:74391929 | T | C | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+6122A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391929 | |||||||
| chr11:74392348 | G | A | 1 | a0002c0002t0054g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.111+5703C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392348 | |||||||
| chr11:74392356 | T | G | 1 | a0002c0002t0054g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.111+5695A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392356 | |||||||
| chr11:74392365 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111+5686T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392365 | |||||||
| chr11:74392669 | G | A | 5 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+5382C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392669 | |||||||
| chr11:74392735 | C | T | 187 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(184): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.111+5316G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392735 | |||||||
| chr11:74392791 | C | T | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+5260G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392791 | |||||||
| chr11:74392836 | G | A | 1 | a0001c0004t0017g0361 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111+5215C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392836 | |||||||
| chr11:74393022 | T | C | 145 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(142): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.111+5029A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393022 | |||||||
| chr11:74393043 | T | C | 5 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+5008A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393043 | |||||||
| chr11:74393266 | A | C | 1 | a0003c0003t0002g0005 | 2 | NA18948.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.111+4785T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393266 | |||||||
| chr11:74393328 | C | T | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+4723G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393328 | |||||||
| chr11:74393463 | T | C | 184 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(181): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.111+4588A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393463 | |||||||
| chr11:74393630 | A | G | 1 | a0003c0003t0002g0045 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.111+4421T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393630 | |||||||
| chr11:74393679 | C | A | 1 | a0001c0001t0003g0326 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+4372G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393679 | |||||||
| chr11:74393977 | GA | G | 288 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(285): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.111+4073delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393977 | |||||||
| chr11:74394060 | C | T | 155 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(152): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.111+3991G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394060 | |||||||
| chr11:74394318 | A | G | 8 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(5): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+3733T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394318 | |||||||
| chr11:74394444 | C | T | 1 | a0001c0009t0029g0358 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+3607G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394444 | |||||||
| chr11:74394804 | T | C | 10 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(7): Show |
11 | HG01099.hp2 HG02055.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+3247A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394804 | |||||||
| chr11:74394950 | C | CTA | 290 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(287): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.111+3100_111+3101i others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394950 | |||||||
| chr11:74394954 | T | G | 1 | a0003c0003t0040g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+3097A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394954 | |||||||
| chr11:74395532 | C | T | 1 | a0001c0001t0003g0219 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.111+2519G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395532 | |||||||
| chr11:74395549 | C | CT | 28 | a0001c0001t0001g0097 a0001c0001t0001g0108 a0001c0001t0001g0109 others(25): Show |
28 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.111+2501dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395549 | C | CTT | 6 | a0001c0001t0001g0106 a0001c0001t0001g0200 a0001c0001t0002g0107 others(3): Show |
7 | HG00438.hp1 HG02145.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+2500_111+2501d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395549 | C | CTTT | 64 | a0001c0001t0001g0102 a0001c0001t0002g0189 a0001c0001t0022g0353 others(61): Show |
71 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.111+2499_111+2501d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395549 | C | CTTTT | 31 | a0001c0001t0002g0099 a0001c0001t0002g0187 a0001c0004t0017g0356 others(28): Show |
33 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.111+2498_111+2501d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395549 | CTTT | C | 7 | a0001c0001t0003g0219 a0001c0004t0008g0339 a0001c0004t0016g0346 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+2499_111+2501d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395549 | CTTTT | C | 47 | a0001c0001t0003g0222 a0001c0001t0003g0226 a0001c0001t0003g0230 others(44): Show |
51 | HG00639.hp2 HG00642.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.111+2498_111+2501d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395549 | CTTTTT | C | 127 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(124): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.111+2497_111+2501d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395549 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0003g0326 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+2490_111+2501d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | |||||||
| chr11:74395550 | T | C | 1 | a0001c0004t0049g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.111+2501A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395550 | |||||||
| chr11:74395553 | T | C | 1 | a0002c0002t0004g0170 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.111+2498A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395553 | |||||||
| chr11:74395554 | T | C | 9 | a0001c0004t0010g0010 a0001c0004t0010g0171 a0001c0004t0010g0172 others(6): Show |
10 | HG01099.hp2 HG03209.hp2 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+2497A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395554 | |||||||
| chr11:74395597 | G | A | 7 | a0004c0005t0014g0180 a0004c0005t0014g0181 a0004c0005t0014g0182 others(4): Show |
7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+2454C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395597 | |||||||
| chr11:74395613 | G | A | 9 | a0001c0004t0009g0160 a0001c0004t0009g0161 a0001c0004t0009g0162 others(6): Show |
9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+2438C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395613 | |||||||
| chr11:74395650 | G | A | 11 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(8): Show |
11 | HG00639.hp2 HG00642.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+2401C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395650 | |||||||
| chr11:74395714 | A | G | 12 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(9): Show |
15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+2337T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395714 | |||||||
| chr11:74395793 | C | T | 290 | a0001c0001t0001g0102 a0001c0001t0001g0273 a0001c0001t0002g0099 others(287): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.111+2258G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395793 | |||||||
| chr11:74395810 | C | T | 1 | a0001c0004t0008g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.111+2241G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395810 | |||||||
| chr11:74395973 | C | T | 100 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0187 others(97): Show |
110 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.111+2078G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395973 | |||||||
| chr11:74396025 | G | C | 1 | a0001c0001t0037g0327 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.111+2026C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396025 | |||||||
| chr11:74396086 | T | TA | 7 | a0001c0001t0003g0328 a0001c0004t0016g0346 a0001c0004t0016g0348 others(4): Show |
7 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+1964dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396086 | |||||||
| chr11:74396099 | A | T | 94 | a0001c0001t0001g0102 a0001c0001t0002g0099 a0001c0001t0002g0187 others(91): Show |
103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.111+1952T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396099 | |||||||
| chr11:74396152 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0002g0212 a0001c0001t0003g0154 |
3 | HG01257.hp2 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.111+1899C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396152 | |||||||
| chr11:74396206 | T | A | 1 | a0003c0003t0002g0082 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.111+1845A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396206 | |||||||
| chr11:74396221 | T | C | 2 | a0001c0001t0003g0329 a0001c0001t0003g0330 |
2 | NA18954.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.111+1830A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396221 | |||||||
| chr11:74396266 | T | TA | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0003c0003t0001g0088 others(5): Show |
8 | HG03239.hp2 HG04199.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+1784dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396266 | |||||||
| chr11:74396266 | TAAA | T | 181 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(178): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.111+1782_111+1784d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396266 | |||||||
| chr11:74396359 | G | C | 1 | a0003c0006t0015g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+1692C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396359 | |||||||
| chr11:74396440 | A | T | 1 | a0001c0004t0046g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+1611T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396440 | |||||||
| chr11:74396449 | C | T | 12 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(9): Show |
15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+1602G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396449 | |||||||
| chr11:74396454 | G | A | 12 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(9): Show |
15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+1597C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396454 | |||||||
| chr11:74396484 | C | G | 2 | a0001c0001t0003g0215 a0001c0001t0003g0216 |
2 | HG01069.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.111+1567G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396484 | |||||||
| chr11:74396560 | G | C | 5 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1491C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396560 | |||||||
| chr11:74396609 | T | C | 12 | a0001c0004t0008g0013 a0001c0004t0008g0014 a0001c0004t0008g0015 others(9): Show |
15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+1442A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396609 | |||||||
| chr11:74396706 | G | A | 145 | a0001c0001t0001g0273 a0001c0001t0003g0215 a0001c0001t0003g0216 others(142): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.111+1345C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396706 | |||||||
| chr11:74396710 | G | A | 6 | a0001c0004t0013g0333 a0001c0004t0013g0335 a0001c0004t0013g0336 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1341C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396710 | |||||||
| chr11:74396976 | T | A | 5 | a0001c0004t0016g0346 a0001c0004t0016g0348 a0001c0004t0016g0349 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1075A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396976 | |||||||
| chr11:74396983 | T | C | 1 | a0003c0003t0002g0092 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.111+1068A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396983 | |||||||
| chr11:74397369 | T | C | 16 | a0001c0001t0022g0354 a0001c0004t0008g0013 a0001c0004t0008g0014 others(13): Show |
19 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.111+682A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397369 | |||||||
| chr11:74397526 | C | G | 197 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0200 others(194): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.111+525G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397526 | |||||||
| chr11:74397536 | T | G | 1 | a0001c0004t0046g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+515A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397536 | |||||||
| chr11:74397568 | G | A | 198 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(195): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.111+483C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397568 | |||||||
| chr11:74397586 | A | G | 4 | a0001c0004t0015g0094 a0001c0004t0015g0095 a0001c0004t0015g0096 others(1): Show |
4 | HG01884.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+465T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397586 | |||||||
| chr11:74397734 | C | A | 1 | a0001c0004t0059g0363 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.111+317G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397734 | |||||||
| chr11:74397745 | A | AT | 25 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0001c0001t0002g0107 others(22): Show |
26 | HG00609.hp1 HG01099.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.111+305dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | |||||||
| chr11:74397745 | A | ATT | 79 | a0001c0004t0008g0014 a0001c0004t0008g0015 a0001c0004t0008g0338 others(76): Show |
86 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.111+304_111+305dup others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | |||||||
| chr11:74397745 | A | ATTT | 24 | a0001c0001t0001g0211 a0001c0001t0003g0215 a0001c0001t0003g0328 others(21): Show |
25 | HG00280.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.111+303_111+305dup others(3): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | |||||||
| chr11:74397745 | A | ATTTT | 136 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(133): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.111+302_111+305dup others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | |||||||
| chr11:74397745 | A | ATTTTT | 15 | a0001c0001t0001g0273 a0001c0001t0003g0230 a0001c0001t0003g0266 others(12): Show |
15 | HG00639.hp2 HG01243.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+301_111+305dup others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | |||||||
| chr11:74397745 | A | T | 9 | a0002c0002t0004g0011 a0002c0002t0004g0190 a0002c0002t0004g0191 others(6): Show |
10 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+306T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | |||||||
| chr11:74397745 | AT | A | 6 | a0001c0001t0001g0135 a0001c0001t0022g0354 a0001c0004t0019g0103 others(3): Show |
6 | HG01074.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+305delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | |||||||
| chr11:74397769 | A | G | 1 | a0001c0004t0058g0355 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.111+282T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397769 | |||||||
| chr11:74397905 | G | A | 83 | a0001c0001t0022g0353 a0001c0001t0022g0354 a0003c0003t0001g0080 others(80): Show |
92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.111+146C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397905 |