| geneid | 283659 |
|---|---|
| ensemblid | ENSG00000166450.13 |
| hgncid | 26373 |
| symbol | PRTG |
| name | protogenin |
| refseq_nuc | NM_173814.6 |
| refseq_prot | NP_776175.2 |
| ensembl_nuc | ENST00000389286.9 |
| ensembl_prot | ENSP00000373937.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 55611544 |
| end | 55743152 |
| strand | - |
| ver | v1.2 |
| region | chr15:55611544-55743152 |
| region5000 | chr15:55606544-55748152 |
| regionname0 | PRTG_chr15_55611544_55743152 |
| regionname5000 | PRTG_chr15_55606544_55748152 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1150 | 181 | 44 | 47 | 53 | 7 | 28 | 41 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002 | 0/0 | 1150 | 65 | 22 | 10 | 26 | 1 | 6 | 22 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003 | 0/0 | 1150 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004 | 0/0 | 1150 | 11 | 0 | 5 | 0 | 5 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0005 | 0/0 | 1150 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0006 | 0/0 | 1150 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0007 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0008 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0009 | 0/0 | 1150 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0010 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0011 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0012 | 0/0 | 1150 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0013 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0014 | 0/0 | 1150 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0015 | 0/0 | 1150 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0016 | 0/0 | 1150 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3453 | 154 | 29 | 43 | 46 | 6 | 28 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0002 | 0/0 | 3453 | 65 | 22 | 10 | 26 | 1 | 6 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0003 | 0/0 | 3453 | 11 | 0 | 3 | 7 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0004 | 0/0 | 3453 | 11 | 10 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0005 | 0/0 | 3453 | 6 | 0 | 3 | 0 | 2 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0006 | 0/0 | 3453 | 5 | 0 | 2 | 0 | 3 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0007 | 0/0 | 3453 | 5 | 5 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0008 | 0/0 | 3453 | 4 | 4 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0009 | 0/0 | 3453 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0010 | 0/0 | 3453 | 3 | 0 | 0 | 3 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0011 | 0/0 | 3453 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0012 | 0/0 | 3453 | 3 | 2 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0013 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0014 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0015 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0016 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0017 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0018 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0019 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0020 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0021 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0022 | 0/0 | 3453 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| c0023 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8658 | 43 | 2 | 6 | 25 | 2 | 8 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0002 | 0/1 | 8659 | 24 | 1 | 18 | 0 | 1 | 3 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0003 | 0/0 | 8660 | 19 | 0 | 3 | 14 | 1 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0004 | 0/0 | 8660 | 15 | 2 | 3 | 4 | 2 | 4 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0005 | 0/0 | 8660 | 10 | 0 | 0 | 10 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0006 | 0/0 | 8658 | 5 | 0 | 3 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0007 | 0/0 | 8662 | 4 | 0 | 0 | 4 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0008 | 0/0 | 8657 | 4 | 0 | 2 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0009 | 0/0 | 8683 | 3 | 0 | 1 | 0 | 2 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0010 | 0/0 | 8681 | 3 | 1 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0011 | 0/0 | 8658 | 3 | 0 | 1 | 1 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0012 | 0/0 | 8692 | 3 | 0 | 1 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0013 | 0/0 | 8680 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0014 | 0/0 | 8658 | 3 | 0 | 0 | 3 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0015 | 0/0 | 8660 | 3 | 0 | 0 | 3 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0016 | 0/0 | 8658 | 3 | 0 | 2 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0017 | 0/0 | 8689 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0018 | 0/0 | 8660 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0019 | 0/0 | 8658 | 2 | 0 | 0 | 1 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0020 | 0/0 | 8669 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0021 | 0/0 | 8667 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0022 | 0/0 | 8678 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0023 | 0/0 | 8692 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0024 | 0/0 | 8690 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0025 | 0/0 | 8659 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0026 | 0/0 | 8664 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0027 | 0/0 | 8688 | 2 | 1 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0028 | 0/0 | 8682 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0029 | 0/0 | 8685 | 2 | 1 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0030 | 0/0 | 8687 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0031 | 0/0 | 8690 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0032 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0033 | 0/0 | 8694 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0034 | 0/0 | 8690 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0035 | 0/0 | 8674 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0036 | 0/0 | 8686 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0037 | 0/0 | 8662 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0038 | 0/0 | 8688 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0039 | 0/0 | 8649 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0040 | 0/0 | 8660 | 2 | 0 | 0 | 1 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0041 | 0/0 | 8662 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0042 | 0/0 | 8658 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0043 | 0/0 | 8658 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0044 | 0/0 | 8689 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0045 | 0/0 | 8687 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0046 | 0/0 | 8685 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0047 | 0/0 | 8681 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0048 | 0/0 | 8673 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0049 | 0/0 | 8689 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0050 | 0/0 | 8682 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0051 | 0/0 | 8661 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0052 | 0/0 | 8688 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0053 | 0/0 | 8686 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0054 | 0/0 | 8684 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0055 | 0/0 | 8678 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0056 | 0/0 | 8695 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0057 | 0/0 | 8691 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0058 | 0/0 | 8680 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0059 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0060 | 0/0 | 8685 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0061 | 0/0 | 8693 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0062 | 0/0 | 8687 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0063 | 0/0 | 8693 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0064 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0065 | 0/0 | 8666 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0066 | 0/0 | 8659 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0067 | 0/0 | 8696 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0068 | 0/0 | 8684 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0069 | 0/0 | 8680 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0070 | 0/0 | 8690 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0071 | 0/0 | 8686 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0072 | 0/0 | 8669 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0073 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0074 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0075 | 0/0 | 8660 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0076 | 0/0 | 8668 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0077 | 0/0 | 8658 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0078 | 0/0 | 8686 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0079 | 0/0 | 8716 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0080 | 0/0 | 8686 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0081 | 0/0 | 8658 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0082 | 0/0 | 8657 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0083 | 0/0 | 8692 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0084 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0085 | 0/0 | 8661 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0086 | 0/0 | 8659 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0087 | 0/0 | 8658 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0088 | 0/0 | 8658 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0089 | 0/0 | 8658 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0090 | 0/0 | 8659 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0091 | 0/0 | 8658 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0092 | 0/0 | 8679 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0093 | 0/0 | 8699 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0094 | 0/0 | 8695 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0095 | 0/0 | 8693 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0096 | 1/0 | 8690 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0097 | 0/0 | 8715 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0098 | 0/0 | 8669 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0099 | 0/0 | 8667 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0100 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0101 | 0/0 | 8681 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0102 | 0/0 | 8684 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0103 | 0/0 | 8674 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0104 | 0/0 | 8689 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0105 | 0/0 | 8667 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0106 | 0/0 | 8691 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0107 | 0/0 | 8690 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0108 | 0/0 | 8687 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0109 | 0/0 | 8667 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0110 | 0/0 | 8659 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0111 | 0/0 | 8684 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0112 | 0/0 | 8687 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0113 | 0/0 | 8714 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0114 | 0/0 | 8687 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0115 | 0/0 | 8688 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0116 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0117 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0118 | 0/0 | 8649 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0119 | 0/0 | 8659 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0120 | 0/0 | 8692 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0121 | 0/0 | 8686 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0122 | 0/0 | 8669 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0123 | 0/0 | 8667 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| t0124 | 0/0 | 8661 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3453 | 154 | 29 | 43 | 46 | 6 | 28 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0003 | 0/0 | 3453 | 11 | 0 | 3 | 7 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0007 | 0/0 | 3453 | 5 | 5 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0008 | 0/0 | 3453 | 4 | 4 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0009 | 0/0 | 3453 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0012 | 0/0 | 3453 | 3 | 2 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0020 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002 | 0/0 | 3453 | 65 | 22 | 10 | 26 | 1 | 6 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004 | 0/0 | 3453 | 11 | 10 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0005 | 0/0 | 3453 | 6 | 0 | 3 | 0 | 2 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0006 | 0/0 | 3453 | 5 | 0 | 2 | 0 | 3 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0005c0010 | 0/0 | 3453 | 3 | 0 | 0 | 3 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0006c0011 | 0/0 | 3453 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0007c0013 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0008c0021 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0009c0015 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0010c0014 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0011c0019 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0012c0017 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0013c0016 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0014c0018 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0015c0022 | 0/0 | 3453 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0016c0023 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12110 | 42 | 2 | 6 | 24 | 2 | 8 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0002 | 0/1 | 12111 | 22 | 1 | 17 | 0 | 0 | 3 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0004 | 0/0 | 12112 | 14 | 1 | 3 | 4 | 2 | 4 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0005 | 0/0 | 12112 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0006 | 0/0 | 12110 | 5 | 0 | 3 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0008 | 0/0 | 12109 | 4 | 0 | 2 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0011 | 0/0 | 12110 | 2 | 0 | 1 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0014 | 0/0 | 12110 | 3 | 0 | 0 | 3 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0015 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0016 | 0/0 | 12110 | 3 | 0 | 2 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0017 | 0/0 | 12141 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0019 | 0/0 | 12110 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0023 | 0/0 | 12144 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0025 | 0/0 | 12111 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0030 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0033 | 0/0 | 12146 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0034 | 0/0 | 12142 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0035 | 0/0 | 12126 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0036 | 0/0 | 12138 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0037 | 0/0 | 12114 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0040 | 0/0 | 12112 | 2 | 0 | 0 | 1 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0041 | 0/0 | 12114 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0042 | 0/0 | 12110 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0043 | 0/0 | 12110 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0056 | 0/0 | 12147 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0057 | 0/0 | 12143 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0059 | 0/0 | 12158 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0072 | 0/0 | 12121 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0076 | 0/0 | 12120 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0077 | 0/0 | 12110 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0081 | 0/0 | 12110 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0082 | 0/0 | 12109 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0084 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0085 | 0/0 | 12113 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0086 | 0/0 | 12111 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0087 | 0/0 | 12110 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0088 | 0/0 | 12110 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0089 | 0/0 | 12110 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0090 | 0/0 | 12111 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0091 | 0/0 | 12110 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0092 | 0/0 | 12131 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0093 | 0/0 | 12151 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0094 | 0/0 | 12147 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0095 | 0/0 | 12145 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0096 | 1/0 | 12142 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0106 | 0/0 | 12143 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0107 | 0/0 | 12142 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0109 | 0/0 | 12119 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0110 | 0/0 | 12111 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0111 | 0/0 | 12136 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0112 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0115 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0119 | 0/0 | 12111 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0122 | 0/0 | 12121 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0001t0124 | 0/0 | 12113 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0003t0003 | 0/0 | 12112 | 6 | 0 | 3 | 2 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0003t0005 | 0/0 | 12112 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0003t0018 | 0/0 | 12112 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0003t0019 | 0/0 | 12110 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0007t0039 | 0/0 | 12101 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0007t0116 | 0/0 | 12101 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0007t0117 | 0/0 | 12101 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0007t0118 | 0/0 | 12101 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0008t0038 | 0/0 | 12140 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0008t0083 | 0/0 | 12144 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0008t0103 | 0/0 | 12126 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0009t0049 | 0/0 | 12141 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0009t0097 | 0/0 | 12167 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0009t0113 | 0/0 | 12166 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0012t0002 | 0/0 | 12111 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0012t0078 | 0/0 | 12138 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0012t0080 | 0/0 | 12138 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0001c0020t0058 | 0/0 | 12132 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0003 | 0/0 | 12112 | 13 | 0 | 0 | 12 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0005 | 0/0 | 12112 | 6 | 0 | 0 | 6 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0007 | 0/0 | 12114 | 4 | 0 | 0 | 4 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0010 | 0/0 | 12133 | 3 | 1 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0011 | 0/0 | 12110 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0012 | 0/0 | 12144 | 3 | 0 | 1 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0013 | 0/0 | 12132 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0015 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0017 | 0/0 | 12141 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0020 | 0/0 | 12121 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0021 | 0/0 | 12119 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0026 | 0/0 | 12116 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0027 | 0/0 | 12140 | 2 | 1 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0028 | 0/0 | 12134 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0029 | 0/0 | 12137 | 2 | 1 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0060 | 0/0 | 12137 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0061 | 0/0 | 12145 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0062 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0063 | 0/0 | 12145 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0066 | 0/0 | 12111 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0067 | 0/0 | 12148 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0068 | 0/0 | 12136 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0069 | 0/0 | 12132 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0070 | 0/0 | 12142 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0071 | 0/0 | 12138 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0073 | 0/0 | 12117 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0074 | 0/0 | 12117 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0098 | 0/0 | 12121 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0099 | 0/0 | 12119 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0100 | 0/0 | 12116 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0105 | 0/0 | 12119 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0114 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0120 | 0/0 | 12144 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0002c0002t0121 | 0/0 | 12138 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0024 | 0/0 | 12142 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0031 | 0/0 | 12142 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0032 | 0/0 | 12120 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0052 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0053 | 0/0 | 12138 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0054 | 0/0 | 12136 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0055 | 0/0 | 12130 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0003c0004t0075 | 0/0 | 12112 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0005t0022 | 0/0 | 12130 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0005t0045 | 0/0 | 12139 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0005t0047 | 0/0 | 12133 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0005t0048 | 0/0 | 12125 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0005t0050 | 0/0 | 12134 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0006t0009 | 0/0 | 12135 | 3 | 0 | 1 | 0 | 2 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0006t0046 | 0/0 | 12137 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0004c0006t0101 | 0/0 | 12133 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0005c0010t0026 | 0/0 | 12116 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0005c0010t0064 | 0/0 | 12116 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0005c0010t0065 | 0/0 | 12118 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0006c0011t0036 | 0/0 | 12138 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0006c0011t0104 | 0/0 | 12141 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0006c0011t0108 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0007c0013t0004 | 0/0 | 12112 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0008c0021t0102 | 0/0 | 12136 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0009c0015t0044 | 0/0 | 12141 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0010c0014t0079 | 0/0 | 12168 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0011c0019t0051 | 0/0 | 12113 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0012c0017t0002 | 0/0 | 12111 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0013c0016t0030 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0014c0018t0015 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0015c0022t0123 | 0/0 | 12119 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| a0016c0023t0001 | 0/0 | 12110 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | copy fasta | chr15 | 55606544 | 55748152 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0014g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0014g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0014g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0015g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0016g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0016g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0017g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0019g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0023g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0023g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0025g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0025g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0030g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0033g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0033g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0034g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0034g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0035g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0036g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0037g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0037g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0040g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0040g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0041g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0041g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0042g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0042g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0043g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0043g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0056g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0057g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0059g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0072g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0076g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0077g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0081g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0082g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0084g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0085g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0086g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0087g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0088g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0089g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0090g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0091g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0092g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0093g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0094g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0095g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0096g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0106g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0107g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0109g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0110g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0111g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0112g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0115g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0119g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0122g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0001t0124g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0018g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0018g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0003t0019g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0007t0039g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0007t0039g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0007t0116g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0007t0117g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0007t0118g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0008t0038g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0008t0038g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0008t0083g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0008t0103g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0009t0049g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0009t0097g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0009t0113g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0012t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0012t0078g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0012t0080g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0001c0020t0058g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0010g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0012g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0012g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0012g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0015g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0017g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0020g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0021g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0021g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0026g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0027g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0027g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0028g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0028g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0029g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0029g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0060g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0061g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0062g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0063g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0066g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0067g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0068g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0069g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0070g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0071g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0073g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0074g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0098g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0099g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0100g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0105g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0114g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0120g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0002c0002t0121g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0024g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0024g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0031g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0031g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0032g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0032g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0052g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0053g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0054g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0055g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0003c0004t0075g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0005t0022g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0005t0022g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0005t0045g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0005t0047g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0005t0048g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0005t0050g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0006t0009g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0006t0009g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0006t0009g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0006t0046g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0004c0006t0101g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0005c0010t0026g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0005c0010t0064g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0005c0010t0065g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0006c0011t0036g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0006c0011t0104g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0006c0011t0108g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0007c0013t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0008c0021t0102g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0009c0015t0044g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0010c0014t0079g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0011c0019t0051g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0012c0017t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0013c0016t0030g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0014c0018t0015g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0015c0022t0123g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| a0016c0023t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0005 | t0047 | g0037 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00099 | hp2 | a0004 | c0006 | t0101 | g0146 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00140 | hp1 | a0012 | c0017 | t0002 | g0254 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00280 | hp1 | a0001 | c0003 | t0003 | g0082 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00323 | hp1 | a0002 | c0002 | t0105 | g0212 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00323 | hp2 | a0001 | c0001 | t0011 | g0091 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00408 | hp2 | a0001 | c0003 | t0018 | g0090 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0043 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00642 | hp1 | a0002 | c0002 | t0067 | g0027 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00642 | hp2 | a0002 | c0002 | t0012 | g0018 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0264 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00733 | hp2 | a0004 | c0006 | t0009 | g0015 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00738 | hp1 | a0001 | c0001 | t0037 | g0169 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00738 | hp2 | a0001 | c0001 | t0042 | g0262 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00741 | hp1 | a0004 | c0005 | t0022 | g0039 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01071 | hp1 | a0015 | c0022 | t0123 | g0283 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01071 | hp2 | a0001 | c0001 | t0037 | g0172 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01074 | hp1 | a0002 | c0002 | t0121 | g0237 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01081 | hp1 | a0001 | c0001 | t0011 | g0075 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01081 | hp2 | a0001 | c0012 | t0002 | g0279 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01106 | hp2 | a0004 | c0005 | t0045 | g0040 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01109 | hp1 | a0002 | c0002 | t0061 | g0045 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0180 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01167 | hp2 | a0002 | c0002 | t0010 | g0050 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0152 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01169 | hp1 | a0002 | c0002 | t0010 | g0049 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0153 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01243 | hp1 | a0004 | c0005 | t0022 | g0041 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01243 | hp2 | a0002 | c0002 | t0060 | g0046 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01255 | hp2 | a0003 | c0004 | t0054 | g0055 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01257 | hp1 | a0002 | c0002 | t0066 | g0083 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01257 | hp2 | a0001 | c0001 | t0016 | g0116 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01258 | hp1 | a0001 | c0001 | t0016 | g0175 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0250 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01358 | hp2 | a0004 | c0006 | t0046 | g0012 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01361 | hp1 | a0001 | c0001 | t0025 | g0013 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01361 | hp2 | a0001 | c0001 | t0042 | g0280 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01433 | hp1 | a0002 | c0002 | t0071 | g0014 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01433 | hp2 | a0001 | c0001 | t0025 | g0030 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01515 | hp1 | a0004 | c0006 | t0009 | g0008 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0244 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0255 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01517 | hp2 | a0004 | c0006 | t0009 | g0007 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01884 | hp2 | a0003 | c0004 | t0024 | g0056 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0122 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01891 | hp2 | a0001 | c0001 | t0057 | g0006 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0163 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0073 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0162 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01978 | hp1 | a0001 | c0001 | t0119 | g0160 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0042 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02015 | hp1 | a0001 | c0003 | t0018 | g0081 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02027 | hp1 | a0001 | c0001 | t0041 | g0135 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02027 | hp2 | a0002 | c0002 | t0007 | g0044 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02040 | hp1 | a0001 | c0001 | t0087 | g0148 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02040 | hp2 | a0001 | c0001 | t0089 | g0202 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02055 | hp1 | a0002 | c0002 | t0069 | g0026 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02055 | hp2 | a0001 | c0001 | t0072 | g0094 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02074 | hp1 | a0001 | c0003 | t0019 | g0079 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0069 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02129 | hp2 | a0002 | c0002 | t0015 | g0227 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02145 | hp1 | a0003 | c0004 | t0031 | g0097 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02145 | hp2 | a0001 | c0020 | t0058 | g0002 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02148 | hp2 | a0002 | c0002 | t0099 | g0174 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02257 | hp1 | a0007 | c0013 | t0004 | g0239 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02257 | hp2 | a0001 | c0001 | t0110 | g0217 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02273 | hp2 | a0001 | c0001 | t0081 | g0159 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02300 | hp1 | a0001 | c0001 | t0124 | g0276 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02300 | hp2 | a0001 | c0003 | t0003 | g0080 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02451 | hp1 | a0002 | c0002 | t0029 | g0031 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02451 | hp2 | a0002 | c0002 | t0020 | g0052 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02572 | hp1 | a0001 | c0001 | t0036 | g0218 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02572 | hp2 | a0006 | c0011 | t0108 | g0222 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02615 | hp1 | a0001 | c0009 | t0097 | g0112 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02615 | hp2 | a0002 | c0002 | t0027 | g0023 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02622 | hp1 | a0001 | c0001 | t0112 | g0128 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02622 | hp2 | a0001 | c0001 | t0033 | g0098 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02630 | hp1 | a0001 | c0007 | t0039 | g0230 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02630 | hp2 | a0001 | c0012 | t0080 | g0114 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02647 | hp1 | a0001 | c0001 | t0092 | g0127 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02647 | hp2 | a0001 | c0001 | t0106 | g0229 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02683 | hp1 | a0002 | c0002 | t0012 | g0016 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02698 | hp1 | a0002 | c0002 | t0012 | g0028 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0263 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02717 | hp1 | a0008 | c0021 | t0102 | g0204 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02717 | hp2 | a0002 | c0002 | t0062 | g0025 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02723 | hp1 | a0013 | c0016 | t0030 | g0093 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02723 | hp2 | a0001 | c0007 | t0039 | g0231 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02735 | hp1 | a0002 | c0002 | t0027 | g0029 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02738 | hp1 | a0001 | c0001 | t0088 | g0194 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02809 | hp1 | a0001 | c0001 | t0093 | g0125 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02809 | hp2 | a0011 | c0019 | t0051 | g0003 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02818 | hp1 | a0001 | c0001 | t0059 | g0005 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02818 | hp2 | a0006 | c0011 | t0036 | g0220 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02886 | hp1 | a0002 | c0002 | t0028 | g0021 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02886 | hp2 | a0002 | c0002 | t0098 | g0213 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02922 | hp1 | a0002 | c0002 | t0013 | g0020 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02922 | hp2 | a0002 | c0002 | t0017 | g0126 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02965 | hp1 | a0001 | c0001 | t0034 | g0102 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02965 | hp2 | a0003 | c0004 | t0053 | g0054 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02970 | hp1 | a0002 | c0002 | t0073 | g0104 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02970 | hp2 | a0001 | c0009 | t0113 | g0233 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02976 | hp1 | a0001 | c0001 | t0111 | g0228 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02976 | hp2 | a0006 | c0011 | t0104 | g0219 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03017 | hp1 | a0002 | c0002 | t0029 | g0019 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0247 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03041 | hp1 | a0001 | c0001 | t0095 | g0124 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03041 | hp2 | a0002 | c0002 | t0114 | g0215 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03098 | hp1 | a0001 | c0001 | t0086 | g0197 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03098 | hp2 | a0002 | c0002 | t0021 | g0053 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03130 | hp1 | a0003 | c0004 | t0052 | g0059 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03130 | hp2 | a0002 | c0002 | t0021 | g0010 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03195 | hp1 | a0003 | c0004 | t0032 | g0096 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03195 | hp2 | a0001 | c0001 | t0034 | g0101 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03209 | hp1 | a0002 | c0002 | t0020 | g0060 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03209 | hp2 | a0003 | c0004 | t0024 | g0057 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03225 | hp1 | a0002 | c0002 | t0010 | g0048 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03239 | hp2 | a0009 | c0015 | t0044 | g0011 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03453 | hp1 | a0001 | c0008 | t0038 | g0210 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03453 | hp2 | a0001 | c0012 | t0078 | g0113 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03486 | hp1 | a0001 | c0001 | t0115 | g0205 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03486 | hp2 | a0001 | c0008 | t0038 | g0209 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0282 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03490 | hp2 | a0004 | c0005 | t0050 | g0038 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03491 | hp2 | a0001 | c0001 | t0035 | g0001 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03492 | hp1 | a0001 | c0001 | t0035 | g0001 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0281 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03540 | hp1 | a0001 | c0001 | t0023 | g0051 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03540 | hp2 | a0001 | c0001 | t0030 | g0092 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03579 | hp1 | a0003 | c0004 | t0055 | g0062 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03579 | hp2 | a0001 | c0001 | t0023 | g0058 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03669 | hp1 | a0001 | c0001 | t0085 | g0147 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0009 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03710 | hp1 | a0001 | c0001 | t0043 | g0272 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0201 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03831 | hp1 | a0001 | c0001 | t0019 | g0061 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03831 | hp2 | a0001 | c0001 | t0091 | g0190 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03834 | hp2 | a0001 | c0001 | t0040 | g0132 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03927 | hp2 | a0002 | c0002 | t0070 | g0017 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG04115 | hp1 | a0001 | c0001 | t0043 | g0260 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG04204 | hp2 | a0001 | c0001 | t0122 | g0278 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG04228 | hp1 | a0001 | c0001 | t0107 | g0221 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG04228 | hp2 | a0001 | c0001 | t0077 | g0142 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18522 | hp1 | a0002 | c0002 | t0028 | g0022 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18522 | hp2 | a0003 | c0004 | t0032 | g0095 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18906 | hp1 | a0002 | c0002 | t0074 | g0099 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18906 | hp2 | a0001 | c0009 | t0049 | g0035 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18942 | hp1 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18942 | hp2 | a0001 | c0001 | t0082 | g0145 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18943 | hp1 | a0002 | c0002 | t0005 | g0216 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18943 | hp2 | a0014 | c0018 | t0015 | g0189 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18944 | hp1 | a0005 | c0010 | t0026 | g0065 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18948 | hp2 | a0001 | c0001 | t0008 | g0207 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18951 | hp2 | a0002 | c0002 | t0100 | g0214 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18952 | hp1 | a0001 | c0001 | t0014 | g0154 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18952 | hp2 | a0001 | c0001 | t0040 | g0166 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18953 | hp2 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18954 | hp2 | a0005 | c0010 | t0065 | g0034 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18963 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18964 | hp1 | a0002 | c0002 | t0005 | g0119 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18964 | hp2 | a0001 | c0001 | t0090 | g0139 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18966 | hp1 | a0005 | c0010 | t0064 | g0072 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18966 | hp2 | a0002 | c0002 | t0026 | g0078 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18971 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18971 | hp2 | a0001 | c0001 | t0015 | g0140 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18973 | hp2 | a0001 | c0001 | t0084 | g0192 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18980 | hp1 | a0002 | c0002 | t0003 | g0074 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18981 | hp1 | a0002 | c0002 | t0005 | g0120 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18983 | hp1 | a0001 | c0001 | t0041 | g0136 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA18994 | hp2 | a0001 | c0003 | t0005 | g0225 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19000 | hp1 | a0002 | c0002 | t0007 | g0085 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19002 | hp2 | a0001 | c0001 | t0014 | g0168 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0223 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19007 | hp2 | a0002 | c0002 | t0007 | g0070 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19009 | hp1 | a0016 | c0023 | t0001 | g0235 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0088 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19012 | hp2 | a0002 | c0002 | t0005 | g0108 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19030 | hp1 | a0001 | c0008 | t0083 | g0121 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19030 | hp2 | a0001 | c0007 | t0118 | g0111 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19043 | hp1 | a0001 | c0001 | t0109 | g0232 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19043 | hp2 | a0001 | c0001 | t0056 | g0004 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19054 | hp1 | a0001 | c0003 | t0005 | g0191 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19064 | hp2 | a0002 | c0002 | t0005 | g0118 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19066 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19077 | hp2 | a0002 | c0002 | t0005 | g0117 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19078 | hp1 | a0002 | c0002 | t0011 | g0084 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19078 | hp2 | a0001 | c0001 | t0014 | g0167 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19080 | hp1 | a0002 | c0002 | t0007 | g0064 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0086 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19240 | hp1 | a0001 | c0001 | t0033 | g0103 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA19240 | hp2 | a0001 | c0007 | t0117 | g0110 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA20129 | hp1 | a0010 | c0014 | t0079 | g0234 | AFR | ASW | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA20129 | hp2 | a0001 | c0008 | t0103 | g0208 | AFR | ASW | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA20805 | hp1 | a0004 | c0005 | t0048 | g0036 | EUR | TSI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA20805 | hp2 | a0001 | c0001 | t0076 | g0133 | EUR | TSI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02109 | hp1 | a0001 | c0001 | t0017 | g0123 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02109 | hp2 | a0001 | c0007 | t0116 | g0109 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02486 | hp1 | a0002 | c0002 | t0013 | g0024 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02559 | hp1 | a0002 | c0002 | t0063 | g0047 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG02559 | hp2 | a0002 | c0002 | t0013 | g0033 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03471 | hp1 | a0001 | c0001 | t0094 | g0129 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| HG03471 | hp2 | a0003 | c0004 | t0031 | g0105 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA20300 | hp1 | a0002 | c0002 | t0120 | g0236 | AFR | USA | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA20300 | hp2 | a0002 | c0002 | t0068 | g0032 | AFR | USA | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA21309 | hp1 | a0003 | c0004 | t0075 | g0100 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0245 | REF | REF | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0096 | g0211 | REF | REF | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:55620036
|
T | C | 1 | a0008 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.3429A>G | p.Ile1143Met | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3650/12142 | 3429/3453 | 1143/1150 | chr15 | 55620036 | ||
| chr15:55620062
|
C | T | 1 | a0013 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.3403G>A | p.Asp1135Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3624/12142 | 3403/3453 | 1135/1150 | chr15 | 55620062 | ||
| chr15:55620193
|
G | A | 1 | a0012 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.3272C>T | p.Ser1091Phe | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3493/12142 | 3272/3453 | 1091/1150 | chr15 | 55620193 | ||
| chr15:55620677
|
T | A | 2 | a0004a0009 | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
missense_variant | MODERATE | c.3184A>T | p.Ile1062Leu | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/20 | 3405/12142 | 3184/3453 | 1062/1150 | chr15 | 55620677 | ||
| chr15:55624362
|
T | A | 1 | a0014 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.3073A>T | p.Asn1025Tyr | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/20 | 3294/12142 | 3073/3453 | 1025/1150 | chr15 | 55624362 | ||
| chr15:55624458
|
G | A | 1 | a0011 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.2977C>T | p.Arg993Cys | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/20 | 3198/12142 | 2977/3453 | 993/1150 | chr15 | 55624458 | ||
| chr15:55624487
|
G | A | 1 | a0010 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2948C>T | p.Thr983Met | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/20 | 3169/12142 | 2948/3453 | 983/1150 | chr15 | 55624487 | ||
| chr15:55628845
|
C | T | 1 | a0005 | 3 | NA18944.hp1 NA18954.hp2 NA18966.hp1 |
missense_variant | MODERATE | c.2783G>A | p.Arg928His | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/20 | 3004/12142 | 2783/3453 | 928/1150 | chr15 | 55628845 | ||
| chr15:55637317
|
C | G | 1 | a0003 | 11 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
missense_variant | MODERATE | c.2476G>C | p.Val826Leu | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/20 | 2697/12142 | 2476/3453 | 826/1150 | chr15 | 55637317 | ||
| chr15:55672580
|
C | G | 1 | a0009 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1906G>C | p.Val636Leu | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/20 | 2127/12142 | 1906/3453 | 636/1150 | chr15 | 55672580 | ||
| chr15:55680599
|
T | C | 3 | a0002a0005a0008 | 69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
missense_variant | MODERATE | c.706A>G | p.Thr236Ala | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/20 | 927/12142 | 706/3453 | 236/1150 | chr15 | 55680599 | ||
| chr15:55683859
|
T | C | 1 | a0006 | 3 | HG02572.hp2 HG02818.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.470A>G | p.Lys157Arg | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/20 | 691/12142 | 470/3453 | 157/1150 | chr15 | 55683859 | ||
| chr15:55740467
|
C | G | 1 | a0007 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.312G>C | p.Glu104Asp | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/20 | 533/12142 | 312/3453 | 104/1150 | chr15 | 55740467 | ||
| chr15:55742895
|
G | A | 1 | a0015 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.37C>T | p.Pro13Ser | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 258/12142 | 37/3453 | 13/1150 | chr15 | 55742895 | ||
| chr15:55742924
|
G | C | 1 | a0016 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.8C>G | p.Pro3Arg | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 229/12142 | 8/3453 | 3/1150 | chr15 | 55742924 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:55638637
|
G | A | 3 | a0001c0007a0001c0008a0003c0004 | 20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
synonymous_variant | LOW | c.2364C>T | p.Asn788Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/20 | 2585/12142 | 2364/3453 | 788/1150 | chr15 | 55638637 | ||
| chr15:55641159
|
G | A | 1 | a0001c0020 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.2091C>T | p.Asp697Asp | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/20 | 2312/12142 | 2091/3453 | 697/1150 | chr15 | 55641159 | ||
| chr15:55673504
|
C | T | 3 | a0001c0008a0001c0009a0010c0014 | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
synonymous_variant | LOW | c.1719G>A | p.Thr573Thr | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/20 | 1940/12142 | 1719/3453 | 573/1150 | chr15 | 55673504 | ||
| chr15:55677843
|
A | G | 4 | a0001c0003a0002c0002a0005c0010others(1): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
synonymous_variant | LOW | c.1335T>C | p.Asn445Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/20 | 1556/12142 | 1335/3453 | 445/1150 | chr15 | 55677843 | ||
| chr15:55740509
|
G | A | 1 | a0001c0012 | 3 | HG01081.hp2 HG02630.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.270C>T | p.Asn90Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/20 | 491/12142 | 270/3453 | 90/1150 | chr15 | 55740509 | ||
| chr15:55740674
|
G | A | 1 | a0004c0005 | 6 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(3): Show |
synonymous_variant | LOW | c.105C>T | p.Cys35Cys | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/20 | 326/12142 | 105/3453 | 35/1150 | chr15 | 55740674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:55611551
|
T | C | 1 | a0001c0001t0087 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8461A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8461 | chr15 | 55611551 | |||||
| chr15:55611722
|
A | G | 1 | a0001c0001t0110 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8290T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8290 | chr15 | 55611722 | |||||
| chr15:55611731
|
A | T | 1 | a0001c0001t0076 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8281T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8281 | chr15 | 55611731 | |||||
| chr15:55611751
|
A | G | 1 | a0002c0002t0068 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8261T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8261 | chr15 | 55611751 | |||||
| chr15:55611892
|
G | C | 40 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(37): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*8120C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8120 | chr15 | 55611892 | |||||
| chr15:55611929
|
T | C | 1 | a0001c0001t0106 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8083A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8083 | chr15 | 55611929 | |||||
| chr15:55612019
|
GA | G | 83 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(80): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*7992delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7992 | chr15 | 55612019 | |||||
| chr15:55612046
|
T | C | 116 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(113): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*7966A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7966 | chr15 | 55612046 | |||||
| chr15:55612529
|
G | A | 23 | a0001c0001t0002a0001c0001t0004a0001c0001t0025others(20): Show | 62 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*7483C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7483 | chr15 | 55612529 | |||||
| chr15:55612575
|
T | C | 1 | a0011c0019t0051 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7437A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7437 | chr15 | 55612575 | |||||
| chr15:55612633
|
C | T | 1 | a0003c0004t0032 | 2 | HG03195.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7379G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7379 | chr15 | 55612633 | |||||
| chr15:55612696
|
C | CCATATAT others(21): Show |
1 | a0010c0014t0079 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7315_*7316insCATA others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7315 | chr15 | 55612696 | |||||
| chr15:55612696
|
CAATATAT others(3): Show |
C | 1 | a0001c0001t0092 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7306_*7315delTATA others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7306 | chr15 | 55612696 | |||||
| chr15:55612697
|
A | AAT | 7 | a0001c0001t0034a0001c0001t0057a0001c0001t0106others(4): Show | 12 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7313_*7314dupAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | |||||
| chr15:55612697
|
A | AATAT | 5 | a0001c0001t0023a0001c0001t0095a0001c0008t0083others(2): Show | 6 | HG01109.hp1 HG02559.hp1 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7311_*7314dupATAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | |||||
| chr15:55612697
|
A | AATATAT | 4 | a0001c0001t0033a0001c0001t0056a0001c0001t0094others(1): Show | 5 | HG00642.hp1 HG02622.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7309_*7314dupATAT others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | |||||
| chr15:55612697
|
A | AATATATA others(3): Show |
1 | a0001c0001t0093 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7305_*7314dupATAT others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | |||||
| chr15:55612697
|
A | C | 4 | a0001c0001t0059a0001c0009t0049a0001c0009t0097others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7315T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7315 | chr15 | 55612697 | |||||
| chr15:55612697
|
A | T | 5 | a0001c0001t0036a0001c0001t0112a0001c0012t0080others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7315T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7315 | chr15 | 55612697 | |||||
| chr15:55612697
|
AAT | A | 9 | a0001c0001t0030a0001c0001t0115a0002c0002t0027others(6): Show | 10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7313_*7314delAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7313 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATAT | A | 8 | a0001c0001t0111a0002c0002t0029a0002c0002t0060others(5): Show | 9 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7311_*7314delATAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7311 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATAT | A | 3 | a0002c0002t0068a0004c0005t0050a0004c0006t0046 | 3 | HG01358.hp2 HG03490.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7309_*7314delATAT others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7309 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(1): Show |
A | 3 | a0002c0002t0010a0002c0002t0028a0004c0006t0009 | 8 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7307_*7314delATAT others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7307 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(3): Show |
A | 7 | a0001c0020t0058a0002c0002t0013a0002c0002t0069others(4): Show | 10 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7305_*7314delATAT others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7305 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(7): Show |
A | 2 | a0001c0001t0035a0001c0008t0103 | 3 | HG03491.hp2 HG03492.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7301_*7314delATAT others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7301 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(11): Show |
A | 1 | a0004c0005t0048 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7297_*7314delATAT others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7297 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(13): Show |
A | 7 | a0001c0001t0072a0001c0001t0076a0001c0001t0122others(4): Show | 9 | HG02055.hp2 HG02451.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7295_*7314delATAT others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7295 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(15): Show |
A | 8 | a0001c0001t0109a0002c0002t0021a0002c0002t0026others(5): Show | 9 | HG00323.hp1 HG01071.hp1 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7293_*7314delATAT others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7293 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(17): Show |
A | 6 | a0001c0001t0037a0001c0001t0041a0002c0002t0007others(3): Show | 11 | HG00738.hp1 HG01071.hp2 HG02027.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7291_*7314delATAT others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7291 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(19): Show |
A | 13 | a0001c0001t0005a0001c0001t0015a0001c0001t0084others(10): Show | 38 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*7289_*7314delATAT others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7289 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(21): Show |
A | 23 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(20): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*7287_*7314delATAT others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7287 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(23): Show |
A | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0025others(6): Show | 46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*7285_*7314delATAT others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7285 | chr15 | 55612697 | |||||
| chr15:55612697
|
AATATATA others(31): Show |
A | 4 | a0001c0007t0039a0001c0007t0116a0001c0007t0117others(1): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7277_*7314delATAT others(34): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7277 | chr15 | 55612697 | |||||
| chr15:55612737
|
T | C | 1 | a0010c0014t0079 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7275A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7275 | chr15 | 55612737 | |||||
| chr15:55612737
|
T | TATATATA others(9): Show |
1 | a0001c0001t0059 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7274_*7275insGTAT others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7274 | chr15 | 55612737 | |||||
| chr15:55612737
|
T | TATATATA others(17): Show |
1 | a0001c0009t0113 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7274_*7275insGTAT others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7274 | chr15 | 55612737 | |||||
| chr15:55612737
|
T | TATATATA others(19): Show |
1 | a0001c0009t0097 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7274_*7275insGTAT others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7274 | chr15 | 55612737 | |||||
| chr15:55612747
|
T | C | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0025others(7): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*7265A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7265 | chr15 | 55612747 | |||||
| chr15:55612903
|
C | A | 1 | a0001c0001t0088 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7109G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7109 | chr15 | 55612903 | |||||
| chr15:55612948
|
T | C | 1 | a0001c0012t0080 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7064A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7064 | chr15 | 55612948 | |||||
| chr15:55613098
|
A | C | 5 | a0001c0001t0036a0001c0001t0112a0001c0012t0078others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6914T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6914 | chr15 | 55613098 | |||||
| chr15:55613233
|
T | C | 1 | a0002c0002t0069 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6779A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6779 | chr15 | 55613233 | |||||
| chr15:55613491
|
G | A | 1 | a0001c0001t0089 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6521C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6521 | chr15 | 55613491 | |||||
| chr15:55613759
|
C | CT | 22 | a0001c0001t0004a0001c0001t0040a0001c0001t0059others(19): Show | 42 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*6252dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6252 | chr15 | 55613759 | |||||
| chr15:55613759
|
C | CTTT | 7 | a0004c0005t0045a0004c0005t0047a0004c0005t0048others(4): Show | 9 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6250_*6252dupAAA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6252 | chr15 | 55613759 | |||||
| chr15:55613759
|
CT | C | 14 | a0001c0001t0023a0001c0001t0033a0001c0001t0034others(11): Show | 19 | HG01978.hp1 HG02109.hp2 HG02622.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6252delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6252 | chr15 | 55613759 | |||||
| chr15:55613759
|
CTT | C | 38 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(35): Show | 119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*6251_*6252delAA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6251 | chr15 | 55613759 | |||||
| chr15:55613759
|
CTTT | C | 4 | a0001c0001t0008a0001c0001t0082a0001c0001t0090others(1): Show | 7 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6250_*6252delAAA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6250 | chr15 | 55613759 | |||||
| chr15:55613812
|
A | G | 28 | a0001c0001t0030a0001c0001t0072a0001c0001t0122others(25): Show | 39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6200T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6200 | chr15 | 55613812 | |||||
| chr15:55614284
|
T | C | 23 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(20): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*5728A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5728 | chr15 | 55614284 | |||||
| chr15:55614359
|
A | C | 2 | a0002c0002t0010a0002c0002t0060 | 4 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5653T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5653 | chr15 | 55614359 | |||||
| chr15:55614444
|
A | C | 1 | a0002c0002t0074 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5568T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5568 | chr15 | 55614444 | |||||
| chr15:55614616
|
C | T | 4 | a0001c0001t0036a0001c0012t0078a0001c0012t0080others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5396G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5396 | chr15 | 55614616 | |||||
| chr15:55614690
|
T | C | 1 | a0001c0001t0091 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5322A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5322 | chr15 | 55614690 | |||||
| chr15:55614898
|
C | T | 1 | a0001c0007t0116 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5114G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5114 | chr15 | 55614898 | |||||
| chr15:55614919
|
C | T | 2 | a0001c0001t0035a0001c0001t0076 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5093G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5093 | chr15 | 55614919 | |||||
| chr15:55614983
|
G | A | 2 | a0001c0001t0035a0001c0001t0076 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5029C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5029 | chr15 | 55614983 | |||||
| chr15:55615225
|
G | A | 1 | a0002c0002t0070 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4787C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4787 | chr15 | 55615225 | |||||
| chr15:55615239
|
C | G | 1 | a0001c0001t0092 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4773G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4773 | chr15 | 55615239 | |||||
| chr15:55615713
|
A | G | 1 | a0006c0011t0104 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4299T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4299 | chr15 | 55615713 | |||||
| chr15:55615776
|
T | C | 15 | a0001c0007t0039a0001c0007t0116a0001c0007t0117others(12): Show | 20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4236A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4236 | chr15 | 55615776 | |||||
| chr15:55616005
|
T | C | 24 | a0001c0001t0002a0001c0001t0004a0001c0001t0025others(21): Show | 63 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4007A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4007 | chr15 | 55616005 | |||||
| chr15:55616410
|
A | C | 2 | a0001c0009t0113a0010c0014t0079 | 2 | HG02970.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3602T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3602 | chr15 | 55616410 | |||||
| chr15:55616419
|
A | T | 1 | a0010c0014t0079 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3593T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3593 | chr15 | 55616419 | |||||
| chr15:55616511
|
A | C | 1 | a0002c0002t0073 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3501T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3501 | chr15 | 55616511 | |||||
| chr15:55616685
|
T | C | 3 | a0001c0001t0030a0002c0002t0120a0013c0016t0030 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3327A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3327 | chr15 | 55616685 | |||||
| chr15:55616907
|
T | C | 2 | a0001c0001t0035a0001c0001t0076 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3105A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3105 | chr15 | 55616907 | |||||
| chr15:55616967
|
T | C | 1 | a0010c0014t0079 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3045A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3045 | chr15 | 55616967 | |||||
| chr15:55617223
|
TA | T | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(126): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*2788delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2788 | chr15 | 55617223 | |||||
| chr15:55617391
|
A | G | 4 | a0001c0001t0036a0001c0012t0078a0001c0012t0080others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2621T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2621 | chr15 | 55617391 | |||||
| chr15:55617419
|
T | C | 18 | a0001c0001t0030a0002c0002t0010a0002c0002t0012others(15): Show | 27 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2593A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2593 | chr15 | 55617419 | |||||
| chr15:55617752
|
T | C | 2 | a0001c0009t0113a0010c0014t0079 | 2 | HG02970.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2260A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2260 | chr15 | 55617752 | |||||
| chr15:55617758
|
T | C | 1 | a0002c0002t0114 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2254A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2254 | chr15 | 55617758 | |||||
| chr15:55617807
|
A | G | 1 | a0001c0009t0097 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2205T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2205 | chr15 | 55617807 | |||||
| chr15:55617940
|
T | C | 132 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(129): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*2072A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2072 | chr15 | 55617940 | |||||
| chr15:55618059
|
G | A | 1 | a0001c0001t0115 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1953 | chr15 | 55618059 | |||||
| chr15:55618177
|
T | C | 1 | a0002c0002t0071 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1835A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1835 | chr15 | 55618177 | |||||
| chr15:55618199
|
T | C | 8 | a0001c0001t0030a0002c0002t0010a0002c0002t0060others(5): Show | 10 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1813A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1813 | chr15 | 55618199 | |||||
| chr15:55618240
|
A | T | 40 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(37): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1772T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1772 | chr15 | 55618240 | |||||
| chr15:55618465
|
C | T | 1 | a0001c0008t0083 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1547 | chr15 | 55618465 | |||||
| chr15:55618482
|
C | G | 1 | a0005c0010t0064 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1530 | chr15 | 55618482 | |||||
| chr15:55618562
|
C | T | 2 | a0001c0007t0116a0001c0007t0117 | 2 | HG02109.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1450G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1450 | chr15 | 55618562 | |||||
| chr15:55618572
|
A | G | 2 | a0001c0001t0014a0001c0001t0082 | 4 | NA18942.hp2 NA18952.hp1 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1440T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1440 | chr15 | 55618572 | |||||
| chr15:55618755
|
A | G | 1 | a0001c0001t0081 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1257T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1257 | chr15 | 55618755 | |||||
| chr15:55618761
|
C | T | 4 | a0001c0001t0036a0001c0012t0078a0001c0012t0080others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1251G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1251 | chr15 | 55618761 | |||||
| chr15:55619008
|
C | A | 3 | a0001c0007t0116a0001c0007t0117a0001c0007t0118 | 3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1004G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1004 | chr15 | 55619008 | |||||
| chr15:55619342
|
C | T | 2 | a0001c0001t0035a0001c0001t0076 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 670 | chr15 | 55619342 | |||||
| chr15:55619367
|
C | T | 1 | a0010c0014t0079 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 645 | chr15 | 55619367 | |||||
| chr15:55619470
|
C | A | 15 | a0001c0001t0005a0001c0001t0011a0001c0001t0041others(12): Show | 44 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*542G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 542 | chr15 | 55619470 | |||||
| chr15:55619497
|
A | C | 1 | a0001c0012t0078 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*515T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 515 | chr15 | 55619497 | |||||
| chr15:55619500
|
C | T | 1 | a0001c0001t0077 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 512 | chr15 | 55619500 | |||||
| chr15:55619615
|
G | C | 10 | a0002c0002t0012a0002c0002t0013a0002c0002t0027others(7): Show | 17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 397 | chr15 | 55619615 | |||||
| chr15:55619656
|
T | C | 1 | a0002c0002t0071 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*356A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 356 | chr15 | 55619656 | |||||
| chr15:55619674
|
C | T | 2 | a0001c0001t0035a0001c0001t0076 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*338G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 338 | chr15 | 55619674 | |||||
| chr15:55619859
|
G | A | 2 | a0001c0001t0006a0001c0001t0119 | 6 | HG01109.hp2 HG01928.hp2 HG01952.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*153C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 153 | chr15 | 55619859 | |||||
| chr15:55743041
|
C | G | 7 | a0001c0001t0033a0001c0001t0034a0002c0002t0073others(4): Show | 11 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-110G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 110 | chr15 | 55743041 | |||||
| chr15:55743043
|
C | T | 3 | a0001c0001t0030a0001c0001t0072a0013c0016t0030 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
5_prime_UTR_variant | MODIFIER | c.-112G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 112 | chr15 | 55743043 | |||||
| chr15:55743050
|
G | A | 1 | a0002c0002t0120 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-119C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 119 | chr15 | 55743050 | |||||
| chr15:55743059
|
C | G | 52 | a0001c0001t0011a0001c0001t0019a0001c0001t0023others(49): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | chr15 | 55743059 | ||||||
| chr15:55743123
|
G | A | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0042others(8): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-192C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 192 | chr15 | 55743123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:55620330
|
C | T | 7 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(4): Show | 7 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.3199-64G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620330 | ||||||
| chr15:55620373
|
G | A | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3199-107C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620373 | ||||||
| chr15:55620475
|
T | C | 2 | a0003c0004t0031g0105a0003c0004t0075g0100 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3198+188A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620475 | ||||||
| chr15:55620580
|
C | G | 5 | a0001c0001t0036g0218a0001c0001t0112g0128a0001c0012t0078g0113others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3198+83G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620580 | ||||||
| chr15:55620655
|
T | G | 1 | a0001c0003t0003g0073 | 1 | HG01943.hp1 | splice_region_variant&intron_variant | LOW | c.3198+8A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620655 | ||||||
| chr15:55621138
|
G | A | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-371C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621138 | ||||||
| chr15:55621274
|
C | G | 1 | a0001c0001t0011g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3094-507G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621274 | ||||||
| chr15:55621344
|
C | T | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-577G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621344 | ||||||
| chr15:55621357
|
A | T | 1 | a0001c0001t0041g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3094-590T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621357 | ||||||
| chr15:55621386
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0086g0197 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3094-619C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621386 | ||||||
| chr15:55621428
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3094-661G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621428 | ||||||
| chr15:55621432
|
C | T | 2 | a0001c0001t0004g0281a0001c0001t0004g0282 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3094-665G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621432 | ||||||
| chr15:55621527
|
C | T | 80 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.3094-760G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621527 | ||||||
| chr15:55621583
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3094-816G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621583 | ||||||
| chr15:55621584
|
G | A | 5 | a0001c0001t0036g0218a0001c0001t0112g0128a0001c0012t0078g0113others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-817C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621584 | ||||||
| chr15:55621605
|
C | T | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-838G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621605 | ||||||
| chr15:55621886
|
T | C | 28 | a0001c0001t0036g0218a0001c0001t0056g0004a0001c0001t0057g0006others(25): Show | 28 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3094-1119A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621886 | ||||||
| chr15:55622150
|
T | C | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-1383A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622150 | ||||||
| chr15:55622216
|
G | GT | 85 | a0001c0001t0001g0206a0001c0001t0002g0246a0001c0001t0002g0261others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.3094-1450dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622216 | ||||||
| chr15:55622216
|
G | GTT | 85 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3094-1451_3094-145 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622216 | ||||||
| chr15:55622216
|
GT | G | 9 | a0001c0001t0092g0127a0001c0001t0093g0125a0001c0001t0095g0124others(6): Show | 9 | HG02145.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-1450delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622216 | ||||||
| chr15:55622384
|
AT | A | 14 | a0001c0001t0001g0171a0001c0001t0001g0188a0001c0001t0002g0271others(11): Show | 14 | HG01891.hp2 HG01981.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.3094-1618delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622384 | ||||||
| chr15:55622384
|
ATT | A | 258 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3094-1619_3094-161 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622384 | ||||||
| chr15:55622415
|
G | A | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3094-1648C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622415 | ||||||
| chr15:55622564
|
TA | T | 269 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.3093+1777delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622564 | ||||||
| chr15:55622565
|
A | T | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3093+1777T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622565 | ||||||
| chr15:55622604
|
G | A | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3093+1738C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622604 | ||||||
| chr15:55622623
|
C | T | 1 | a0001c0001t0042g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3093+1719G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622623 | ||||||
| chr15:55622694
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3093+1648G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622694 | ||||||
| chr15:55622818
|
G | C | 9 | a0001c0001t0036g0218a0001c0001t0059g0005a0001c0009t0049g0035others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3093+1524C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622818 | ||||||
| chr15:55622870
|
T | C | 1 | a0001c0001t0084g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3093+1472A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622870 | ||||||
| chr15:55623062
|
C | A | 4 | a0001c0001t0036g0218a0001c0012t0078g0113a0001c0012t0080g0114others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+1280G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623062 | ||||||
| chr15:55623084
|
G | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0182a0001c0001t0014g0154others(5): Show | 8 | NA18942.hp2 NA18952.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.3093+1258C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623084 | ||||||
| chr15:55623435
|
C | T | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3093+907G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623435 | ||||||
| chr15:55623452
|
G | A | 60 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(57): Show | 60 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.3093+890C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623452 | ||||||
| chr15:55623497
|
T | C | 233 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.3093+845A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623497 | ||||||
| chr15:55623520
|
C | T | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3093+822G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623520 | ||||||
| chr15:55623563
|
T | A | 6 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0041g0135others(3): Show | 6 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.3093+779A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623563 | ||||||
| chr15:55623702
|
G | A | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3093+640C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623702 | ||||||
| chr15:55623835
|
T | C | 40 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0072g0094others(37): Show | 40 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3093+507A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623835 | ||||||
| chr15:55624158
|
T | C | 1 | a0001c0001t0077g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3093+184A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624158 | ||||||
| chr15:55624175
|
CCCT | C | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3093+164_3093+166d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624175 | ||||||
| chr15:55624240
|
G | C | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+102C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624240 | ||||||
| chr15:55624241
|
T | C | 1 | a0001c0020t0058g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3093+101A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624241 | ||||||
| chr15:55624261
|
A | G | 4 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(1): Show | 4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3093+81T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624261 | ||||||
| chr15:55624636
|
G | A | 1 | a0001c0001t0087g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2928-129C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55624636 | ||||||
| chr15:55624868
|
G | T | 127 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2928-361C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55624868 | ||||||
| chr15:55625353
|
G | A | 1 | a0002c0002t0061g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2928-846C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625353 | ||||||
| chr15:55625432
|
G | A | 1 | a0010c0014t0079g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2928-925C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625432 | ||||||
| chr15:55625469
|
A | T | 1 | a0001c0003t0003g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2928-962T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625469 | ||||||
| chr15:55625515
|
G | A | 1 | a0001c0001t0006g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2928-1008C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625515 | ||||||
| chr15:55625563
|
C | T | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2928-1056G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625563 | ||||||
| chr15:55625609
|
T | A | 1 | a0001c0001t0110g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2928-1102A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625609 | ||||||
| chr15:55625626
|
C | CT | 41 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0072g0094others(38): Show | 41 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2928-1120dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625626 | ||||||
| chr15:55625681
|
T | C | 1 | a0002c0002t0003g0009 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2928-1174A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625681 | ||||||
| chr15:55625707
|
T | TC | 62 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(59): Show | 62 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.2928-1201dupG | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625707 | ||||||
| chr15:55625768
|
C | T | 49 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.2927+1240G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625768 | ||||||
| chr15:55625819
|
C | T | 19 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0257others(16): Show | 19 | HG00733.hp1 HG01168.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.2927+1189G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625819 | ||||||
| chr15:55625853
|
C | T | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2927+1155G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625853 | ||||||
| chr15:55625874
|
C | T | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2927+1134G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625874 | ||||||
| chr15:55625948
|
T | G | 8 | a0001c0001t0001g0144a0001c0001t0001g0198a0001c0001t0014g0154others(5): Show | 8 | HG00408.hp1 NA18942.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2927+1060A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625948 | ||||||
| chr15:55625954
|
T | C | 1 | a0001c0012t0078g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2927+1054A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625954 | ||||||
| chr15:55625979
|
C | T | 1 | a0013c0016t0030g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2927+1029G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625979 | ||||||
| chr15:55626298
|
A | G | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2927+710T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626298 | ||||||
| chr15:55626314
|
C | G | 1 | a0001c0001t0001g0155 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2927+694G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626314 | ||||||
| chr15:55626386
|
G | A | 23 | a0002c0002t0010g0048a0002c0002t0010g0049a0002c0002t0010g0050others(20): Show | 23 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2927+622C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626386 | ||||||
| chr15:55626460
|
T | C | 4 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(1): Show | 4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2927+548A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626460 | ||||||
| chr15:55626500
|
T | C | 2 | a0001c0001t0072g0094a0002c0002t0020g0060 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2927+508A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626500 | ||||||
| chr15:55626515
|
G | C | 48 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(45): Show | 48 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2927+493C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626515 | ||||||
| chr15:55626576
|
C | G | 1 | a0002c0002t0003g0009 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2927+432G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626576 | ||||||
| chr15:55626586
|
T | TA | 5 | a0001c0001t0036g0218a0001c0001t0112g0128a0001c0012t0078g0113others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927+421dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626586 | ||||||
| chr15:55626594
|
C | CA | 7 | a0001c0001t0001g0156a0001c0001t0001g0184a0001c0001t0001g0200others(4): Show | 7 | HG01934.hp2 HG02615.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2927+413dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626594 | ||||||
| chr15:55626594
|
CA | C | 37 | a0001c0001t0041g0135a0001c0001t0072g0094a0001c0001t0122g0278others(34): Show | 37 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2927+413delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626594 | ||||||
| chr15:55626706
|
C | T | 5 | a0001c0001t0036g0218a0001c0001t0112g0128a0001c0012t0078g0113others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927+302G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626706 | ||||||
| chr15:55626716
|
C | G | 62 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(59): Show | 62 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.2927+292G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626716 | ||||||
| chr15:55626765
|
TAAAAG | T | 4 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(1): Show | 4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2927+238_2927+242d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626765 | ||||||
| chr15:55626941
|
T | G | 77 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2927+67A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626941 | ||||||
| chr15:55627326
|
G | GT | 47 | a0001c0001t0001g0144a0001c0001t0002g0269a0001c0001t0005g0141others(44): Show | 47 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.2807-199dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | ||||||
| chr15:55627326
|
G | GTT | 76 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2807-200_2807-199d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | ||||||
| chr15:55627326
|
G | GTTT | 6 | a0001c0001t0001g0130a0001c0001t0001g0156a0001c0001t0001g0200others(3): Show | 6 | HG00438.hp1 HG01361.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2807-201_2807-199d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | ||||||
| chr15:55627326
|
GT | G | 30 | a0001c0001t0036g0218a0001c0001t0059g0005a0001c0007t0039g0230others(27): Show | 30 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2807-199delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | ||||||
| chr15:55627385
|
G | A | 139 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.2807-257C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627385 | ||||||
| chr15:55627492
|
GT | G | 197 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.2807-365delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627492 | ||||||
| chr15:55627515
|
T | G | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2807-387A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627515 | ||||||
| chr15:55627582
|
C | T | 44 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0072g0094others(41): Show | 44 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.2807-454G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627582 | ||||||
| chr15:55627592
|
G | A | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.2807-464C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627592 | ||||||
| chr15:55627715
|
C | T | 1 | a0002c0002t0012g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2807-587G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627715 | ||||||
| chr15:55627830
|
C | T | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2807-702G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627830 | ||||||
| chr15:55627851
|
T | C | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.2807-723A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627851 | ||||||
| chr15:55627881
|
C | T | 2 | a0001c0009t0113g0233a0010c0014t0079g0234 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2807-753G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627881 | ||||||
| chr15:55627911
|
C | A | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2807-783G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627911 | ||||||
| chr15:55627931
|
C | T | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2807-803G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627931 | ||||||
| chr15:55628024
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2806+798G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628024 | ||||||
| chr15:55628142
|
T | G | 5 | a0002c0002t0010g0048a0002c0002t0010g0049a0002c0002t0010g0050others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.2806+680A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628142 | ||||||
| chr15:55628285
|
G | A | 4 | a0001c0001t0041g0135a0001c0001t0041g0136a0001c0001t0077g0142others(1): Show | 4 | HG02027.hp1 HG04228.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2806+537C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628285 | ||||||
| chr15:55628358
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2806+464A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628358 | ||||||
| chr15:55628386
|
GA | G | 240 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(237): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2806+435delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628386 | ||||||
| chr15:55628386
|
GAA | G | 19 | a0001c0001t0001g0188a0001c0001t0002g0265a0001c0001t0005g0164others(16): Show | 20 | HG00099.hp1 HG00438.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2806+434_2806+435d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628386 | ||||||
| chr15:55628387
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2806+435T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628387 | ||||||
| chr15:55628389
|
A | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2806+433T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628389 | ||||||
| chr15:55628514
|
C | A | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2806+308G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628514 | ||||||
| chr15:55628815
|
T | C | 125 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
splice_region_variant&intron_variant | LOW | c.2806+7A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628815 | ||||||
| chr15:55629028
|
T | G | 1 | a0001c0001t0106g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-24A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629028 | ||||||
| chr15:55629278
|
T | C | 1 | a0002c0002t0011g0084 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2624-274A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629278 | ||||||
| chr15:55629303
|
T | C | 20 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2624-299A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629303 | ||||||
| chr15:55629351
|
T | C | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2624-347A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629351 | ||||||
| chr15:55629359
|
GTA | G | 8 | a0001c0001t0002g0257a0001c0001t0004g0247a0001c0001t0004g0255others(5): Show | 8 | HG00140.hp1 HG01517.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2624-357_2624-356d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629359 | ||||||
| chr15:55629359
|
GTATA | G | 3 | a0003c0004t0024g0056a0003c0004t0031g0105a0003c0004t0075g0100 | 3 | HG01884.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2624-359_2624-356d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629359 | ||||||
| chr15:55629363
|
ATATATAT others(31): Show |
A | 1 | a0002c0002t0074g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-397_2624-360d others(40): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629363 | ||||||
| chr15:55629367
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0179a0001c0001t0014g0167a0001c0003t0019g0079 | 3 | HG01993.hp2 HG02074.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2624-373_2624-364d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(5): Show |
A | 13 | a0001c0001t0001g0134a0001c0001t0001g0151a0001c0001t0001g0158others(10): Show | 13 | HG01074.hp2 HG01975.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2624-375_2624-364d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(7): Show |
A | 85 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2624-377_2624-364d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(9): Show |
A | 12 | a0001c0001t0001g0144a0001c0001t0001g0170a0001c0001t0001g0171others(9): Show | 12 | HG00323.hp2 HG00408.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2624-379_2624-364d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(11): Show |
A | 9 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0030g0092others(6): Show | 9 | HG00738.hp2 HG02723.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.2624-381_2624-364d others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0155a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG00280.hp2 NA18953.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-383_2624-364d others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(15): Show |
A | 1 | a0002c0002t0120g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2624-385_2624-364d others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0023g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2624-389_2624-364d others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0023g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2624-391_2624-364d others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(29): Show |
A | 1 | a0002c0002t0063g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2624-399_2624-364d others(38): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629367
|
ATATATAT others(31): Show |
A | 36 | a0001c0001t0072g0094a0001c0001t0122g0278a0002c0002t0010g0048others(33): Show | 36 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2624-401_2624-364d others(40): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | ||||||
| chr15:55629369
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0035g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2624-381_2624-366d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629369 | ||||||
| chr15:55629369
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0076g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2624-383_2624-366d others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629369 | ||||||
| chr15:55629371
|
A | ATGTG | 4 | a0001c0008t0103g0208a0003c0004t0053g0054a0003c0004t0054g0055others(1): Show | 4 | HG00733.hp2 HG01255.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2624-368_2624-367i others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | ||||||
| chr15:55629371
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0112g0128a0001c0008t0038g0209a0003c0004t0031g0097 | 3 | HG02145.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2624-368_2624-367i others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | ||||||
| chr15:55629371
|
A | ATGTGTGT others(7): Show |
1 | a0001c0008t0083g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2624-368_2624-367i others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | ||||||
| chr15:55629371
|
A | G | 1 | a0003c0004t0032g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2624-367T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | ||||||
| chr15:55629371
|
ATATATG | A | 3 | a0001c0001t0115g0205a0001c0007t0039g0230a0003c0004t0055g0062 | 3 | HG02630.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2624-373_2624-368d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | ||||||
| chr15:55629371
|
ATATATGT others(5): Show |
A | 1 | a0001c0001t0036g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2624-379_2624-368d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | ||||||
| chr15:55629371
|
ATATATGT others(9): Show |
A | 1 | a0006c0011t0036g0220 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2624-383_2624-368d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | ||||||
| chr15:55629373
|
A | ATG | 3 | a0001c0001t0004g0263a0001c0001t0004g0264a0007c0013t0004g0239 | 3 | HG00733.hp1 HG02257.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2624-370_2624-369i others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
A | G | 15 | a0001c0001t0110g0217a0001c0001t0112g0128a0001c0007t0039g0231others(12): Show | 15 | HG00733.hp2 HG01255.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2624-369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATG | A | 3 | a0001c0001t0004g0250a0001c0001t0004g0259a0004c0005t0050g0038 | 3 | HG01358.hp1 HG03490.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2624-373_2624-370d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATGTG | A | 4 | a0001c0001t0002g0249a0001c0001t0004g0258a0004c0006t0009g0007others(1): Show | 4 | HG01515.hp1 HG01517.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-375_2624-370d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATGTGT others(1): Show |
A | 9 | a0001c0001t0002g0248a0001c0001t0034g0102a0001c0001t0040g0132others(6): Show | 9 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.2624-377_2624-370d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATGTGT others(3): Show |
A | 3 | a0001c0001t0002g0251a0001c0001t0034g0101a0002c0002t0114g0215 | 3 | HG01168.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2624-379_2624-370d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATGTGT others(5): Show |
A | 3 | a0001c0001t0004g0281a0001c0001t0004g0282a0001c0001t0033g0098 | 3 | HG02622.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2624-381_2624-370d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATGTGT others(7): Show |
A | 2 | a0001c0001t0033g0103a0001c0001t0109g0232 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2624-383_2624-370d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATGTGT others(15): Show |
A | 1 | a0001c0001t0004g0256 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2624-391_2624-370d others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629373
|
ATATGTGT others(21): Show |
A | 1 | a0009c0015t0044g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2624-397_2624-370d others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | ||||||
| chr15:55629375
|
A | ATG | 8 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0275others(5): Show | 8 | HG00639.hp2 HG01081.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2624-373_2624-372d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
A | ATGTG | 5 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0004g0244others(2): Show | 5 | HG01515.hp2 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2624-375_2624-372d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
A | ATGTGTG | 4 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0270others(1): Show | 4 | HG00741.hp2 HG01943.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-377_2624-372d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0002g0271a0001c0009t0097g0112a0002c0002t0017g0126 | 3 | HG01981.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2624-379_2624-372d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0277 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2624-385_2624-372d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
A | G | 27 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0025g0013others(24): Show | 27 | HG00733.hp1 HG00733.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.2624-371T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
ATG | A | 6 | a0001c0001t0002g0273a0001c0001t0059g0005a0001c0001t0106g0229others(3): Show | 6 | HG01952.hp2 HG02145.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624-373_2624-372d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
ATGTG | A | 3 | a0001c0001t0017g0122a0001c0001t0094g0129a0004c0006t0046g0012 | 3 | HG01358.hp2 HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2624-375_2624-372d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
ATGTGTGT others(3): Show |
A | 1 | a0006c0011t0108g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2624-381_2624-372d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0009t0049g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2624-385_2624-372d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629375
|
ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0056g0004a0001c0001t0057g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2624-387_2624-372d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | ||||||
| chr15:55629379
|
G | A | 2 | a0001c0001t0106g0229a0011c0019t0051g0003 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2624-375C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629379 | ||||||
| chr15:55629381
|
G | A | 1 | a0001c0001t0106g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-377C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629381 | ||||||
| chr15:55629391
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2624-387C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629391 | ||||||
| chr15:55629393
|
G | T | 2 | a0001c0001t0001g0179a0001c0003t0019g0079 | 2 | HG01993.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.2624-389C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629393 | ||||||
| chr15:55629395
|
G | T | 13 | a0001c0001t0001g0134a0001c0001t0001g0151a0001c0001t0001g0158others(10): Show | 13 | HG01074.hp2 HG01975.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2624-391C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629395 | ||||||
| chr15:55629397
|
G | T | 85 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2624-393C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629397 | ||||||
| chr15:55629399
|
G | T | 12 | a0001c0001t0001g0144a0001c0001t0001g0170a0001c0001t0001g0171others(9): Show | 12 | HG00323.hp2 HG00408.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2624-395C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629399 | ||||||
| chr15:55629401
|
G | T | 9 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0030g0092others(6): Show | 9 | HG00738.hp2 HG02723.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.2624-397C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629401 | ||||||
| chr15:55629403
|
G | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG00280.hp2 NA18953.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-399C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629403 | ||||||
| chr15:55629405
|
G | A | 1 | a0002c0002t0074g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-401C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629405 | ||||||
| chr15:55629405
|
G | T | 1 | a0002c0002t0120g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2624-401C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629405 | ||||||
| chr15:55629537
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2624-533G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629537 | ||||||
| chr15:55629694
|
T | C | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2624-690A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629694 | ||||||
| chr15:55629790
|
G | T | 128 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.2624-786C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629790 | ||||||
| chr15:55629795
|
CATGAATA others(1): Show |
C | 127 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2624-799_2624-792d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629795 | ||||||
| chr15:55629858
|
G | A | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2624-854C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629858 | ||||||
| chr15:55629881
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0206a0001c0001t0008g0207 | 3 | NA18948.hp2 NA18980.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2624-877C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629881 | ||||||
| chr15:55629936
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-932G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629936 | ||||||
| chr15:55629984
|
A | AT | 12 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0001g0226others(9): Show | 12 | HG01074.hp1 HG01934.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2624-981dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629984 | ||||||
| chr15:55629984
|
AT | A | 9 | a0001c0001t0002g0248a0001c0001t0004g0244a0001c0001t0004g0263others(6): Show | 10 | HG01515.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2624-981delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629984 | ||||||
| chr15:55629985
|
T | C | 1 | a0001c0009t0049g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2624-981A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629985 | ||||||
| chr15:55630110
|
C | T | 1 | a0002c0002t0074g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-1106G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630110 | ||||||
| chr15:55630118
|
C | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2624-1114G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630118 | ||||||
| chr15:55630207
|
C | T | 4 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2624-1203G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630207 | ||||||
| chr15:55630245
|
C | G | 1 | a0001c0001t0005g0141 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2624-1241G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630245 | ||||||
| chr15:55630263
|
G | C | 38 | a0001c0001t0072g0094a0001c0001t0122g0278a0002c0002t0010g0048others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2624-1259C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630263 | ||||||
| chr15:55630281
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2624-1277G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630281 | ||||||
| chr15:55630389
|
C | T | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.2624-1385G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630389 | ||||||
| chr15:55630468
|
G | T | 2 | a0001c0001t0023g0051a0001c0001t0023g0058 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2624-1464C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630468 | ||||||
| chr15:55630469
|
C | T | 2 | a0001c0001t0023g0051a0001c0001t0023g0058 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2624-1465G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630469 | ||||||
| chr15:55630571
|
A | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-1567T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630571 | ||||||
| chr15:55630573
|
T | A | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-1569A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630573 | ||||||
| chr15:55630687
|
T | G | 1 | a0002c0002t0007g0070 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2624-1683A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630687 | ||||||
| chr15:55630698
|
T | C | 1 | a0002c0002t0062g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2624-1694A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630698 | ||||||
| chr15:55630918
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2624-1914A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630918 | ||||||
| chr15:55630940
|
T | C | 1 | a0001c0001t0011g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2624-1936A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630940 | ||||||
| chr15:55631198
|
G | C | 1 | a0001c0001t0015g0140 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2624-2194C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631198 | ||||||
| chr15:55631266
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2624-2262G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631266 | ||||||
| chr15:55631465
|
C | T | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2624-2461G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631465 | ||||||
| chr15:55631710
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-2706C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631710 | ||||||
| chr15:55631757
|
C | T | 61 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2624-2753G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631757 | ||||||
| chr15:55631768
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-2764A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631768 | ||||||
| chr15:55631870
|
G | A | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2624-2866C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631870 | ||||||
| chr15:55632074
|
A | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-3070T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632074 | ||||||
| chr15:55632250
|
T | C | 39 | a0001c0001t0002g0277a0001c0001t0072g0094a0001c0001t0122g0278others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2624-3246A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632250 | ||||||
| chr15:55632277
|
T | C | 1 | a0001c0001t0106g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-3273A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632277 | ||||||
| chr15:55632316
|
T | G | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2624-3312A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632316 | ||||||
| chr15:55632411
|
T | C | 140 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2624-3407A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632411 | ||||||
| chr15:55632485
|
T | A | 1 | a0001c0001t0019g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2624-3481A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632485 | ||||||
| chr15:55632521
|
T | A | 1 | a0006c0011t0104g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2624-3517A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632521 | ||||||
| chr15:55632558
|
A | C | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-3554T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632558 | ||||||
| chr15:55632666
|
A | G | 1 | a0002c0002t0074g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-3662T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632666 | ||||||
| chr15:55632702
|
G | A | 1 | a0002c0002t0012g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2624-3698C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632702 | ||||||
| chr15:55632755
|
G | C | 6 | a0003c0004t0024g0056a0003c0004t0024g0057a0003c0004t0052g0059others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2624-3751C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632755 | ||||||
| chr15:55632828
|
G | A | 274 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.2624-3824C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632828 | ||||||
| chr15:55632881
|
G | A | 1 | a0001c0009t0097g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2624-3877C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632881 | ||||||
| chr15:55632899
|
T | A | 1 | a0001c0020t0058g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2624-3895A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632899 | ||||||
| chr15:55632906
|
G | A | 1 | a0001c0001t0041g0135 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2624-3902C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632906 | ||||||
| chr15:55633191
|
T | G | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2623+3979A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633191 | ||||||
| chr15:55633242
|
C | CT | 10 | a0001c0001t0036g0218a0001c0001t0059g0005a0001c0001t0112g0128others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2623+3927dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633242 | ||||||
| chr15:55633447
|
T | C | 274 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.2623+3723A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633447 | ||||||
| chr15:55633463
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2623+3707G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633463 | ||||||
| chr15:55633631
|
G | A | 20 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2623+3539C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633631 | ||||||
| chr15:55633749
|
G | A | 76 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2623+3421C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633749 | ||||||
| chr15:55633849
|
C | T | 1 | a0001c0007t0116g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2623+3321G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633849 | ||||||
| chr15:55633956
|
T | C | 42 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0035g0001others(39): Show | 43 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2623+3214A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633956 | ||||||
| chr15:55633965
|
C | T | 42 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0035g0001others(39): Show | 43 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2623+3205G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633965 | ||||||
| chr15:55633976
|
T | C | 40 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0072g0094others(37): Show | 40 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.2623+3194A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633976 | ||||||
| chr15:55634063
|
C | CTT | 36 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0072g0094others(33): Show | 36 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2623+3105_2623+310 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634063 | ||||||
| chr15:55634063
|
CT | C | 201 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2623+3106delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634063 | ||||||
| chr15:55634063
|
CTT | C | 13 | a0001c0001t0001g0131a0001c0001t0001g0177a0001c0001t0002g0249others(10): Show | 13 | HG01074.hp1 HG01975.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2623+3105_2623+310 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634063 | ||||||
| chr15:55634213
|
G | A | 20 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2623+2957C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634213 | ||||||
| chr15:55634225
|
G | A | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.2623+2945C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634225 | ||||||
| chr15:55634427
|
C | T | 1 | a0001c0020t0058g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2623+2743G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634427 | ||||||
| chr15:55634535
|
T | C | 48 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.2623+2635A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634535 | ||||||
| chr15:55634735
|
G | A | 49 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.2623+2435C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634735 | ||||||
| chr15:55634831
|
C | G | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2623+2339G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634831 | ||||||
| chr15:55634899
|
G | A | 49 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0144others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.2623+2271C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634899 | ||||||
| chr15:55634902
|
T | C | 168 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2623+2268A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634902 | ||||||
| chr15:55634947
|
GCCATGTA others(11): Show |
G | 1 | a0001c0008t0038g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2623+2205_2623+222 others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634947 | ||||||
| chr15:55634949
|
C | G | 1 | a0002c0002t0003g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2623+2221G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634949 | ||||||
| chr15:55635051
|
G | A | 6 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623+2119C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635051 | ||||||
| chr15:55635061
|
G | C | 274 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.2623+2109C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635061 | ||||||
| chr15:55635069
|
T | TTC | 6 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(3): Show | 6 | HG02145.hp1 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623+2099_2623+210 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635069 | ||||||
| chr15:55635071
|
C | CTG | 4 | a0001c0001t0030g0092a0001c0003t0003g0080a0011c0019t0051g0003others(1): Show | 4 | HG02300.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+2097_2623+209 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(1): Show |
6 | a0001c0009t0049g0035a0004c0005t0022g0039a0004c0005t0022g0041others(3): Show | 6 | HG00741.hp1 HG01106.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(3): Show |
7 | a0001c0001t0004g0255a0001c0001t0059g0005a0001c0001t0106g0229others(4): Show | 7 | HG00140.hp1 HG01517.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(5): Show |
35 | a0001c0001t0001g0196a0001c0001t0002g0240a0001c0001t0002g0241others(32): Show | 35 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(7): Show |
53 | a0001c0001t0001g0115a0001c0001t0001g0130a0001c0001t0001g0131others(50): Show | 53 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(9): Show |
27 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0134others(24): Show | 27 | HG01074.hp2 HG01891.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(11): Show |
5 | a0001c0001t0001g0200a0001c0001t0004g0281a0001c0001t0004g0282others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(13): Show |
4 | a0001c0001t0002g0249a0001c0001t0034g0102a0001c0001t0040g0166others(1): Show | 4 | HG01975.hp1 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
C | CTGTGTGT others(15): Show |
4 | a0001c0001t0002g0257a0001c0001t0033g0098a0001c0001t0033g0103others(1): Show | 4 | HG02273.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
CTGGGTGT others(1): Show |
C | 3 | a0001c0001t0035g0001a0001c0001t0076g0133a0002c0002t0070g0017 | 4 | HG03491.hp2 HG03492.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+2091_2623+209 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635071
|
CTGGGTGT others(3): Show |
C | 51 | a0001c0001t0001g0171a0001c0001t0001g0176a0001c0001t0001g0178others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2623+2089_2623+209 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | ||||||
| chr15:55635073
|
G | C | 14 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(11): Show | 14 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+2097C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635073 | ||||||
| chr15:55635074
|
G | T | 218 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2623+2096C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635074 | ||||||
| chr15:55635103
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0090g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2623+2066_2623+206 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635103 | ||||||
| chr15:55635104
|
T | TGTGTGTG others(8): Show |
3 | a0001c0001t0001g0144a0001c0001t0001g0179a0001c0001t0085g0147 | 3 | HG01993.hp2 HG03669.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2623+2065_2623+206 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635104 | ||||||
| chr15:55635105
|
T | G | 65 | a0001c0001t0001g0155a0001c0001t0001g0186a0001c0001t0023g0051others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2623+2065A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635105 | ||||||
| chr15:55635124
|
C | T | 44 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0072g0094others(41): Show | 44 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.2623+2046G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635124 | ||||||
| chr15:55635216
|
C | T | 1 | a0006c0011t0104g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2623+1954G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635216 | ||||||
| chr15:55635217
|
G | A | 38 | a0001c0001t0072g0094a0001c0001t0122g0278a0002c0002t0010g0048others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2623+1953C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635217 | ||||||
| chr15:55635223
|
T | C | 268 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2623+1947A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635223 | ||||||
| chr15:55635235
|
G | C | 4 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(1): Show | 4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+1935C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635235 | ||||||
| chr15:55635423
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2623+1747T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635423 | ||||||
| chr15:55635451
|
G | A | 3 | a0001c0001t0023g0051a0001c0001t0023g0058a0002c0002t0063g0047 | 3 | HG02559.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2623+1719C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635451 | ||||||
| chr15:55635500
|
T | C | 138 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2623+1670A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635500 | ||||||
| chr15:55635521
|
A | G | 1 | a0002c0002t0017g0126 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2623+1649T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635521 | ||||||
| chr15:55635563
|
T | C | 1 | a0001c0001t0004g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2623+1607A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635563 | ||||||
| chr15:55635733
|
A | G | 11 | a0003c0004t0024g0056a0003c0004t0024g0057a0003c0004t0031g0097others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2623+1437T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635733 | ||||||
| chr15:55635934
|
C | T | 50 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.2623+1236G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635934 | ||||||
| chr15:55636057
|
G | T | 1 | a0001c0001t0059g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2623+1113C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636057 | ||||||
| chr15:55636074
|
T | G | 79 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2623+1096A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636074 | ||||||
| chr15:55636369
|
C | T | 1 | a0001c0001t0111g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2623+801G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636369 | ||||||
| chr15:55636478
|
T | A | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2623+692A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636478 | ||||||
| chr15:55636578
|
G | C | 1 | a0002c0002t0012g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2623+592C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636578 | ||||||
| chr15:55636849
|
G | T | 6 | a0003c0004t0024g0056a0003c0004t0024g0057a0003c0004t0052g0059others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2623+321C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636849 | ||||||
| chr15:55636871
|
T | A | 1 | a0014c0018t0015g0189 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2623+299A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636871 | ||||||
| chr15:55636929
|
G | C | 25 | a0002c0002t0010g0048a0002c0002t0010g0049a0002c0002t0010g0050others(22): Show | 25 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2623+241C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636929 | ||||||
| chr15:55637087
|
A | G | 4 | a0001c0001t0004g0255a0001c0001t0004g0259a0001c0001t0004g0263others(1): Show | 4 | HG00733.hp1 HG01517.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+83T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637087 | ||||||
| chr15:55637110
|
T | C | 2 | a0002c0002t0003g0066a0002c0002t0003g0071 | 2 | NA18963.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2623+60A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637110 | ||||||
| chr15:55637129
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2623+41T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637129 | ||||||
| chr15:55637140
|
T | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2623+30A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637140 | ||||||
| chr15:55637452
|
G | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2453-112C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55637452 | ||||||
| chr15:55637996
|
G | T | 1 | a0012c0017t0002g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2452+553C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55637996 | ||||||
| chr15:55638028
|
T | C | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2452+521A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638028 | ||||||
| chr15:55638033
|
T | C | 50 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.2452+516A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638033 | ||||||
| chr15:55638042
|
T | C | 1 | a0004c0005t0047g0037 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2452+507A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638042 | ||||||
| chr15:55638047
|
C | A | 20 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2452+502G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638047 | ||||||
| chr15:55638051
|
G | A | 1 | a0001c0001t0040g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2452+498C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638051 | ||||||
| chr15:55638170
|
T | C | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2452+379A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638170 | ||||||
| chr15:55638180
|
A | G | 1 | a0001c0009t0097g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2452+369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638180 | ||||||
| chr15:55638337
|
G | A | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.2452+212C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638337 | ||||||
| chr15:55638344
|
C | T | 143 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.2452+205G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638344 | ||||||
| chr15:55638379
|
A | T | 144 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2452+170T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638379 | ||||||
| chr15:55638528
|
A | G | 1 | a0001c0001t0041g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2452+21T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638528 | ||||||
| chr15:55638826
|
T | C | 1 | a0001c0001t0115g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2325-150A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638826 | ||||||
| chr15:55638928
|
G | T | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2325-252C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638928 | ||||||
| chr15:55638955
|
A | ATCAT | 76 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0257others(73): Show | 77 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2325-283_2325-280d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | ||||||
| chr15:55638955
|
A | ATCATTCA others(1): Show |
3 | a0001c0001t0109g0232a0002c0002t0012g0016a0011c0019t0051g0003 | 3 | HG02683.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2325-287_2325-280d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | ||||||
| chr15:55638955
|
A | ATCATTCA others(5): Show |
1 | a0001c0001t0106g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2325-291_2325-280d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | ||||||
| chr15:55638955
|
ATCAT | A | 149 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2325-283_2325-280d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | ||||||
| chr15:55638955
|
ATCATTCA others(5): Show |
A | 1 | a0001c0001t0111g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2325-291_2325-280d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | ||||||
| chr15:55638963
|
T | A | 9 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(6): Show | 9 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2325-287A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638963 | ||||||
| chr15:55639007
|
T | C | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-331A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639007 | ||||||
| chr15:55639070
|
C | G | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-394G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639070 | ||||||
| chr15:55639085
|
T | C | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-409A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639085 | ||||||
| chr15:55639149
|
T | A | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-473A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639149 | ||||||
| chr15:55639407
|
T | C | 1 | a0010c0014t0079g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2324+235A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639407 | ||||||
| chr15:55639507
|
C | T | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2324+135G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639507 | ||||||
| chr15:55639518
|
T | G | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2324+124A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639518 | ||||||
| chr15:55639861
|
G | A | 1 | a0001c0001t0085g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2138-33C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55639861 | ||||||
| chr15:55639989
|
C | G | 76 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2138-161G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55639989 | ||||||
| chr15:55640029
|
T | A | 1 | a0001c0001t0043g0272 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2138-201A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640029 | ||||||
| chr15:55640069
|
T | C | 1 | a0002c0002t0027g0029 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2138-241A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640069 | ||||||
| chr15:55640108
|
C | CAG | 10 | a0001c0001t0036g0218a0001c0001t0059g0005a0001c0001t0112g0128others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2138-282_2138-281d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640108 | ||||||
| chr15:55640191
|
A | G | 1 | a0003c0004t0031g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2138-363T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640191 | ||||||
| chr15:55640419
|
T | C | 189 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.2138-591A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640419 | ||||||
| chr15:55640427
|
A | G | 11 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2138-599T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640427 | ||||||
| chr15:55640567
|
G | A | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2137+546C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640567 | ||||||
| chr15:55640688
|
CTTAAATA others(20): Show |
C | 1 | a0001c0001t0090g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2137+398_2137+424d others(29): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640688 | ||||||
| chr15:55640727
|
T | C | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2137+386A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640727 | ||||||
| chr15:55640791
|
C | G | 60 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(57): Show | 60 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.2137+322G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640791 | ||||||
| chr15:55640856
|
C | CA | 46 | a0001c0001t0004g0256a0001c0001t0023g0051a0001c0001t0023g0058others(43): Show | 47 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2137+256dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640856 | ||||||
| chr15:55640967
|
A | C | 1 | a0001c0001t0008g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2137+146T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640967 | ||||||
| chr15:55641001
|
G | T | 145 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.2137+112C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55641001 | ||||||
| chr15:55641033
|
T | C | 1 | a0001c0009t0049g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2137+80A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55641033 | ||||||
| chr15:55641231
|
T | C | 15 | a0001c0001t0072g0094a0001c0001t0122g0278a0002c0002t0020g0052others(12): Show | 15 | HG00323.hp1 HG01071.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2042-23A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641231 | ||||||
| chr15:55641354
|
A | C | 2 | a0001c0001t0023g0051a0001c0001t0023g0058 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2042-146T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641354 | ||||||
| chr15:55641371
|
T | C | 1 | a0001c0001t0005g0141 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2042-163A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641371 | ||||||
| chr15:55641459
|
C | T | 1 | a0001c0001t0004g0255 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2042-251G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641459 | ||||||
| chr15:55641539
|
G | A | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2042-331C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641539 | ||||||
| chr15:55641771
|
A | T | 48 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.2042-563T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641771 | ||||||
| chr15:55641857
|
C | A | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-649G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641857 | ||||||
| chr15:55641939
|
C | A | 5 | a0001c0001t0036g0218a0001c0001t0112g0128a0001c0012t0078g0113others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-731G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641939 | ||||||
| chr15:55641977
|
A | T | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-769T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641977 | ||||||
| chr15:55641989
|
A | G | 8 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0092g0127others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2042-781T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641989 | ||||||
| chr15:55642101
|
G | A | 3 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0047g0037 | 3 | HG00099.hp1 HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2042-893C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642101 | ||||||
| chr15:55642136
|
T | TGCAGTCC | 27 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005others(24): Show | 27 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.2042-935_2042-929d others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642136 | ||||||
| chr15:55642159
|
C | T | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-951G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642159 | ||||||
| chr15:55642180
|
C | CA | 38 | a0001c0001t0001g0151a0001c0001t0001g0173a0001c0001t0001g0178others(35): Show | 38 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.2042-973dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | ||||||
| chr15:55642180
|
C | CAA | 8 | a0001c0001t0002g0270a0001c0001t0057g0006a0002c0002t0005g0117others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-974_2042-973d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | ||||||
| chr15:55642180
|
CA | C | 53 | a0001c0001t0001g0130a0001c0001t0014g0154a0001c0001t0014g0167others(50): Show | 53 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.2042-973delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | ||||||
| chr15:55642180
|
CAA | C | 11 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0035g0001others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2042-974_2042-973d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | ||||||
| chr15:55642192
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0110g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2042-996_2042-985d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642192 | ||||||
| chr15:55642203
|
AT | A | 3 | a0002c0002t0120g0236a0004c0006t0009g0015a0009c0015t0044g0011 | 3 | HG00733.hp2 HG03239.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-996delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642203 | ||||||
| chr15:55642204
|
T | A | 31 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0007t0039g0230others(28): Show | 31 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.2042-996A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642204 | ||||||
| chr15:55642207
|
T | G | 23 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0110g0217others(20): Show | 23 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2042-999A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642207 | ||||||
| chr15:55642315
|
G | C | 63 | a0001c0001t0005g0141a0001c0001t0005g0164a0001c0001t0011g0075others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2042-1107C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642315 | ||||||
| chr15:55642381
|
C | G | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-1173G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642381 | ||||||
| chr15:55642579
|
C | G | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-1371G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642579 | ||||||
| chr15:55642597
|
CA | C | 158 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0130others(155): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2042-1390delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642597 | ||||||
| chr15:55642597
|
CAA | C | 10 | a0001c0001t0001g0106a0001c0001t0002g0261a0001c0001t0002g0277others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2042-1391_2042-139 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642597 | ||||||
| chr15:55642642
|
T | C | 5 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(2): Show | 5 | HG00741.hp2 HG01106.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-1434A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642642 | ||||||
| chr15:55642812
|
G | A | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2042-1604C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642812 | ||||||
| chr15:55642858
|
G | A | 1 | a0002c0002t0120g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2042-1650C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642858 | ||||||
| chr15:55643079
|
AAACT | A | 5 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0093g0125others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-1875_2042-187 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643079 | ||||||
| chr15:55643134
|
G | C | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-1926C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643134 | ||||||
| chr15:55643293
|
G | A | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2042-2085C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643293 | ||||||
| chr15:55643297
|
G | A | 1 | a0001c0008t0103g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2042-2089C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643297 | ||||||
| chr15:55643558
|
C | G | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-2350G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643558 | ||||||
| chr15:55643689
|
G | A | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2042-2481C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643689 | ||||||
| chr15:55643864
|
A | AT | 7 | a0001c0001t0004g0256a0001c0001t0036g0218a0001c0001t0089g0202others(4): Show | 7 | HG02040.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042-2657dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643864 | ||||||
| chr15:55643901
|
C | A | 2 | a0001c0001t0056g0004a0001c0001t0057g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2042-2693G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643901 | ||||||
| chr15:55643904
|
C | T | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-2696G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643904 | ||||||
| chr15:55643910
|
C | A | 3 | a0001c0001t0030g0092a0002c0002t0120g0236a0013c0016t0030g0093 | 3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-2702G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643910 | ||||||
| chr15:55644040
|
C | T | 269 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2042-2832G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644040 | ||||||
| chr15:55644126
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2042-2918T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644126 | ||||||
| chr15:55644151
|
T | C | 1 | a0001c0001t0019g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2042-2943A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644151 | ||||||
| chr15:55644391
|
T | A | 4 | a0001c0001t0004g0255a0001c0001t0004g0259a0001c0001t0004g0263others(1): Show | 4 | HG00733.hp1 HG01517.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-3183A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644391 | ||||||
| chr15:55644421
|
G | C | 5 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0035g0001others(2): Show | 6 | HG02809.hp2 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-3213C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644421 | ||||||
| chr15:55644643
|
C | T | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-3435G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644643 | ||||||
| chr15:55644737
|
G | A | 125 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(122): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2042-3529C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644737 | ||||||
| chr15:55644742
|
A | G | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-3534T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644742 | ||||||
| chr15:55644833
|
G | C | 39 | a0001c0001t0072g0094a0001c0001t0122g0278a0002c0002t0010g0048others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2042-3625C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644833 | ||||||
| chr15:55644862
|
A | C | 1 | a0002c0002t0003g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2042-3654T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644862 | ||||||
| chr15:55644972
|
C | T | 1 | a0001c0001t0008g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2042-3764G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644972 | ||||||
| chr15:55645164
|
G | A | 60 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(57): Show | 60 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.2042-3956C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645164 | ||||||
| chr15:55645201
|
C | T | 9 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(6): Show | 9 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2042-3993G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645201 | ||||||
| chr15:55645202
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0144 | 2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2042-3994C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645202 | ||||||
| chr15:55645210
|
C | T | 5 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-4002G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645210 | ||||||
| chr15:55645226
|
G | C | 2 | a0001c0001t0041g0135a0001c0001t0041g0136 | 2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2042-4018C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645226 | ||||||
| chr15:55645304
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0245 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2042-4096G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645304 | ||||||
| chr15:55645374
|
C | G | 45 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.2042-4166G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645374 | ||||||
| chr15:55645388
|
C | T | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-4180G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645388 | ||||||
| chr15:55645433
|
C | CA | 6 | a0001c0001t0059g0005a0001c0009t0049g0035a0001c0009t0097g0112others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-4226dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAA | 14 | a0001c0001t0035g0001a0001c0001t0076g0133a0002c0002t0015g0227others(11): Show | 15 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.2042-4230_2042-422 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(2): Show |
11 | a0001c0001t0023g0058a0003c0004t0024g0056a0003c0004t0024g0057others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2042-4234_2042-422 others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0176a0001c0001t0001g0185a0001c0001t0016g0116others(3): Show | 6 | HG00639.hp1 HG01256.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2042-4235_2042-422 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0005g0141a0001c0001t0025g0030a0001c0001t0030g0092others(3): Show | 6 | HG01433.hp2 HG02015.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-4236_2042-422 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(5): Show |
32 | a0001c0001t0004g0247a0001c0001t0005g0164a0001c0001t0011g0075others(29): Show | 32 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2042-4237_2042-422 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(6): Show |
14 | a0001c0001t0041g0135a0001c0001t0077g0142a0001c0003t0005g0225others(11): Show | 14 | HG02027.hp1 HG02027.hp2 HG04228.hp2 others(11): Show |
intron_variant | MODIFIER | c.2042-4238_2042-422 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0270a0001c0001t0002g0274a0002c0002t0011g0084 | 3 | HG01943.hp2 HG01993.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2042-4239_2042-422 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(8): Show |
1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2042-4240_2042-422 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0106a0001c0001t0002g0273a0001c0001t0008g0152others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(23): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(13): Show |
35 | a0001c0001t0001g0107a0001c0001t0001g0131a0001c0001t0001g0173others(32): Show | 35 | HG00280.hp2 HG00408.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(14): Show |
33 | a0001c0001t0001g0130a0001c0001t0001g0144a0001c0001t0001g0149others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(25): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(15): Show |
12 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0155others(9): Show | 12 | HG00738.hp1 HG01071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(16): Show |
5 | a0001c0001t0001g0138a0001c0001t0001g0181a0001c0001t0002g0251others(2): Show | 5 | HG01168.hp1 HG02257.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(27): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(17): Show |
17 | a0001c0001t0001g0199a0001c0001t0002g0242a0001c0001t0002g0248others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(18): Show |
14 | a0001c0001t0002g0241a0001c0001t0002g0245a0001c0001t0002g0246others(11): Show | 14 | HG00140.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(29): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(19): Show |
7 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(4): Show | 7 | HG01256.hp2 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(20): Show |
2 | a0001c0001t0002g0238a0001c0001t0002g0268 | 2 | HG01258.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(31): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0002g0261a0001c0001t0043g0260 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(33): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645433
|
C | CAAAAAAA others(23): Show |
2 | a0001c0001t0002g0240a0011c0019t0051g0003 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(34): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | ||||||
| chr15:55645511
|
G | C | 10 | a0001c0001t0036g0218a0001c0001t0059g0005a0001c0001t0112g0128others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2042-4303C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645511 | ||||||
| chr15:55645785
|
C | T | 1 | a0001c0001t0008g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2042-4577G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645785 | ||||||
| chr15:55645824
|
C | T | 1 | a0001c0007t0039g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2042-4616G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645824 | ||||||
| chr15:55645848
|
G | C | 9 | a0001c0001t0036g0218a0001c0008t0038g0209a0001c0008t0038g0210others(6): Show | 9 | HG02572.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2042-4640C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645848 | ||||||
| chr15:55645909
|
A | C | 6 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(3): Show | 6 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2042-4701T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645909 | ||||||
| chr15:55646015
|
T | A | 2 | a0001c0001t0056g0004a0001c0001t0057g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2042-4807A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646015 | ||||||
| chr15:55646081
|
A | ACCGCAAC others(9): Show |
2 | a0001c0001t0084g0192a0001c0003t0018g0090 | 2 | HG00408.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2042-4889_2042-487 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646081 | ||||||
| chr15:55646173
|
G | GT | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2042-4966dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646173 | ||||||
| chr15:55646173
|
G | GTT | 6 | a0001c0001t0014g0167a0001c0001t0040g0166a0001c0001t0119g0160others(3): Show | 6 | HG01109.hp1 HG01978.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-4967_2042-496 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646173 | ||||||
| chr15:55646173
|
GT | G | 31 | a0001c0001t0001g0171a0001c0001t0001g0187a0001c0001t0005g0164others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.2042-4966delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646173 | ||||||
| chr15:55646175
|
T | G | 1 | a0001c0001t0111g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2042-4967A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646175 | ||||||
| chr15:55646182
|
T | G | 5 | a0001c0001t0036g0218a0001c0012t0078g0113a0002c0002t0028g0021others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-4974A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646182 | ||||||
| chr15:55646292
|
A | G | 64 | a0001c0001t0001g0150a0001c0001t0001g0177a0001c0001t0001g0226others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.2042-5084T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646292 | ||||||
| chr15:55646325
|
CTCT | C | 12 | a0001c0001t0033g0098a0003c0004t0024g0056a0003c0004t0024g0057others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2042-5120_2042-511 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646325 | ||||||
| chr15:55646327
|
C | CT | 16 | a0001c0001t0001g0151a0001c0001t0023g0051a0001c0001t0023g0058others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.2042-5120dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646327 | ||||||
| chr15:55646346
|
G | A | 1 | a0001c0008t0103g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2042-5138C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646346 | ||||||
| chr15:55646351
|
C | T | 2 | a0001c0007t0039g0230a0001c0007t0039g0231 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2042-5143G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646351 | ||||||
| chr15:55646423
|
C | T | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2042-5215G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646423 | ||||||
| chr15:55646456
|
A | C | 4 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005others(1): Show | 4 | HG01891.hp2 HG02818.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2042-5248T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646456 | ||||||
| chr15:55646456
|
A | G | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2042-5248T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646456 | ||||||
| chr15:55646468
|
G | A | 43 | a0001c0001t0033g0103a0001c0001t0034g0101a0001c0001t0034g0102others(40): Show | 43 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2042-5260C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646468 | ||||||
| chr15:55646478
|
A | G | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2042-5270T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646478 | ||||||
| chr15:55646479
|
C | T | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2042-5271G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646479 | ||||||
| chr15:55646480
|
G | A | 14 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2042-5272C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646480 | ||||||
| chr15:55646499
|
T | C | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-5291A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646499 | ||||||
| chr15:55646554
|
C | G | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-5346G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646554 | ||||||
| chr15:55646569
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0187a0001c0001t0088g0194 | 3 | HG00280.hp2 HG02486.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2042-5361C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646569 | ||||||
| chr15:55646634
|
T | C | 1 | a0002c0002t0003g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2042-5426A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646634 | ||||||
| chr15:55646656
|
G | C | 1 | a0001c0001t0115g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2042-5448C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646656 | ||||||
| chr15:55646681
|
T | C | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-5473A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646681 | ||||||
| chr15:55646685
|
G | A | 1 | a0001c0001t0087g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2042-5477C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646685 | ||||||
| chr15:55646714
|
A | G | 39 | a0001c0001t0122g0278a0002c0002t0010g0048a0002c0002t0010g0049others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2042-5506T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646714 | ||||||
| chr15:55646863
|
A | C | 1 | a0002c0002t0062g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2042-5655T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646863 | ||||||
| chr15:55646922
|
C | T | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-5714G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646922 | ||||||
| chr15:55647153
|
G | A | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2042-5945C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647153 | ||||||
| chr15:55647388
|
G | C | 39 | a0001c0001t0122g0278a0002c0002t0010g0048a0002c0002t0010g0049others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2042-6180C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647388 | ||||||
| chr15:55647503
|
T | G | 3 | a0001c0001t0001g0196a0001c0001t0086g0197a0001c0001t0111g0228 | 3 | HG02976.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2042-6295A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647503 | ||||||
| chr15:55647695
|
G | A | 1 | a0001c0009t0049g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2042-6487C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647695 | ||||||
| chr15:55647761
|
A | G | 63 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(60): Show |
intron_variant | MODIFIER | c.2042-6553T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647761 | ||||||
| chr15:55647778
|
T | C | 2 | a0001c0009t0113g0233a0010c0014t0079g0234 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2042-6570A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647778 | ||||||
| chr15:55647923
|
G | C | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-6715C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647923 | ||||||
| chr15:55647989
|
G | A | 1 | a0001c0007t0039g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2042-6781C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647989 | ||||||
| chr15:55648002
|
C | A | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-6794G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648002 | ||||||
| chr15:55648041
|
C | T | 1 | a0005c0010t0064g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2042-6833G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648041 | ||||||
| chr15:55648219
|
A | G | 2 | a0001c0001t0023g0051a0001c0001t0023g0058 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2042-7011T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648219 | ||||||
| chr15:55648274
|
G | A | 6 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(3): Show | 6 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2042-7066C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648274 | ||||||
| chr15:55648468
|
A | AT | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-7261dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648468 | ||||||
| chr15:55648510
|
G | A | 1 | a0016c0023t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2042-7302C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648510 | ||||||
| chr15:55648512
|
C | T | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-7304G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648512 | ||||||
| chr15:55648533
|
A | T | 3 | a0001c0012t0078g0113a0001c0012t0080g0114a0011c0019t0051g0003 | 3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2042-7325T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648533 | ||||||
| chr15:55648619
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2042-7411A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648619 | ||||||
| chr15:55648631
|
C | G | 1 | a0002c0002t0026g0078 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2042-7423G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648631 | ||||||
| chr15:55648659
|
A | G | 3 | a0001c0012t0078g0113a0001c0012t0080g0114a0011c0019t0051g0003 | 3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2042-7451T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648659 | ||||||
| chr15:55648778
|
C | T | 17 | a0002c0002t0012g0016a0002c0002t0012g0018a0002c0002t0012g0028others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2042-7570G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648778 | ||||||
| chr15:55648793
|
A | G | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-7585T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648793 | ||||||
| chr15:55649000
|
C | G | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2042-7792G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649000 | ||||||
| chr15:55649088
|
C | CA | 47 | a0001c0001t0001g0182a0001c0001t0001g0226a0001c0001t0002g0238others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.2042-7881dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649088 | ||||||
| chr15:55649105
|
A | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-7897T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649105 | ||||||
| chr15:55649336
|
T | C | 4 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0187others(1): Show | 4 | HG00280.hp2 HG01934.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-8128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649336 | ||||||
| chr15:55649427
|
C | CA | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2042-8220_2042-821 others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649427 | ||||||
| chr15:55649458
|
C | T | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2042-8250G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649458 | ||||||
| chr15:55649643
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2042-8435G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649643 | ||||||
| chr15:55649762
|
G | A | 17 | a0002c0002t0012g0016a0002c0002t0012g0018a0002c0002t0012g0028others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2042-8554C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649762 | ||||||
| chr15:55649791
|
C | CAATA | 8 | a0001c0001t0084g0192a0001c0001t0112g0128a0001c0003t0003g0042others(5): Show | 8 | HG00408.hp2 HG01943.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-8587_2042-858 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | ||||||
| chr15:55649791
|
CAATA | C | 11 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0041g0135others(8): Show | 11 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.2042-8587_2042-858 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | ||||||
| chr15:55649791
|
CAATAAAT others(1): Show |
C | 41 | a0001c0001t0001g0165a0001c0001t0030g0092a0001c0001t0056g0004others(38): Show | 41 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2042-8591_2042-858 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | ||||||
| chr15:55649791
|
CAATAAAT others(5): Show |
C | 176 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.2042-8595_2042-858 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | ||||||
| chr15:55649907
|
T | C | 1 | a0002c0002t0011g0084 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2042-8699A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649907 | ||||||
| chr15:55650038
|
T | G | 1 | a0001c0001t0076g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2042-8830A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650038 | ||||||
| chr15:55650084
|
T | G | 14 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2042-8876A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650084 | ||||||
| chr15:55650130
|
T | C | 1 | a0002c0002t0027g0029 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2042-8922A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650130 | ||||||
| chr15:55650276
|
T | C | 1 | a0002c0002t0021g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2042-9068A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650276 | ||||||
| chr15:55650374
|
G | C | 205 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(202): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.2042-9166C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650374 | ||||||
| chr15:55650757
|
G | C | 1 | a0001c0001t0017g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2042-9549C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650757 | ||||||
| chr15:55651001
|
C | G | 13 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.2042-9793G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651001 | ||||||
| chr15:55651086
|
A | G | 1 | a0001c0001t0014g0154 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2042-9878T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651086 | ||||||
| chr15:55651344
|
A | G | 181 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2042-10136T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651344 | ||||||
| chr15:55651375
|
G | A | 1 | a0003c0004t0031g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2042-10167C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651375 | ||||||
| chr15:55651648
|
G | A | 1 | a0002c0002t0061g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2042-10440C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651648 | ||||||
| chr15:55651669
|
A | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-10461T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651669 | ||||||
| chr15:55652031
|
T | C | 1 | a0005c0010t0026g0065 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2042-10823A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652031 | ||||||
| chr15:55652113
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2042-10905G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652113 | ||||||
| chr15:55652125
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-10917G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652125 | ||||||
| chr15:55652194
|
G | A | 5 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(2): Show | 5 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-10986C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652194 | ||||||
| chr15:55652319
|
G | A | 86 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2042-11111C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652319 | ||||||
| chr15:55652349
|
A | G | 1 | a0001c0001t0004g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2042-11141T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652349 | ||||||
| chr15:55652460
|
G | A | 1 | a0005c0010t0026g0065 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2042-11252C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652460 | ||||||
| chr15:55652708
|
G | A | 1 | a0001c0001t0106g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2042-11500C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652708 | ||||||
| chr15:55652872
|
G | A | 1 | a0001c0001t0019g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2042-11664C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652872 | ||||||
| chr15:55653061
|
T | C | 1 | a0002c0002t0015g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2042-11853A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653061 | ||||||
| chr15:55653183
|
T | A | 180 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(177): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.2042-11975A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653183 | ||||||
| chr15:55653255
|
A | G | 162 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(159): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2042-12047T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653255 | ||||||
| chr15:55653291
|
T | C | 12 | a0001c0001t0033g0098a0003c0004t0024g0056a0003c0004t0024g0057others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2042-12083A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653291 | ||||||
| chr15:55653412
|
C | A | 180 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(177): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.2042-12204G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653412 | ||||||
| chr15:55653463
|
AT | A | 43 | a0001c0001t0001g0156a0001c0001t0011g0075a0001c0001t0011g0091others(40): Show | 44 | HG00323.hp2 HG01081.hp1 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2042-12256delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653463 | ||||||
| chr15:55653620
|
A | T | 167 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(164): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2042-12412T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653620 | ||||||
| chr15:55653735
|
A | C | 8 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2042-12527T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653735 | ||||||
| chr15:55654070
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-12862G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654070 | ||||||
| chr15:55654100
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0089g0202 | 2 | HG02040.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2042-12892A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654100 | ||||||
| chr15:55654117
|
C | T | 2 | a0004c0006t0009g0015a0004c0006t0046g0012 | 2 | HG00733.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2042-12909G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654117 | ||||||
| chr15:55654184
|
C | A | 163 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(160): Show | 164 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2042-12976G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654184 | ||||||
| chr15:55654206
|
C | T | 5 | a0001c0001t0033g0103a0001c0001t0034g0101a0001c0001t0034g0102others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-12998G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654206 | ||||||
| chr15:55654262
|
G | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2042-13054C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654262 | ||||||
| chr15:55654268
|
A | C | 163 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(160): Show | 164 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2042-13060T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654268 | ||||||
| chr15:55654387
|
C | T | 90 | a0001c0001t0033g0098a0001c0001t0035g0001a0001c0001t0076g0133others(87): Show | 91 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2042-13179G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654387 | ||||||
| chr15:55654389
|
A | G | 162 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(159): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2042-13181T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654389 | ||||||
| chr15:55654420
|
C | T | 162 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(159): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2042-13212G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654420 | ||||||
| chr15:55654534
|
C | T | 56 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(53): Show | 56 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2042-13326G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654534 | ||||||
| chr15:55654810
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-13602G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654810 | ||||||
| chr15:55654817
|
G | A | 13 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.2042-13609C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654817 | ||||||
| chr15:55654830
|
G | A | 5 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0041g0135others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-13622C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654830 | ||||||
| chr15:55654918
|
T | C | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2042-13710A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654918 | ||||||
| chr15:55654984
|
C | T | 9 | a0002c0002t0013g0020a0002c0002t0013g0024a0002c0002t0013g0033others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2042-13776G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654984 | ||||||
| chr15:55655110
|
C | G | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-13902G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655110 | ||||||
| chr15:55655152
|
T | C | 2 | a0001c0007t0116g0109a0001c0007t0117g0110 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2042-13944A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655152 | ||||||
| chr15:55655168
|
T | C | 1 | a0002c0002t0021g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2042-13960A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655168 | ||||||
| chr15:55655352
|
A | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-14144T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655352 | ||||||
| chr15:55655354
|
G | A | 164 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(161): Show | 165 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2042-14146C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655354 | ||||||
| chr15:55655355
|
T | A | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-14147A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655355 | ||||||
| chr15:55655452
|
A | C | 2 | a0001c0001t0001g0134a0002c0002t0114g0215 | 2 | HG02683.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2042-14244T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655452 | ||||||
| chr15:55655463
|
T | A | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-14255A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655463 | ||||||
| chr15:55655475
|
T | C | 76 | a0001c0003t0003g0042a0001c0003t0003g0069a0001c0003t0003g0073others(73): Show | 76 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.2042-14267A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655475 | ||||||
| chr15:55655786
|
T | A | 3 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2042-14578A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655786 | ||||||
| chr15:55656240
|
A | G | 1 | a0002c0002t0066g0083 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2042-15032T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656240 | ||||||
| chr15:55656245
|
T | A | 1 | a0001c0001t0040g0166 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2042-15037A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656245 | ||||||
| chr15:55656321
|
G | A | 2 | a0003c0004t0031g0097a0003c0004t0031g0105 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2042-15113C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656321 | ||||||
| chr15:55656360
|
C | T | 1 | a0001c0003t0018g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2042-15152G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656360 | ||||||
| chr15:55656738
|
G | A | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2042-15530C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656738 | ||||||
| chr15:55656887
|
T | C | 3 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+15558A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656887 | ||||||
| chr15:55656937
|
G | A | 5 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0093g0125others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2041+15508C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656937 | ||||||
| chr15:55656942
|
C | T | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2041+15503G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656942 | ||||||
| chr15:55656946
|
C | T | 11 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0030g0092others(8): Show | 11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2041+15499G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656946 | ||||||
| chr15:55657041
|
T | C | 14 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(11): Show | 14 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2041+15404A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657041 | ||||||
| chr15:55657149
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2041+15296A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657149 | ||||||
| chr15:55657175
|
A | G | 1 | a0001c0001t0004g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2041+15270T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657175 | ||||||
| chr15:55657293
|
T | C | 1 | a0003c0004t0052g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2041+15152A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657293 | ||||||
| chr15:55657375
|
T | C | 3 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+15070A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657375 | ||||||
| chr15:55657477
|
A | C | 1 | a0001c0001t0002g0271 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2041+14968T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657477 | ||||||
| chr15:55657551
|
C | T | 178 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(175): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2041+14894G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657551 | ||||||
| chr15:55657778
|
T | C | 1 | a0002c0002t0073g0104 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2041+14667A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657778 | ||||||
| chr15:55657884
|
C | A | 45 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0023g0051others(42): Show | 46 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.2041+14561G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657884 | ||||||
| chr15:55657905
|
C | G | 1 | a0001c0001t0042g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2041+14540G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657905 | ||||||
| chr15:55657971
|
T | G | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+14474A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657971 | ||||||
| chr15:55658219
|
T | C | 3 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+14226A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658219 | ||||||
| chr15:55658313
|
T | A | 9 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0092g0127others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2041+14132A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658313 | ||||||
| chr15:55658319
|
T | A | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2041+14126A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658319 | ||||||
| chr15:55658320
|
T | A | 1 | a0001c0001t0011g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2041+14125A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658320 | ||||||
| chr15:55658322
|
T | A | 4 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228others(1): Show | 4 | HG02647.hp2 HG02976.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2041+14123A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658322 | ||||||
| chr15:55658441
|
G | A | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+14004C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658441 | ||||||
| chr15:55658511
|
C | T | 178 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(175): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2041+13934G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658511 | ||||||
| chr15:55658558
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+13887G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658558 | ||||||
| chr15:55658587
|
A | T | 5 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(2): Show | 5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+13858T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658587 | ||||||
| chr15:55658743
|
C | T | 162 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(159): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2041+13702G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658743 | ||||||
| chr15:55659044
|
T | C | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+13401A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659044 | ||||||
| chr15:55659234
|
A | G | 124 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(121): Show | 124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2041+13211T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659234 | ||||||
| chr15:55659317
|
A | G | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2041+13128T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659317 | ||||||
| chr15:55659327
|
G | C | 1 | a0001c0003t0005g0225 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2041+13118C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659327 | ||||||
| chr15:55659588
|
C | T | 16 | a0002c0002t0012g0018a0002c0002t0012g0028a0002c0002t0013g0020others(13): Show | 16 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.2041+12857G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659588 | ||||||
| chr15:55659867
|
C | T | 1 | a0001c0001t0107g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2041+12578G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659867 | ||||||
| chr15:55659927
|
A | AAAAAC | 20 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0030g0092others(17): Show | 21 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2041+12513_2041+12 others(11): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | ||||||
| chr15:55659927
|
A | AAAAACAA others(3): Show |
246 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2041+12508_2041+12 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | ||||||
| chr15:55659927
|
A | AAAAACAA others(8): Show |
9 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0245others(6): Show | 9 | HG00741.hp2 HG01106.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2041+12503_2041+12 others(21): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | ||||||
| chr15:55659927
|
A | AAAAACAA others(13): Show |
1 | a0001c0001t0002g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2041+12498_2041+12 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | ||||||
| chr15:55659927
|
A | AAAAACAA others(18): Show |
2 | a0001c0001t0033g0098a0011c0019t0051g0003 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2041+12493_2041+12 others(31): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | ||||||
| chr15:55660085
|
G | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+12360C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660085 | ||||||
| chr15:55660254
|
T | A | 14 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(11): Show | 14 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2041+12191A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660254 | ||||||
| chr15:55660431
|
T | C | 1 | a0001c0003t0005g0191 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2041+12014A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660431 | ||||||
| chr15:55660892
|
G | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+11553C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660892 | ||||||
| chr15:55661056
|
T | C | 3 | a0001c0001t0001g0196a0001c0001t0086g0197a0001c0001t0091g0190 | 3 | HG03098.hp1 HG03225.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2041+11389A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661056 | ||||||
| chr15:55661402
|
A | T | 77 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2041+11043T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661402 | ||||||
| chr15:55661509
|
C | CTTTA | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+10932_2041+10 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661509 | ||||||
| chr15:55661810
|
C | T | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+10635G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661810 | ||||||
| chr15:55661821
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2041+10624G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661821 | ||||||
| chr15:55661895
|
TA | T | 167 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(164): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2041+10549delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661895 | ||||||
| chr15:55661895
|
TAA | T | 10 | a0001c0001t0002g0277a0002c0002t0013g0020a0002c0002t0013g0024others(7): Show | 10 | HG01167.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2041+10548_2041+10 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661895 | ||||||
| chr15:55661920
|
T | A | 11 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0030g0092others(8): Show | 11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2041+10525A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661920 | ||||||
| chr15:55661965
|
T | G | 6 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(3): Show | 6 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2041+10480A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661965 | ||||||
| chr15:55662004
|
A | G | 3 | a0001c0001t0023g0051a0001c0001t0023g0058a0011c0019t0051g0003 | 3 | HG02809.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2041+10441T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662004 | ||||||
| chr15:55662009
|
G | T | 2 | a0002c0002t0027g0023a0002c0002t0028g0022 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2041+10436C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662009 | ||||||
| chr15:55662211
|
T | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+10234A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662211 | ||||||
| chr15:55662280
|
T | C | 1 | a0002c0002t0005g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2041+10165A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662280 | ||||||
| chr15:55662309
|
T | C | 14 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(11): Show | 14 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2041+10136A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662309 | ||||||
| chr15:55662385
|
A | T | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+10060T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662385 | ||||||
| chr15:55662498
|
C | G | 15 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.2041+9947G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662498 | ||||||
| chr15:55662807
|
A | G | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2041+9638T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662807 | ||||||
| chr15:55662906
|
C | T | 6 | a0002c0002t0010g0048a0002c0002t0010g0049a0002c0002t0010g0050others(3): Show | 6 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+9539G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662906 | ||||||
| chr15:55662907
|
G | A | 6 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0185others(3): Show | 6 | HG00140.hp2 HG00639.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+9538C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662907 | ||||||
| chr15:55663073
|
C | T | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+9372G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663073 | ||||||
| chr15:55663254
|
A | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+9191T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663254 | ||||||
| chr15:55663539
|
C | CT | 9 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(6): Show | 9 | HG02630.hp2 HG02970.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.2041+8905dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663539 | ||||||
| chr15:55663539
|
C | T | 2 | a0001c0001t0004g0243a0001c0001t0004g0244 | 2 | HG00639.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2041+8906G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663539 | ||||||
| chr15:55663591
|
G | A | 2 | a0002c0002t0074g0099a0002c0002t0120g0236 | 2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2041+8854C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663591 | ||||||
| chr15:55663666
|
G | C | 188 | a0001c0001t0001g0183a0001c0001t0001g0226a0001c0001t0002g0238others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2041+8779C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663666 | ||||||
| chr15:55663692
|
C | A | 4 | a0002c0002t0003g0076a0005c0010t0026g0065a0005c0010t0064g0072others(1): Show | 4 | NA18944.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2041+8753G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663692 | ||||||
| chr15:55663774
|
T | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+8671A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663774 | ||||||
| chr15:55663807
|
G | A | 12 | a0001c0001t0033g0098a0003c0004t0024g0056a0003c0004t0024g0057others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2041+8638C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663807 | ||||||
| chr15:55663944
|
C | T | 10 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(7): Show | 10 | HG02615.hp1 HG02630.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2041+8501G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663944 | ||||||
| chr15:55664017
|
C | T | 10 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(7): Show | 10 | HG02615.hp1 HG02630.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2041+8428G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664017 | ||||||
| chr15:55664145
|
T | C | 1 | a0001c0001t0085g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2041+8300A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664145 | ||||||
| chr15:55664186
|
G | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0165 | 3 | NA18962.hp1 NA18981.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2041+8259C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664186 | ||||||
| chr15:55664228
|
G | GC | 8 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+8216dupG | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664228 | ||||||
| chr15:55664360
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2041+8085G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664360 | ||||||
| chr15:55664368
|
C | T | 1 | a0001c0007t0039g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2041+8077G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664368 | ||||||
| chr15:55664423
|
G | A | 4 | a0001c0001t0001g0226a0001c0001t0004g0281a0001c0001t0004g0282others(1): Show | 4 | HG01361.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2041+8022C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664423 | ||||||
| chr15:55664567
|
A | C | 3 | a0002c0002t0020g0052a0002c0002t0020g0060a0002c0002t0021g0010 | 3 | HG02451.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2041+7878T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664567 | ||||||
| chr15:55664672
|
G | A | 249 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(246): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2041+7773C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664672 | ||||||
| chr15:55664715
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2041+7730A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664715 | ||||||
| chr15:55664769
|
T | C | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2041+7676A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664769 | ||||||
| chr15:55664842
|
C | G | 1 | a0001c0001t0042g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2041+7603G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664842 | ||||||
| chr15:55664847
|
T | A | 252 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(249): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.2041+7598A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664847 | ||||||
| chr15:55664926
|
T | C | 8 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+7519A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664926 | ||||||
| chr15:55664997
|
G | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+7448C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664997 | ||||||
| chr15:55665029
|
C | T | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2041+7416G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665029 | ||||||
| chr15:55665191
|
T | A | 1 | a0002c0002t0007g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2041+7254A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665191 | ||||||
| chr15:55665455
|
G | C | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2041+6990C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665455 | ||||||
| chr15:55665506
|
TG | T | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+6938delC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665506 | ||||||
| chr15:55665507
|
G | GT | 8 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+6937dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665507 | ||||||
| chr15:55665507
|
G | T | 4 | a0001c0012t0078g0113a0001c0012t0080g0114a0002c0002t0074g0099others(1): Show | 4 | HG02630.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2041+6938C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665507 | ||||||
| chr15:55665507
|
GT | G | 52 | a0001c0001t0001g0130a0001c0001t0001g0226a0001c0001t0002g0238others(49): Show | 52 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2041+6937delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665507 | ||||||
| chr15:55665516
|
T | C | 2 | a0001c0001t0006g0163a0001c0001t0119g0160 | 2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2041+6929A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665516 | ||||||
| chr15:55665909
|
A | G | 1 | a0001c0009t0049g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2041+6536T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665909 | ||||||
| chr15:55666219
|
T | C | 144 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.2041+6226A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666219 | ||||||
| chr15:55666266
|
C | T | 22 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0106g0229others(19): Show | 22 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2041+6179G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666266 | ||||||
| chr15:55666531
|
T | G | 4 | a0001c0001t0001g0226a0001c0001t0004g0281a0001c0001t0004g0282others(1): Show | 4 | HG01361.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2041+5914A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666531 | ||||||
| chr15:55666592
|
A | G | 2 | a0002c0002t0005g0108a0002c0002t0005g0216 | 2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2041+5853T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666592 | ||||||
| chr15:55666619
|
C | T | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2041+5826G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666619 | ||||||
| chr15:55667158
|
A | G | 2 | a0001c0001t0041g0135a0001c0001t0041g0136 | 2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2041+5287T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667158 | ||||||
| chr15:55667193
|
G | A | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2041+5252C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667193 | ||||||
| chr15:55667206
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2041+5239T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667206 | ||||||
| chr15:55667207
|
GA | G | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(105): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2041+5237delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667207 | ||||||
| chr15:55667207
|
GAA | G | 20 | a0001c0001t0001g0188a0001c0001t0001g0195a0001c0001t0023g0051others(17): Show | 20 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2041+5236_2041+523 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667207 | ||||||
| chr15:55667220
|
A | C | 144 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.2041+5225T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667220 | ||||||
| chr15:55667262
|
T | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+5183A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667262 | ||||||
| chr15:55667431
|
A | T | 5 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(2): Show | 5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+5014T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667431 | ||||||
| chr15:55667457
|
G | A | 1 | a0001c0001t0042g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2041+4988C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667457 | ||||||
| chr15:55667553
|
G | A | 1 | a0001c0003t0003g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2041+4892C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667553 | ||||||
| chr15:55667762
|
A | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+4683T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667762 | ||||||
| chr15:55667834
|
C | T | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2041+4611G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667834 | ||||||
| chr15:55667912
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2041+4533G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667912 | ||||||
| chr15:55667967
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2041+4478C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667967 | ||||||
| chr15:55668001
|
G | A | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2041+4444C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668001 | ||||||
| chr15:55668077
|
T | A | 1 | a0001c0001t0004g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2041+4368A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668077 | ||||||
| chr15:55668258
|
A | G | 78 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.2041+4187T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668258 | ||||||
| chr15:55668491
|
G | C | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+3954C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668491 | ||||||
| chr15:55669174
|
A | T | 33 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0106g0229others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.2041+3271T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55669174 | ||||||
| chr15:55669297
|
C | T | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+3148G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55669297 | ||||||
| chr15:55669368
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2041+3077T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55669368 | ||||||
| chr15:55670019
|
A | C | 3 | a0001c0012t0078g0113a0001c0012t0080g0114a0011c0019t0051g0003 | 3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2041+2426T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670019 | ||||||
| chr15:55670101
|
T | C | 18 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0007t0039g0230others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.2041+2344A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670101 | ||||||
| chr15:55670159
|
C | T | 263 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2041+2286G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670159 | ||||||
| chr15:55670182
|
T | G | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2041+2263A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670182 | ||||||
| chr15:55670247
|
G | GT | 266 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2041+2197dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670247 | ||||||
| chr15:55670326
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2041+2119C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670326 | ||||||
| chr15:55670490
|
G | A | 1 | a0001c0001t0087g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2041+1955C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670490 | ||||||
| chr15:55670578
|
C | T | 263 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2041+1867G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670578 | ||||||
| chr15:55670663
|
G | A | 87 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.2041+1782C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670663 | ||||||
| chr15:55670840
|
C | T | 1 | a0001c0001t0008g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2041+1605G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670840 | ||||||
| chr15:55670895
|
C | T | 1 | a0001c0001t0076g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2041+1550G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670895 | ||||||
| chr15:55670897
|
TCACAAAC others(5): Show |
T | 1 | a0001c0001t0036g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2041+1536_2041+154 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670897 | ||||||
| chr15:55670901
|
AAACACAC others(6): Show |
A | 1 | a0001c0001t0002g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2041+1531_2041+154 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | ||||||
| chr15:55670901
|
AAACACAC others(8): Show |
A | 1 | a0002c0002t0062g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2041+1529_2041+154 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | ||||||
| chr15:55670901
|
AAACACAC others(10): Show |
A | 1 | a0001c0001t0019g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2041+1527_2041+154 others(21): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | ||||||
| chr15:55670901
|
AAACACAC others(12): Show |
A | 2 | a0001c0001t0014g0154a0001c0001t0040g0166 | 2 | NA18952.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2041+1525_2041+154 others(23): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | ||||||
| chr15:55670902
|
AACAC | A | 7 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0072g0094others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2041+1539_2041+154 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(3): Show |
A | 8 | a0001c0001t0034g0101a0001c0001t0059g0005a0001c0001t0107g0221others(5): Show | 8 | HG02572.hp2 HG02818.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+1533_2041+154 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(5): Show |
A | 11 | a0001c0001t0004g0255a0001c0001t0004g0258a0001c0001t0033g0103others(8): Show | 11 | HG01517.hp1 HG02965.hp1 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.2041+1531_2041+154 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(7): Show |
A | 105 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(102): Show | 105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.2041+1529_2041+154 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(9): Show |
A | 16 | a0001c0001t0002g0245a0001c0001t0004g0250a0001c0001t0087g0148others(13): Show | 16 | HG01358.hp1 HG02040.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2041+1527_2041+154 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(11): Show |
A | 14 | a0001c0001t0001g0182a0001c0001t0008g0223a0001c0001t0014g0167others(11): Show | 14 | HG00280.hp1 HG01361.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2041+1525_2041+154 others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(13): Show |
A | 76 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(73): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2041+1523_2041+154 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(15): Show |
A | 13 | a0001c0001t0001g0155a0001c0001t0001g0177a0001c0001t0008g0207others(10): Show | 13 | HG00099.hp1 HG01358.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2041+1521_2041+154 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(17): Show |
A | 10 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(7): Show | 10 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2041+1519_2041+154 others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(19): Show |
A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+1517_2041+154 others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670902
|
AACACACA others(21): Show |
A | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2041+1515_2041+154 others(32): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | ||||||
| chr15:55670953
|
A | T | 1 | a0001c0001t0115g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2041+1492T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670953 | ||||||
| chr15:55670971
|
AAGAAG | A | 3 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+1469_2041+147 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670971 | ||||||
| chr15:55671037
|
T | A | 1 | a0003c0004t0053g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2041+1408A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671037 | ||||||
| chr15:55671204
|
A | G | 264 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2041+1241T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671204 | ||||||
| chr15:55671534
|
G | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+911C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671534 | ||||||
| chr15:55671549
|
T | C | 3 | a0002c0002t0020g0052a0002c0002t0020g0060a0002c0002t0021g0010 | 3 | HG02451.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2041+896A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671549 | ||||||
| chr15:55671566
|
T | C | 5 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0041g0135others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.2041+879A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671566 | ||||||
| chr15:55671574
|
C | T | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2041+871G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671574 | ||||||
| chr15:55671588
|
A | T | 266 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2041+857T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671588 | ||||||
| chr15:55671642
|
G | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+803C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671642 | ||||||
| chr15:55671646
|
G | A | 44 | a0001c0001t0001g0226a0001c0001t0002g0240a0001c0001t0002g0241others(41): Show | 44 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2041+799C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671646 | ||||||
| chr15:55671747
|
C | T | 17 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(14): Show | 18 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2041+698G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671747 | ||||||
| chr15:55671755
|
C | T | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2041+690G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671755 | ||||||
| chr15:55671970
|
G | A | 1 | a0002c0002t0007g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2041+475C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671970 | ||||||
| chr15:55672134
|
C | T | 2 | a0004c0006t0009g0007a0004c0006t0009g0008 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2041+311G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55672134 | ||||||
| chr15:55672143
|
CT | C | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+301delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55672143 | ||||||
| chr15:55672355
|
G | C | 15 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(12): Show | 15 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2041+90C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55672355 | ||||||
| chr15:55672782
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1853-149T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55672782 | ||||||
| chr15:55673040
|
C | CTGAA | 3 | a0001c0012t0078g0113a0001c0012t0080g0114a0011c0019t0051g0003 | 3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1852+327_1852+330d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673040 | ||||||
| chr15:55673259
|
G | T | 1 | a0002c0002t0005g0216 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1852+112C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673259 | ||||||
| chr15:55673292
|
TATAAAC | T | 13 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1852+73_1852+78del others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673292 | ||||||
| chr15:55673323
|
T | C | 89 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1852+48A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673323 | ||||||
| chr15:55673336
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1852+35T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673336 | ||||||
| chr15:55673344
|
T | A | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1852+27A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673344 | ||||||
| chr15:55673773
|
T | C | 78 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1547-97A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55673773 | ||||||
| chr15:55673911
|
T | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1547-235A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55673911 | ||||||
| chr15:55674043
|
T | G | 189 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1547-367A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674043 | ||||||
| chr15:55674119
|
A | G | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1547-443T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674119 | ||||||
| chr15:55674247
|
G | C | 11 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0030g0092others(8): Show | 11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1547-571C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674247 | ||||||
| chr15:55674416
|
T | C | 2 | a0001c0009t0113g0233a0010c0014t0079g0234 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1547-740A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674416 | ||||||
| chr15:55674444
|
C | A | 134 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0023g0051others(131): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1547-768G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674444 | ||||||
| chr15:55674499
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1547-823A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674499 | ||||||
| chr15:55674782
|
G | A | 12 | a0001c0001t0033g0098a0003c0004t0024g0056a0003c0004t0024g0057others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546+737C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674782 | ||||||
| chr15:55674820
|
C | T | 282 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1546+699G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674820 | ||||||
| chr15:55675199
|
A | G | 44 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0023g0051others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1546+320T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55675199 | ||||||
| chr15:55675718
|
T | C | 92 | a0001c0001t0033g0098a0001c0003t0003g0042a0001c0003t0003g0069others(89): Show | 92 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1382-35A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675718 | ||||||
| chr15:55675752
|
C | A | 1 | a0002c0002t0105g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1382-69G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675752 | ||||||
| chr15:55675777
|
C | G | 17 | a0002c0002t0012g0016a0002c0002t0012g0018a0002c0002t0012g0028others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1382-94G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675777 | ||||||
| chr15:55675784
|
C | A | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1382-101G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675784 | ||||||
| chr15:55676272
|
GT | G | 90 | a0001c0001t0033g0098a0001c0003t0003g0042a0001c0003t0003g0069others(87): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1382-590delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676272 | ||||||
| chr15:55676278
|
T | C | 1 | a0001c0001t0006g0162 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1382-595A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676278 | ||||||
| chr15:55676341
|
G | A | 82 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1382-658C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676341 | ||||||
| chr15:55676401
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1382-718A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676401 | ||||||
| chr15:55676527
|
A | G | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1382-844T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676527 | ||||||
| chr15:55676657
|
C | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1382-974G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676657 | ||||||
| chr15:55676726
|
G | T | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1382-1043C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676726 | ||||||
| chr15:55676919
|
A | G | 1 | a0001c0001t0094g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1381+878T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676919 | ||||||
| chr15:55677013
|
C | T | 2 | a0001c0001t0004g0259a0001c0001t0004g0263 | 2 | HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1381+784G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677013 | ||||||
| chr15:55677046
|
T | C | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1381+751A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677046 | ||||||
| chr15:55677380
|
C | T | 1 | a0001c0007t0039g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1381+417G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677380 | ||||||
| chr15:55677569
|
T | C | 4 | a0002c0002t0012g0018a0002c0002t0029g0019a0002c0002t0067g0027others(1): Show | 4 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+228A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677569 | ||||||
| chr15:55677572
|
T | C | 4 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(1): Show | 4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+225A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677572 | ||||||
| chr15:55677629
|
A | C | 1 | a0001c0001t0077g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1381+168T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677629 | ||||||
| chr15:55678091
|
A | G | 1 | a0001c0007t0039g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1134-47T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678091 | ||||||
| chr15:55678121
|
A | G | 1 | a0011c0019t0051g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1134-77T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678121 | ||||||
| chr15:55678210
|
T | C | 2 | a0001c0001t0056g0004a0001c0001t0057g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1134-166A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678210 | ||||||
| chr15:55678386
|
A | C | 1 | a0002c0002t0020g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1134-342T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678386 | ||||||
| chr15:55678395
|
A | T | 6 | a0002c0002t0012g0018a0002c0002t0012g0028a0002c0002t0029g0019others(3): Show | 6 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134-351T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678395 | ||||||
| chr15:55678725
|
T | C | 1 | a0002c0002t0026g0078 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1133+561A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678725 | ||||||
| chr15:55678852
|
T | C | 1 | a0002c0002t0062g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1133+434A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678852 | ||||||
| chr15:55678854
|
G | T | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1133+432C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678854 | ||||||
| chr15:55679031
|
G | A | 1 | a0002c0002t0074g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1133+255C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55679031 | ||||||
| chr15:55679187
|
A | T | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+99T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55679187 | ||||||
| chr15:55679458
|
A | G | 1 | a0002c0002t0062g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.974-13T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679458 | ||||||
| chr15:55679487
|
T | C | 2 | a0001c0001t0056g0004a0001c0001t0057g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.974-42A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679487 | ||||||
| chr15:55679539
|
T | C | 15 | a0001c0001t0023g0051a0001c0001t0023g0058a0004c0005t0022g0039others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.974-94A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679539 | ||||||
| chr15:55679986
|
A | G | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+68T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679986 | ||||||
| chr15:55679988
|
G | A | 1 | a0002c0002t0120g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.973+66C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679988 | ||||||
| chr15:55680011
|
T | C | 1 | a0001c0001t0106g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.973+43A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55680011 | ||||||
| chr15:55680245
|
T | C | 5 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0256others(2): Show | 5 | HG03834.hp2 NA18962.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-33A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/19 | chr15 | 55680245 | ||||||
| chr15:55680317
|
A | G | 274 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.815-105T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/19 | chr15 | 55680317 | ||||||
| chr15:55680453
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0042g0280 | 2 | HG01361.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.814+38T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/19 | chr15 | 55680453 | ||||||
| chr15:55680646
|
C | G | 1 | a0005c0010t0026g0065 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.677-18G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55680646 | ||||||
| chr15:55680675
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.677-47A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55680675 | ||||||
| chr15:55680940
|
T | G | 53 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(50): Show | 53 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.677-312A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55680940 | ||||||
| chr15:55681031
|
A | C | 3 | a0001c0001t0023g0051a0001c0001t0023g0058a0011c0019t0051g0003 | 3 | HG02809.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.677-403T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681031 | ||||||
| chr15:55681200
|
A | T | 7 | a0001c0001t0033g0103a0001c0001t0034g0101a0001c0001t0034g0102others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.677-572T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681200 | ||||||
| chr15:55681318
|
C | T | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.677-690G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681318 | ||||||
| chr15:55681548
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.676+816C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681548 | ||||||
| chr15:55681572
|
T | C | 5 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0041g0135others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+792A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681572 | ||||||
| chr15:55681776
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.676+588C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681776 | ||||||
| chr15:55681847
|
G | A | 1 | a0002c0002t0069g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.676+517C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681847 | ||||||
| chr15:55682111
|
G | A | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+253C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682111 | ||||||
| chr15:55682121
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.676+243G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682121 | ||||||
| chr15:55682186
|
T | C | 11 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0030g0092others(8): Show | 11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+178A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682186 | ||||||
| chr15:55682228
|
A | C | 2 | a0002c0002t0114g0215a0002c0002t0121g0237 | 2 | HG01074.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.676+136T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682228 | ||||||
| chr15:55682297
|
G | A | 2 | a0002c0002t0005g0108a0002c0002t0005g0216 | 2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.676+67C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682297 | ||||||
| chr15:55682330
|
G | A | 1 | a0001c0001t0011g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.676+34C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682330 | ||||||
| chr15:55682348
|
C | T | 3 | a0001c0007t0116g0109a0001c0007t0117g0110a0001c0007t0118g0111 | 3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.676+16G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682348 | ||||||
| chr15:55682357
|
G | A | 2 | a0001c0001t0036g0218a0001c0001t0110g0217 | 2 | HG02257.hp2 HG02572.hp1 |
splice_region_variant&intron_variant | LOW | c.676+7C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682357 | ||||||
| chr15:55682543
|
A | ATTTT | 4 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0084g0192others(1): Show | 4 | HG04228.hp1 NA18973.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-50_543-47dupAA others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682543 | ||||||
| chr15:55682544
|
T | TTTTA | 27 | a0001c0001t0023g0051a0001c0001t0023g0058a0001c0001t0025g0013others(24): Show | 28 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.543-51_543-48dupTA others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682544
|
T | TTTTATTT others(1): Show |
36 | a0001c0001t0002g0246a0001c0001t0002g0265a0001c0001t0002g0266others(33): Show | 36 | HG00323.hp1 HG01081.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.543-55_543-48dupTA others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682544
|
T | TTTTATTT others(5): Show |
63 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(60): Show | 63 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.543-59_543-48dupTA others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682544
|
T | TTTTATTT others(9): Show |
28 | a0001c0001t0002g0273a0001c0001t0004g0264a0001c0001t0043g0272others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.543-63_543-48dupTA others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682544
|
T | TTTTATTT others(13): Show |
3 | a0001c0001t0106g0229a0001c0007t0116g0109a0001c0007t0117g0110 | 3 | HG02109.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.543-67_543-48dupTA others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682544
|
T | TTTTTTTT others(5): Show |
1 | a0001c0007t0039g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.543-48_543-47insTA others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682544
|
T | TTTTTTTT others(13): Show |
2 | a0001c0007t0039g0231a0001c0007t0118g0111 | 2 | HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.543-48_543-47insTA others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682544
|
TTTTATTT others(5): Show |
T | 12 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0030g0092others(9): Show | 12 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.543-59_543-48delTA others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | ||||||
| chr15:55682548
|
A | T | 69 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.543-51T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682548 | ||||||
| chr15:55682553
|
T | TTTATTTA others(9): Show |
7 | a0002c0002t0003g0043a0002c0002t0003g0087a0002c0002t0003g0088others(4): Show | 7 | HG00438.hp2 HG02027.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-57_543-56insTT others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682553 | ||||||
| chr15:55682560
|
A | T | 1 | a0001c0001t0115g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.543-63T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682560 | ||||||
| chr15:55682676
|
C | T | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.543-179G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682676 | ||||||
| chr15:55682756
|
T | C | 53 | a0001c0001t0001g0226a0001c0001t0002g0238a0001c0001t0002g0240others(50): Show | 53 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.543-259A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682756 | ||||||
| chr15:55682796
|
C | G | 1 | a0002c0002t0003g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.543-299G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682796 | ||||||
| chr15:55682887
|
A | G | 80 | a0001c0003t0003g0042a0001c0003t0003g0069a0001c0003t0003g0073others(77): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.543-390T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682887 | ||||||
| chr15:55683056
|
C | T | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-559G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683056 | ||||||
| chr15:55683185
|
C | CT | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.542+601dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683185 | ||||||
| chr15:55683294
|
T | C | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.542+493A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683294 | ||||||
| chr15:55683402
|
T | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.542+385A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683402 | ||||||
| chr15:55683748
|
A | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.542+39T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683748 | ||||||
| chr15:55684132
|
C | T | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-201G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684132 | ||||||
| chr15:55684510
|
C | T | 11 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(8): Show | 11 | HG02615.hp1 HG02630.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.398-579G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684510 | ||||||
| chr15:55684628
|
T | G | 1 | a0001c0001t0107g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.398-697A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684628 | ||||||
| chr15:55684704
|
T | TG | 267 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.398-774dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684704 | ||||||
| chr15:55684762
|
C | T | 19 | a0001c0001t0001g0224a0001c0001t0023g0051a0001c0001t0023g0058others(16): Show | 19 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.398-831G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684762 | ||||||
| chr15:55684820
|
A | C | 6 | a0001c0001t0030g0092a0001c0001t0056g0004a0001c0001t0057g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-889T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684820 | ||||||
| chr15:55684861
|
T | C | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-930A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684861 | ||||||
| chr15:55685102
|
C | T | 79 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.398-1171G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685102 | ||||||
| chr15:55685382
|
A | G | 7 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-1451T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685382 | ||||||
| chr15:55685544
|
G | C | 2 | a0001c0001t0023g0051a0001c0001t0023g0058 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.398-1613C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685544 | ||||||
| chr15:55685569
|
C | A | 5 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-1638G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685569 | ||||||
| chr15:55685673
|
A | T | 5 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(2): Show | 5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-1742T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685673 | ||||||
| chr15:55685826
|
G | C | 87 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.398-1895C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685826 | ||||||
| chr15:55685992
|
T | C | 1 | a0002c0002t0105g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.398-2061A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685992 | ||||||
| chr15:55686243
|
T | A | 88 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.398-2312A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686243 | ||||||
| chr15:55686348
|
T | C | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-2417A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686348 | ||||||
| chr15:55686469
|
A | G | 1 | a0001c0001t0004g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.398-2538T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686469 | ||||||
| chr15:55686612
|
T | C | 7 | a0001c0001t0036g0218a0001c0001t0110g0217a0001c0007t0039g0230others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-2681A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686612 | ||||||
| chr15:55686776
|
C | T | 1 | a0001c0001t0036g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.398-2845G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686776 | ||||||
| chr15:55686932
|
C | T | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-3001G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686932 | ||||||
| chr15:55687006
|
C | T | 8 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(5): Show | 8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-3075G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55687006 | ||||||
| chr15:55687802
|
T | C | 1 | a0002c0002t0121g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.398-3871A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55687802 | ||||||
| chr15:55687851
|
G | A | 1 | a0001c0001t0023g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.398-3920C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55687851 | ||||||
| chr15:55688100
|
G | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-4169C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688100 | ||||||
| chr15:55688401
|
T | TTA | 99 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.398-4472_398-4471d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688401 | ||||||
| chr15:55688493
|
C | T | 1 | a0001c0012t0080g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.398-4562G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688493 | ||||||
| chr15:55688670
|
C | G | 1 | a0005c0010t0064g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.398-4739G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688670 | ||||||
| chr15:55688869
|
G | A | 1 | a0005c0010t0064g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.398-4938C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688869 | ||||||
| chr15:55689027
|
G | A | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-5096C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689027 | ||||||
| chr15:55689408
|
T | C | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-5477A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689408 | ||||||
| chr15:55689446
|
C | G | 1 | a0001c0001t0042g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.398-5515G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689446 | ||||||
| chr15:55689507
|
G | A | 1 | a0002c0002t0026g0078 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.398-5576C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689507 | ||||||
| chr15:55689603
|
G | A | 5 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0041g0135others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-5672C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689603 | ||||||
| chr15:55689632
|
T | TA | 267 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.398-5702dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689632 | ||||||
| chr15:55689743
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.398-5812G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689743 | ||||||
| chr15:55690014
|
A | G | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398-6083T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690014 | ||||||
| chr15:55690028
|
T | C | 2 | a0006c0011t0036g0220a0006c0011t0108g0222 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.398-6097A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690028 | ||||||
| chr15:55690059
|
T | C | 72 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0003t0018g0081others(69): Show | 72 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.398-6128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690059 | ||||||
| chr15:55690102
|
T | C | 6 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-6171A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690102 | ||||||
| chr15:55690321
|
T | C | 2 | a0001c0001t0056g0004a0001c0001t0057g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.398-6390A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690321 | ||||||
| chr15:55690373
|
C | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-6442G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690373 | ||||||
| chr15:55690622
|
C | T | 4 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(1): Show | 4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-6691G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690622 | ||||||
| chr15:55690643
|
T | C | 2 | a0002c0002t0114g0215a0002c0002t0121g0237 | 2 | HG01074.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.398-6712A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690643 | ||||||
| chr15:55690708
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.398-6777A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690708 | ||||||
| chr15:55690779
|
G | C | 252 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(249): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.398-6848C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690779 | ||||||
| chr15:55691071
|
G | C | 4 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(1): Show | 4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-7140C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691071 | ||||||
| chr15:55691073
|
T | C | 95 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.398-7142A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691073 | ||||||
| chr15:55691111
|
G | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-7180C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691111 | ||||||
| chr15:55691147
|
T | G | 4 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0093g0125others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-7216A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691147 | ||||||
| chr15:55691177
|
T | C | 2 | a0001c0001t0002g0241a0001c0001t0002g0245 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.398-7246A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691177 | ||||||
| chr15:55691296
|
CA | C | 43 | a0001c0001t0001g0161a0001c0001t0001g0176a0001c0001t0001g0179others(40): Show | 44 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-7366delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691296 | ||||||
| chr15:55691296
|
CAA | C | 44 | a0001c0001t0023g0051a0001c0001t0023g0058a0002c0002t0003g0009others(41): Show | 44 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-7367_398-7366d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691296 | ||||||
| chr15:55691296
|
CAAAAAAA | C | 7 | a0001c0001t0036g0218a0001c0001t0107g0221a0001c0001t0110g0217others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-7372_398-7366d others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691296 | ||||||
| chr15:55691315
|
A | AG | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-7385dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691315 | ||||||
| chr15:55691315
|
A | G | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-7384T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691315 | ||||||
| chr15:55691393
|
T | C | 4 | a0001c0001t0004g0259a0001c0001t0004g0263a0001c0001t0004g0264others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-7462A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691393 | ||||||
| chr15:55691509
|
T | C | 1 | a0001c0001t0008g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.398-7578A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691509 | ||||||
| chr15:55691515
|
C | T | 271 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.398-7584G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691515 | ||||||
| chr15:55691549
|
C | T | 1 | a0001c0001t0076g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.398-7618G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691549 | ||||||
| chr15:55691589
|
A | G | 56 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0001t0002g0238others(53): Show | 56 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.398-7658T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691589 | ||||||
| chr15:55691636
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.398-7705C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691636 | ||||||
| chr15:55691674
|
C | A | 1 | a0014c0018t0015g0189 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.398-7743G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691674 | ||||||
| chr15:55691680
|
C | CA | 13 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.398-7750dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691680 | ||||||
| chr15:55691732
|
A | G | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-7801T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691732 | ||||||
| chr15:55692067
|
T | C | 80 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(77): Show | 80 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.398-8136A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692067 | ||||||
| chr15:55692097
|
C | T | 1 | a0001c0009t0097g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.398-8166G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692097 | ||||||
| chr15:55692241
|
A | C | 47 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.398-8310T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692241 | ||||||
| chr15:55692334
|
G | A | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-8403C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692334 | ||||||
| chr15:55692407
|
A | C | 109 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.398-8476T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692407 | ||||||
| chr15:55692461
|
C | T | 151 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.398-8530G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692461 | ||||||
| chr15:55692663
|
T | G | 1 | a0004c0006t0009g0015 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.398-8732A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692663 | ||||||
| chr15:55692828
|
G | A | 1 | a0012c0017t0002g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.398-8897C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692828 | ||||||
| chr15:55692835
|
C | CT | 163 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.398-8905dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692835 | ||||||
| chr15:55692835
|
C | CTT | 10 | a0001c0001t0001g0188a0001c0001t0002g0261a0001c0001t0004g0256others(7): Show | 11 | HG02040.hp1 HG02630.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-8906_398-8905d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692835 | ||||||
| chr15:55692835
|
CT | C | 15 | a0001c0001t0011g0091a0001c0001t0034g0102a0002c0002t0017g0126others(12): Show | 15 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.398-8905delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692835 | ||||||
| chr15:55692904
|
G | A | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.398-8973C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692904 | ||||||
| chr15:55692934
|
G | A | 3 | a0001c0001t0035g0001a0001c0001t0040g0132a0001c0001t0076g0133 | 4 | HG03491.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-9003C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692934 | ||||||
| chr15:55693008
|
T | G | 51 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.398-9077A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693008 | ||||||
| chr15:55693241
|
G | C | 1 | a0001c0001t0040g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398-9310C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693241 | ||||||
| chr15:55693303
|
G | A | 54 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.398-9372C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693303 | ||||||
| chr15:55693322
|
G | A | 2 | a0001c0001t0042g0262a0002c0002t0003g0071 | 2 | HG00738.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.398-9391C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693322 | ||||||
| chr15:55693351
|
G | C | 55 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.398-9420C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693351 | ||||||
| chr15:55693360
|
GCAGGAGA others(5): Show |
G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-9441_398-9430d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693360 | ||||||
| chr15:55693373
|
T | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-9442A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693373 | ||||||
| chr15:55693603
|
T | C | 27 | a0001c0001t0025g0013a0001c0001t0025g0030a0002c0002t0010g0048others(24): Show | 27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.398-9672A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693603 | ||||||
| chr15:55694191
|
T | C | 2 | a0006c0011t0036g0220a0006c0011t0108g0222 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.398-10260A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694191 | ||||||
| chr15:55694254
|
G | C | 1 | a0002c0002t0120g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.398-10323C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694254 | ||||||
| chr15:55694582
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.398-10651A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694582 | ||||||
| chr15:55694869
|
C | A | 1 | a0001c0001t0087g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.398-10938G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694869 | ||||||
| chr15:55694987
|
C | T | 4 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0258others(1): Show | 4 | HG03834.hp2 NA18962.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-11056G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694987 | ||||||
| chr15:55695300
|
A | G | 47 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.398-11369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695300 | ||||||
| chr15:55695405
|
C | T | 1 | a0002c0002t0003g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.398-11474G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695405 | ||||||
| chr15:55695718
|
C | A | 31 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(28): Show | 31 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-11787G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695718 | ||||||
| chr15:55695744
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.398-11813G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695744 | ||||||
| chr15:55695859
|
T | C | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-11928A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695859 | ||||||
| chr15:55696184
|
A | G | 45 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(42): Show | 45 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.398-12253T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696184 | ||||||
| chr15:55696276
|
G | A | 1 | a0002c0002t0100g0214 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.398-12345C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696276 | ||||||
| chr15:55696340
|
A | G | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-12409T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696340 | ||||||
| chr15:55696392
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.398-12461C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696392 | ||||||
| chr15:55696438
|
T | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-12507A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696438 | ||||||
| chr15:55696617
|
C | T | 1 | a0001c0001t0040g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398-12686G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696617 | ||||||
| chr15:55696738
|
T | C | 2 | a0001c0001t0037g0169a0001c0001t0037g0172 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.398-12807A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696738 | ||||||
| chr15:55696861
|
T | C | 14 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-12930A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696861 | ||||||
| chr15:55696882
|
G | A | 148 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.398-12951C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696882 | ||||||
| chr15:55696905
|
T | A | 1 | a0002c0002t0121g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.398-12974A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696905 | ||||||
| chr15:55697039
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0182 | 2 | NA18954.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.398-13108C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697039 | ||||||
| chr15:55697329
|
G | C | 2 | a0001c0001t0008g0152a0001c0001t0008g0153 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.398-13398C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697329 | ||||||
| chr15:55697512
|
CTGTT | C | 7 | a0001c0001t0033g0098a0002c0002t0074g0099a0003c0004t0031g0097others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-13585_398-1358 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697512 | ||||||
| chr15:55697543
|
G | A | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.398-13612C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697543 | ||||||
| chr15:55697594
|
C | T | 32 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(29): Show | 32 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.398-13663G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697594 | ||||||
| chr15:55697741
|
C | T | 47 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.398-13810G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697741 | ||||||
| chr15:55697831
|
G | A | 87 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.398-13900C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697831 | ||||||
| chr15:55698005
|
T | C | 1 | a0004c0006t0101g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.398-14074A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698005 | ||||||
| chr15:55698209
|
T | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-14278A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698209 | ||||||
| chr15:55698404
|
T | C | 1 | a0001c0008t0038g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.398-14473A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698404 | ||||||
| chr15:55698520
|
A | G | 1 | a0001c0003t0019g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.398-14589T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698520 | ||||||
| chr15:55698566
|
C | T | 1 | a0009c0015t0044g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.398-14635G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698566 | ||||||
| chr15:55698860
|
G | C | 7 | a0001c0001t0033g0098a0002c0002t0074g0099a0003c0004t0031g0097others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-14929C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698860 | ||||||
| chr15:55698879
|
G | A | 14 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(11): Show | 14 | HG01081.hp2 HG01167.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-14948C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698879 | ||||||
| chr15:55698885
|
G | A | 1 | a0002c0002t0062g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.398-14954C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698885 | ||||||
| chr15:55699058
|
A | G | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-15127T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699058 | ||||||
| chr15:55699596
|
A | G | 1 | a0010c0014t0079g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.398-15665T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699596 | ||||||
| chr15:55699759
|
G | A | 14 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-15828C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699759 | ||||||
| chr15:55699976
|
T | G | 12 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-16045A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699976 | ||||||
| chr15:55700269
|
T | G | 51 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(48): Show | 51 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.398-16338A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700269 | ||||||
| chr15:55700447
|
A | G | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-16516T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700447 | ||||||
| chr15:55700464
|
T | G | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-16533A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700464 | ||||||
| chr15:55700676
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0086g0197 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.398-16745C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700676 | ||||||
| chr15:55700752
|
G | A | 7 | a0001c0001t0033g0098a0002c0002t0074g0099a0003c0004t0031g0097others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-16821C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700752 | ||||||
| chr15:55700762
|
C | T | 75 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(72): Show | 75 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-16831G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700762 | ||||||
| chr15:55700768
|
C | G | 1 | a0001c0001t0006g0162 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.398-16837G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700768 | ||||||
| chr15:55700916
|
G | A | 1 | a0002c0002t0098g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.398-16985C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700916 | ||||||
| chr15:55701118
|
T | C | 1 | a0001c0001t0107g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.398-17187A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701118 | ||||||
| chr15:55701163
|
T | C | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-17232A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701163 | ||||||
| chr15:55701244
|
T | G | 2 | a0006c0011t0036g0220a0006c0011t0108g0222 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.398-17313A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701244 | ||||||
| chr15:55701262
|
C | T | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-17331G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701262 | ||||||
| chr15:55701294
|
T | C | 10 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(7): Show | 10 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.398-17363A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701294 | ||||||
| chr15:55701398
|
G | C | 1 | a0002c0002t0003g0068 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.398-17467C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701398 | ||||||
| chr15:55701534
|
A | AAAAAC | 4 | a0001c0001t0034g0102a0001c0020t0058g0002a0002c0002t0099g0174others(1): Show | 4 | HG02145.hp2 HG02148.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-17608_398-1760 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701534 | ||||||
| chr15:55701607
|
C | T | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-17676G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701607 | ||||||
| chr15:55701617
|
A | C | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.398-17686T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701617 | ||||||
| chr15:55702059
|
T | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-18128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702059 | ||||||
| chr15:55702160
|
T | C | 94 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.398-18229A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702160 | ||||||
| chr15:55702239
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.398-18308G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702239 | ||||||
| chr15:55702274
|
G | A | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.398-18343C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702274 | ||||||
| chr15:55702387
|
C | CT | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-18457dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702387 | ||||||
| chr15:55702393
|
A | T | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-18462T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702393 | ||||||
| chr15:55702711
|
T | G | 94 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.398-18780A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702711 | ||||||
| chr15:55702933
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.398-19002T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702933 | ||||||
| chr15:55702945
|
G | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-19014C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702945 | ||||||
| chr15:55703116
|
G | C | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.398-19185C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703116 | ||||||
| chr15:55703146
|
T | C | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-19215A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703146 | ||||||
| chr15:55703344
|
G | A | 30 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(27): Show | 30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.398-19413C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703344 | ||||||
| chr15:55703439
|
C | T | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-19508G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703439 | ||||||
| chr15:55703489
|
T | C | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-19558A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703489 | ||||||
| chr15:55703595
|
T | C | 1 | a0001c0001t0110g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.398-19664A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703595 | ||||||
| chr15:55703911
|
G | A | 1 | a0002c0002t0029g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.398-19980C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703911 | ||||||
| chr15:55703932
|
T | C | 3 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0275 | 3 | HG01928.hp1 HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.398-20001A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703932 | ||||||
| chr15:55703937
|
C | T | 1 | a0002c0002t0029g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.398-20006G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703937 | ||||||
| chr15:55703940
|
G | A | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-20009C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703940 | ||||||
| chr15:55704007
|
G | GA | 46 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(43): Show | 46 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-20077dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704007 | ||||||
| chr15:55704072
|
G | A | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-20141C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704072 | ||||||
| chr15:55704358
|
T | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-20427A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704358 | ||||||
| chr15:55704504
|
G | C | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-20573C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704504 | ||||||
| chr15:55704528
|
C | T | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-20597G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704528 | ||||||
| chr15:55704587
|
T | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-20656A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704587 | ||||||
| chr15:55704609
|
G | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.398-20678C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704609 | ||||||
| chr15:55704637
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.398-20706T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704637 | ||||||
| chr15:55704898
|
A | T | 129 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(126): Show | 129 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.398-20967T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704898 | ||||||
| chr15:55704939
|
A | T | 1 | a0005c0010t0064g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.398-21008T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704939 | ||||||
| chr15:55704955
|
T | A | 1 | a0001c0007t0039g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.398-21024A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704955 | ||||||
| chr15:55705283
|
A | G | 2 | a0004c0006t0009g0015a0004c0006t0046g0012 | 2 | HG00733.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.398-21352T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705283 | ||||||
| chr15:55705346
|
A | T | 47 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.398-21415T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705346 | ||||||
| chr15:55705556
|
C | T | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-21625G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705556 | ||||||
| chr15:55705854
|
C | CT | 41 | a0001c0001t0001g0173a0001c0001t0001g0224a0001c0001t0002g0245others(38): Show | 41 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.398-21924dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705854 | ||||||
| chr15:55705854
|
C | CTT | 58 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.398-21925_398-2192 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705854 | ||||||
| chr15:55705882
|
G | T | 130 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(127): Show | 130 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.398-21951C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705882 | ||||||
| chr15:55705910
|
C | T | 1 | a0001c0001t0005g0164 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.398-21979G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705910 | ||||||
| chr15:55706014
|
A | ATTTT | 21 | a0001c0001t0036g0218a0001c0001t0107g0221a0001c0001t0110g0217others(18): Show | 21 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.398-22087_398-2208 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | ||||||
| chr15:55706014
|
A | ATTTTT | 56 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.398-22088_398-2208 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | ||||||
| chr15:55706014
|
A | ATTTTTT | 15 | a0001c0001t0002g0269a0001c0001t0002g0275a0001c0001t0004g0253others(12): Show | 15 | HG00323.hp2 HG00741.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.398-22089_398-2208 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | ||||||
| chr15:55706014
|
A | ATTTTTTT | 53 | a0001c0001t0011g0075a0001c0001t0019g0061a0001c0001t0023g0051others(50): Show | 53 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.398-22090_398-2208 others(11): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | ||||||
| chr15:55706014
|
A | ATTTTTTT others(1): Show |
28 | a0001c0001t0025g0013a0001c0001t0035g0001a0001c0001t0076g0133others(25): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.398-22091_398-2208 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | ||||||
| chr15:55706014
|
ATTT | A | 91 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.398-22086_398-2208 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | ||||||
| chr15:55706050
|
C | T | 47 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.398-22119G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706050 | ||||||
| chr15:55706098
|
C | G | 131 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(128): Show | 131 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.398-22167G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706098 | ||||||
| chr15:55706200
|
A | C | 1 | a0002c0002t0105g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.398-22269T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706200 | ||||||
| chr15:55706397
|
A | C | 131 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(128): Show | 131 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.398-22466T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706397 | ||||||
| chr15:55706405
|
C | T | 2 | a0001c0001t0004g0255a0012c0017t0002g0254 | 2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.398-22474G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706405 | ||||||
| chr15:55706539
|
G | A | 2 | a0001c0001t0034g0101a0001c0001t0034g0102 | 2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.398-22608C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706539 | ||||||
| chr15:55706582
|
CA | C | 31 | a0001c0001t0002g0241a0001c0001t0002g0269a0001c0001t0011g0075others(28): Show | 31 | HG00323.hp1 HG01081.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-22652delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706582 | ||||||
| chr15:55706582
|
CAA | C | 119 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0242others(116): Show | 120 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.398-22653_398-2265 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706582 | ||||||
| chr15:55706582
|
CAAAAAAA | C | 96 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.398-22658_398-2265 others(11): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706582 | ||||||
| chr15:55706659
|
AG | A | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-22729delC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706659 | ||||||
| chr15:55706784
|
G | A | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.398-22853C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706784 | ||||||
| chr15:55706863
|
A | G | 1 | a0007c0013t0004g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.398-22932T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706863 | ||||||
| chr15:55706958
|
G | C | 266 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.398-23027C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706958 | ||||||
| chr15:55707083
|
G | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-23152C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707083 | ||||||
| chr15:55707087
|
T | C | 31 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(28): Show | 31 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-23156A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707087 | ||||||
| chr15:55707234
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.398-23303G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707234 | ||||||
| chr15:55707277
|
C | T | 4 | a0002c0002t0003g0076a0005c0010t0026g0065a0005c0010t0064g0072others(1): Show | 4 | NA18944.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-23346G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707277 | ||||||
| chr15:55707296
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.398-23365T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707296 | ||||||
| chr15:55707499
|
G | A | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-23568C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707499 | ||||||
| chr15:55707747
|
A | G | 1 | a0001c0001t0059g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.398-23816T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707747 | ||||||
| chr15:55707865
|
C | T | 86 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-23934G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707865 | ||||||
| chr15:55707923
|
A | T | 1 | a0003c0004t0075g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398-23992T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707923 | ||||||
| chr15:55707985
|
T | G | 1 | a0001c0001t0091g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.398-24054A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707985 | ||||||
| chr15:55708034
|
G | A | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-24103C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708034 | ||||||
| chr15:55708148
|
T | TA | 51 | a0001c0001t0002g0238a0001c0001t0002g0248a0001c0001t0002g0249others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.398-24218dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAA | 18 | a0001c0001t0002g0240a0001c0001t0002g0242a0001c0001t0002g0265others(15): Show | 18 | HG00639.hp2 HG00741.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.398-24219_398-2421 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAA | 13 | a0001c0001t0002g0241a0001c0001t0002g0245a0001c0001t0002g0246others(10): Show | 13 | HG00438.hp2 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-24220_398-2421 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(2): Show |
10 | a0002c0002t0012g0016a0002c0002t0012g0028a0002c0002t0013g0020others(7): Show | 10 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.398-24226_398-2421 others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(3): Show |
5 | a0001c0001t0056g0004a0002c0002t0027g0023a0002c0002t0062g0025others(2): Show | 5 | HG01074.hp1 HG02055.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-24227_398-2421 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(4): Show |
5 | a0001c0001t0057g0006a0002c0002t0012g0018a0002c0002t0027g0029others(2): Show | 5 | HG00642.hp1 HG00642.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-24228_398-2421 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(5): Show |
3 | a0001c0001t0025g0030a0001c0001t0059g0005a0002c0002t0071g0014 | 3 | HG01433.hp1 HG01433.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.398-24229_398-2421 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(6): Show |
1 | a0002c0002t0061g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.398-24230_398-2421 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(7): Show |
1 | a0002c0002t0010g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.398-24231_398-2421 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(9): Show |
1 | a0001c0001t0025g0013 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.398-24233_398-2421 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
T | TAAAAAAA others(14): Show |
2 | a0002c0002t0010g0049a0002c0002t0010g0050 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.398-24238_398-2421 others(25): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
TAA | T | 6 | a0001c0001t0109g0232a0004c0005t0022g0041a0004c0005t0045g0040others(3): Show | 6 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-24219_398-2421 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
TAAA | T | 8 | a0001c0020t0058g0002a0004c0005t0048g0036a0004c0006t0009g0007others(5): Show | 8 | HG00733.hp2 HG01358.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-24220_398-2421 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0063g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.398-24227_398-2421 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0092g0127a0001c0001t0112g0128a0002c0002t0060g0046 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.398-24228_398-2421 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
TAAAAAAA others(6): Show |
T | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-24230_398-2421 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708148
|
TAAAAAAA others(10): Show |
T | 86 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-24234_398-2421 others(21): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | ||||||
| chr15:55708272
|
T | C | 101 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(98): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.398-24341A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708272 | ||||||
| chr15:55708361
|
C | T | 86 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-24430G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708361 | ||||||
| chr15:55708523
|
G | A | 30 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(27): Show | 30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.398-24592C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708523 | ||||||
| chr15:55708533
|
G | A | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-24602C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708533 | ||||||
| chr15:55708577
|
T | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-24646A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708577 | ||||||
| chr15:55708602
|
C | T | 27 | a0001c0001t0025g0013a0001c0001t0025g0030a0002c0002t0010g0048others(24): Show | 27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.398-24671G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708602 | ||||||
| chr15:55708996
|
A | G | 2 | a0001c0001t0023g0051a0001c0001t0023g0058 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.398-25065T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708996 | ||||||
| chr15:55709102
|
C | T | 6 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0187others(3): Show | 6 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-25171G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709102 | ||||||
| chr15:55709145
|
C | CA | 7 | a0001c0001t0002g0246a0001c0001t0004g0250a0001c0001t0017g0122others(4): Show | 7 | HG00438.hp2 HG01358.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-25215dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709145
|
C | CAAAAAAA others(4): Show |
4 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(1): Show | 4 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-25225_398-2521 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709145
|
C | CAAAAAAA others(5): Show |
1 | a0001c0007t0117g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.398-25226_398-2521 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709145
|
CA | C | 97 | a0001c0001t0002g0238a0001c0001t0002g0248a0001c0001t0002g0249others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.398-25215delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709145
|
CAA | C | 9 | a0001c0001t0002g0251a0001c0001t0025g0013a0001c0001t0025g0030others(6): Show | 9 | HG01109.hp1 HG01168.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-25216_398-2521 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709145
|
CAAA | C | 26 | a0001c0001t0056g0004a0001c0001t0059g0005a0001c0001t0106g0229others(23): Show | 26 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.398-25217_398-2521 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709145
|
CAAAAAA | C | 79 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.398-25220_398-2521 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709145
|
CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(6): Show | 9 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-25223_398-2521 others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | ||||||
| chr15:55709186
|
G | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-25255C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709186 | ||||||
| chr15:55709220
|
T | TAGTTA | 134 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.398-25290_398-2528 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709220 | ||||||
| chr15:55709314
|
T | C | 272 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.398-25383A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709314 | ||||||
| chr15:55709349
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398-25454_398-2541 others(40): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709349 | ||||||
| chr15:55709376
|
A | T | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-25445T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709376 | ||||||
| chr15:55709386
|
T | G | 16 | a0001c0001t0001g0165a0001c0001t0001g0182a0001c0001t0002g0273others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.398-25455A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709386 | ||||||
| chr15:55709388
|
T | G | 145 | a0001c0001t0001g0165a0001c0001t0001g0182a0001c0001t0001g0183others(142): Show | 145 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.398-25457A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709388 | ||||||
| chr15:55709390
|
G | T | 3 | a0001c0001t0014g0154a0001c0001t0085g0147a0001c0001t0087g0148 | 3 | HG02040.hp1 HG03669.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.398-25459C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709390 | ||||||
| chr15:55709401
|
C | T | 86 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-25470G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709401 | ||||||
| chr15:55709403
|
C | T | 13 | a0001c0001t0036g0218a0001c0001t0107g0221a0001c0001t0110g0217others(10): Show | 13 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-25472G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709403 | ||||||
| chr15:55709404
|
G | A | 1 | a0001c0001t0059g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.398-25473C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709404 | ||||||
| chr15:55709449
|
G | A | 1 | a0001c0001t0042g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.398-25518C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709449 | ||||||
| chr15:55709501
|
T | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-25570A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709501 | ||||||
| chr15:55709507
|
A | C | 9 | a0001c0003t0003g0042a0001c0003t0003g0069a0001c0003t0003g0073others(6): Show | 9 | HG00280.hp1 HG00408.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-25576T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709507 | ||||||
| chr15:55709550
|
G | A | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.398-25619C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709550 | ||||||
| chr15:55709576
|
C | T | 134 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.398-25645G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709576 | ||||||
| chr15:55709759
|
T | C | 243 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.398-25828A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709759 | ||||||
| chr15:55709771
|
C | A | 264 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.398-25840G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709771 | ||||||
| chr15:55709837
|
G | A | 4 | a0002c0002t0003g0076a0005c0010t0026g0065a0005c0010t0064g0072others(1): Show | 4 | NA18944.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-25906C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709837 | ||||||
| chr15:55710035
|
A | C | 1 | a0001c0001t0110g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.398-26104T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710035 | ||||||
| chr15:55710038
|
C | T | 1 | a0001c0001t0111g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.398-26107G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710038 | ||||||
| chr15:55710210
|
G | C | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-26279C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710210 | ||||||
| chr15:55710300
|
A | G | 3 | a0001c0001t0033g0103a0001c0001t0034g0101a0001c0001t0034g0102 | 3 | HG02965.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-26369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710300 | ||||||
| chr15:55710325
|
A | T | 1 | a0001c0001t0115g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.398-26394T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710325 | ||||||
| chr15:55710621
|
C | T | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-26690G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710621 | ||||||
| chr15:55710698
|
TAA | T | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-26769_398-2676 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710698 | ||||||
| chr15:55710709
|
G | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-26778C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710709 | ||||||
| chr15:55710821
|
T | C | 78 | a0001c0001t0001g0171a0001c0001t0002g0238a0001c0001t0002g0240others(75): Show | 78 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.398-26890A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710821 | ||||||
| chr15:55710938
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.398-27007G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710938 | ||||||
| chr15:55710943
|
G | C | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-27012C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710943 | ||||||
| chr15:55711002
|
G | A | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-27071C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711002 | ||||||
| chr15:55711081
|
A | AT | 36 | a0001c0001t0002g0238a0001c0001t0002g0261a0001c0001t0002g0269others(33): Show | 36 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.398-27151dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711081 | ||||||
| chr15:55711081
|
A | ATT | 6 | a0001c0001t0002g0275a0001c0001t0059g0005a0001c0007t0118g0111others(3): Show | 6 | HG02145.hp2 HG02148.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-27152_398-2715 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711081 | ||||||
| chr15:55711081
|
AT | A | 55 | a0001c0001t0001g0176a0001c0001t0011g0075a0001c0001t0011g0091others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.398-27151delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711081 | ||||||
| chr15:55711168
|
TG | T | 57 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.398-27238delC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711168 | ||||||
| chr15:55711218
|
G | T | 1 | a0010c0014t0079g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.398-27287C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711218 | ||||||
| chr15:55711323
|
A | G | 1 | a0002c0002t0028g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.398-27392T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711323 | ||||||
| chr15:55711507
|
A | G | 135 | a0001c0001t0001g0171a0001c0001t0002g0238a0001c0001t0002g0240others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.398-27576T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711507 | ||||||
| chr15:55711511
|
G | C | 3 | a0001c0001t0106g0229a0001c0001t0109g0232a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.398-27580C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711511 | ||||||
| chr15:55711654
|
T | G | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-27723A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711654 | ||||||
| chr15:55711718
|
T | TA | 26 | a0001c0001t0025g0013a0001c0001t0025g0030a0002c0002t0010g0048others(23): Show | 26 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.398-27788dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711718 | ||||||
| chr15:55711814
|
G | A | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-27883C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711814 | ||||||
| chr15:55712020
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.398-28089T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712020 | ||||||
| chr15:55712026
|
T | A | 3 | a0001c0007t0116g0109a0001c0007t0117g0110a0001c0007t0118g0111 | 3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.398-28095A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712026 | ||||||
| chr15:55712061
|
T | G | 4 | a0002c0002t0114g0215a0006c0011t0036g0220a0006c0011t0104g0219others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-28130A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712061 | ||||||
| chr15:55712152
|
A | G | 2 | a0001c0020t0058g0002a0011c0019t0051g0003 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.398-28221T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712152 | ||||||
| chr15:55712216
|
G | A | 1 | a0001c0003t0003g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.397+28166C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712216 | ||||||
| chr15:55712424
|
AC | A | 6 | a0001c0001t0033g0098a0002c0002t0074g0099a0003c0004t0031g0097others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+27957delG | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712424 | ||||||
| chr15:55712443
|
A | G | 54 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.397+27939T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712443 | ||||||
| chr15:55712522
|
T | TA | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+27859dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712522 | ||||||
| chr15:55712629
|
A | G | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+27753T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712629 | ||||||
| chr15:55712909
|
G | A | 86 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.397+27473C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712909 | ||||||
| chr15:55713137
|
TTTATAA | T | 135 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.397+27239_397+2724 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713137 | ||||||
| chr15:55713160
|
G | A | 1 | a0002c0002t0029g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.397+27222C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713160 | ||||||
| chr15:55713325
|
C | A | 53 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(50): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.397+27057G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713325 | ||||||
| chr15:55713386
|
C | T | 30 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(27): Show | 30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+26996G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713386 | ||||||
| chr15:55713497
|
A | G | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+26885T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713497 | ||||||
| chr15:55713534
|
C | G | 83 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.397+26848G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713534 | ||||||
| chr15:55713557
|
A | T | 2 | a0001c0001t0001g0186a0001c0001t0084g0192 | 2 | NA18973.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.397+26825T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713557 | ||||||
| chr15:55713593
|
T | A | 87 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.397+26789A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713593 | ||||||
| chr15:55713728
|
T | C | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+26654A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713728 | ||||||
| chr15:55713733
|
A | AT | 140 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(137): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.397+26648dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713733 | ||||||
| chr15:55714067
|
T | G | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.397+26315A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714067 | ||||||
| chr15:55714157
|
C | T | 1 | a0001c0001t0011g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.397+26225G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714157 | ||||||
| chr15:55714205
|
G | GTC | 12 | a0001c0001t0001g0106a0001c0001t0004g0250a0001c0008t0038g0209others(9): Show | 12 | HG01358.hp1 HG01515.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+26175_397+2617 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
G | GTCTCTC | 27 | a0001c0001t0002g0248a0001c0001t0002g0251a0001c0001t0004g0247others(24): Show | 27 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.397+26171_397+2617 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
G | GTCTCTCT others(1): Show |
38 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(35): Show | 38 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.397+26169_397+2617 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
G | GTCTCTCT others(3): Show |
24 | a0001c0001t0002g0238a0001c0001t0002g0261a0001c0001t0019g0061others(21): Show | 24 | HG00642.hp2 HG01361.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.397+26167_397+2617 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
G | GTCTCTCT others(5): Show |
39 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0025g0030others(36): Show | 40 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.397+26165_397+2617 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
G | GTCTCTCT others(7): Show |
6 | a0002c0002t0003g0076a0002c0002t0010g0048a0002c0002t0013g0024others(3): Show | 6 | HG01257.hp1 HG02486.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+26163_397+2617 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
G | GTCTCTCT others(9): Show |
5 | a0001c0001t0056g0004a0001c0001t0059g0005a0001c0001t0109g0232others(2): Show | 5 | HG00280.hp1 HG02818.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+26161_397+2617 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
G | GTCTCTCT others(13): Show |
1 | a0001c0001t0057g0006 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.397+26157_397+2617 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714205
|
GTCTCTC | G | 11 | a0001c0001t0036g0218a0001c0001t0107g0221a0001c0001t0110g0217others(8): Show | 11 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+26171_397+2617 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | ||||||
| chr15:55714297
|
T | C | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+26085A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714297 | ||||||
| chr15:55714387
|
C | T | 1 | a0002c0002t0011g0084 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.397+25995G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714387 | ||||||
| chr15:55714389
|
C | T | 48 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(45): Show | 48 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.397+25993G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714389 | ||||||
| chr15:55714390
|
G | C | 6 | a0003c0004t0024g0056a0003c0004t0024g0057a0003c0004t0052g0059others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+25992C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714390 | ||||||
| chr15:55714473
|
C | T | 1 | a0001c0001t0019g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.397+25909G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714473 | ||||||
| chr15:55714543
|
C | A | 27 | a0001c0001t0025g0013a0001c0001t0025g0030a0002c0002t0010g0048others(24): Show | 27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.397+25839G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714543 | ||||||
| chr15:55714806
|
C | T | 139 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.397+25576G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714806 | ||||||
| chr15:55715004
|
A | G | 16 | a0001c0001t0033g0103a0001c0001t0034g0101a0001c0001t0034g0102others(13): Show | 16 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.397+25378T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715004 | ||||||
| chr15:55715009
|
A | T | 3 | a0001c0007t0116g0109a0001c0007t0117g0110a0001c0007t0118g0111 | 3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.397+25373T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715009 | ||||||
| chr15:55715050
|
C | G | 1 | a0005c0010t0064g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.397+25332G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715050 | ||||||
| chr15:55715081
|
A | G | 1 | a0002c0002t0066g0083 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.397+25301T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715081 | ||||||
| chr15:55715168
|
T | C | 282 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.397+25214A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715168 | ||||||
| chr15:55715402
|
T | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+24980A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715402 | ||||||
| chr15:55715497
|
T | C | 16 | a0001c0001t0001g0224a0001c0003t0005g0191a0001c0003t0005g0225others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.397+24885A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715497 | ||||||
| chr15:55715716
|
T | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+24666A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715716 | ||||||
| chr15:55715723
|
T | G | 1 | a0003c0004t0053g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.397+24659A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715723 | ||||||
| chr15:55715917
|
A | C | 1 | a0002c0002t0017g0126 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.397+24465T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715917 | ||||||
| chr15:55716113
|
G | A | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.397+24269C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716113 | ||||||
| chr15:55716139
|
G | C | 1 | a0001c0001t0008g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.397+24243C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716139 | ||||||
| chr15:55716227
|
T | C | 15 | a0001c0001t0106g0229a0001c0001t0111g0228a0001c0020t0058g0002others(12): Show | 15 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+24155A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716227 | ||||||
| chr15:55716357
|
T | C | 2 | a0001c0001t0004g0255a0012c0017t0002g0254 | 2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.397+24025A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716357 | ||||||
| chr15:55716425
|
C | T | 1 | a0001c0001t0086g0197 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.397+23957G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716425 | ||||||
| chr15:55716509
|
G | C | 2 | a0001c0020t0058g0002a0011c0019t0051g0003 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+23873C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716509 | ||||||
| chr15:55716565
|
T | C | 1 | a0002c0002t0010g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.397+23817A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716565 | ||||||
| chr15:55716781
|
G | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+23601C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716781 | ||||||
| chr15:55716802
|
T | C | 30 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(27): Show | 30 | HG02145.hp1 HG02257.hp2 HG02572.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+23580A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716802 | ||||||
| chr15:55716821
|
T | C | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+23561A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716821 | ||||||
| chr15:55716848
|
T | C | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397+23534A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716848 | ||||||
| chr15:55716928
|
G | C | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397+23454C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716928 | ||||||
| chr15:55716957
|
G | A | 1 | a0008c0021t0102g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.397+23425C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716957 | ||||||
| chr15:55716980
|
T | C | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.397+23402A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716980 | ||||||
| chr15:55716996
|
G | A | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+23386C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716996 | ||||||
| chr15:55717446
|
C | T | 1 | a0002c0002t0100g0214 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.397+22936G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717446 | ||||||
| chr15:55717450
|
A | T | 84 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.397+22932T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717450 | ||||||
| chr15:55717745
|
C | G | 2 | a0001c0001t0002g0261a0001c0001t0043g0260 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.397+22637G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717745 | ||||||
| chr15:55717756
|
A | G | 48 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(45): Show | 48 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.397+22626T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717756 | ||||||
| chr15:55718084
|
T | C | 2 | a0001c0001t0004g0281a0001c0001t0004g0282 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.397+22298A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718084 | ||||||
| chr15:55718433
|
C | T | 282 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.397+21949G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718433 | ||||||
| chr15:55718482
|
A | C | 28 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0109g0232others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.397+21900T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718482 | ||||||
| chr15:55718609
|
G | C | 12 | a0001c0001t0036g0218a0001c0001t0107g0221a0001c0001t0110g0217others(9): Show | 12 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+21773C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718609 | ||||||
| chr15:55718617
|
C | CA | 9 | a0001c0001t0033g0098a0001c0001t0033g0103a0001c0001t0034g0101others(6): Show | 9 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+21764dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718617 | ||||||
| chr15:55718628
|
C | CA | 61 | a0001c0001t0001g0151a0001c0001t0002g0238a0001c0001t0002g0240others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.397+21753dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718628 | ||||||
| chr15:55718632
|
A | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0173a0010c0014t0079g0234 | 3 | HG02683.hp2 NA19003.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.397+21750T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718632 | ||||||
| chr15:55718675
|
T | C | 30 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(27): Show | 30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+21707A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718675 | ||||||
| chr15:55718690
|
T | A | 2 | a0006c0011t0036g0220a0006c0011t0108g0222 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.397+21692A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718690 | ||||||
| chr15:55718904
|
G | A | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.397+21478C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718904 | ||||||
| chr15:55718909
|
A | AT | 54 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.397+21472dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718909 | ||||||
| chr15:55719025
|
A | G | 261 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.397+21357T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719025 | ||||||
| chr15:55719171
|
G | A | 5 | a0001c0001t0025g0030a0002c0002t0012g0018a0002c0002t0012g0028others(2): Show | 5 | HG00642.hp2 HG01433.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+21211C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719171 | ||||||
| chr15:55719227
|
T | A | 1 | a0003c0004t0031g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+21155A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719227 | ||||||
| chr15:55719392
|
T | C | 2 | a0001c0001t0037g0169a0001c0001t0037g0172 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.397+20990A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719392 | ||||||
| chr15:55719757
|
G | T | 1 | a0001c0001t0093g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.397+20625C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719757 | ||||||
| chr15:55719792
|
C | G | 2 | a0001c0001t0037g0169a0001c0001t0037g0172 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.397+20590G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719792 | ||||||
| chr15:55719817
|
C | T | 27 | a0001c0001t0025g0013a0001c0001t0025g0030a0002c0002t0010g0048others(24): Show | 27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.397+20565G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719817 | ||||||
| chr15:55719906
|
A | C | 2 | a0001c0001t0025g0013a0002c0002t0071g0014 | 2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.397+20476T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719906 | ||||||
| chr15:55719919
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.397+20463C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719919 | ||||||
| chr15:55719929
|
G | T | 53 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(50): Show | 53 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.397+20453C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719929 | ||||||
| chr15:55720060
|
AAAAAG | A | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+20317_397+2032 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720060 | ||||||
| chr15:55720188
|
G | A | 1 | a0001c0001t0035g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.397+20194C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720188 | ||||||
| chr15:55720391
|
A | T | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+19991T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720391 | ||||||
| chr15:55720488
|
T | C | 30 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(27): Show | 30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+19894A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720488 | ||||||
| chr15:55720508
|
T | A | 141 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.397+19874A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720508 | ||||||
| chr15:55720713
|
C | A | 1 | a0001c0007t0039g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.397+19669G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720713 | ||||||
| chr15:55720713
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+19669G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720713 | ||||||
| chr15:55720850
|
T | C | 1 | a0001c0001t0089g0202 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.397+19532A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720850 | ||||||
| chr15:55721065
|
G | A | 30 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(27): Show | 30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+19317C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721065 | ||||||
| chr15:55721113
|
G | T | 2 | a0001c0020t0058g0002a0011c0019t0051g0003 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+19269C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721113 | ||||||
| chr15:55721279
|
C | A | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+19103G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721279 | ||||||
| chr15:55721387
|
G | A | 2 | a0001c0001t0092g0127a0001c0001t0112g0128 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.397+18995C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721387 | ||||||
| chr15:55721453
|
A | T | 2 | a0001c0001t0033g0098a0002c0002t0074g0099 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.397+18929T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721453 | ||||||
| chr15:55721607
|
C | T | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+18775G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721607 | ||||||
| chr15:55721723
|
C | T | 139 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.397+18659G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721723 | ||||||
| chr15:55721911
|
A | G | 1 | a0001c0001t0023g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.397+18471T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721911 | ||||||
| chr15:55721927
|
T | A | 1 | a0001c0001t0004g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.397+18455A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721927 | ||||||
| chr15:55722074
|
A | G | 1 | a0002c0002t0067g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.397+18308T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722074 | ||||||
| chr15:55722151
|
A | C | 1 | a0001c0009t0049g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.397+18231T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722151 | ||||||
| chr15:55722153
|
G | A | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+18229C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722153 | ||||||
| chr15:55722183
|
C | T | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+18199G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722183 | ||||||
| chr15:55722229
|
T | A | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+18153A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722229 | ||||||
| chr15:55722285
|
G | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0001t0014g0167others(4): Show | 7 | NA18942.hp2 NA18944.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+18097C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722285 | ||||||
| chr15:55722407
|
AATAACT | A | 47 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.397+17969_397+1797 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722407 | ||||||
| chr15:55722480
|
T | C | 1 | a0002c0002t0105g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.397+17902A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722480 | ||||||
| chr15:55722538
|
T | C | 49 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+17844A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722538 | ||||||
| chr15:55722585
|
CAG | C | 3 | a0001c0001t0030g0092a0001c0001t0072g0094a0013c0016t0030g0093 | 3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.397+17795_397+1779 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722585 | ||||||
| chr15:55722785
|
T | TG | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+17596dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722785 | ||||||
| chr15:55722984
|
G | A | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+17398C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722984 | ||||||
| chr15:55723254
|
T | C | 1 | a0001c0001t0019g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.397+17128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723254 | ||||||
| chr15:55723392
|
T | TA | 31 | a0001c0001t0006g0162a0001c0001t0025g0013a0001c0001t0025g0030others(28): Show | 31 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.397+16989dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723392 | ||||||
| chr15:55723569
|
T | C | 85 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(82): Show | 85 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.397+16813A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723569 | ||||||
| chr15:55723730
|
T | C | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+16652A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723730 | ||||||
| chr15:55723736
|
T | A | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+16646A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723736 | ||||||
| chr15:55723752
|
C | CT | 122 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0170others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.397+16629dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723752 | ||||||
| chr15:55723752
|
C | CTT | 26 | a0001c0001t0004g0281a0001c0001t0004g0282a0001c0001t0025g0030others(23): Show | 26 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.397+16628_397+1662 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723752 | ||||||
| chr15:55723783
|
G | A | 1 | a0001c0001t0122g0278 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.397+16599C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723783 | ||||||
| chr15:55724005
|
C | G | 1 | a0002c0002t0067g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.397+16377G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724005 | ||||||
| chr15:55724110
|
C | T | 2 | a0001c0001t0002g0249a0001c0001t0002g0257 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.397+16272G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724110 | ||||||
| chr15:55724226
|
C | G | 1 | a0005c0010t0064g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.397+16156G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724226 | ||||||
| chr15:55724281
|
G | A | 7 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+16101C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724281 | ||||||
| chr15:55724324
|
G | A | 1 | a0002c0002t0120g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.397+16058C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724324 | ||||||
| chr15:55724548
|
T | C | 47 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.397+15834A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724548 | ||||||
| chr15:55724551
|
G | A | 1 | a0013c0016t0030g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.397+15831C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724551 | ||||||
| chr15:55724601
|
G | T | 6 | a0001c0001t0109g0232a0001c0007t0039g0230a0001c0007t0039g0231others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+15781C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724601 | ||||||
| chr15:55724616
|
A | G | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+15766T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724616 | ||||||
| chr15:55724629
|
C | A | 1 | a0004c0005t0048g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.397+15753G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724629 | ||||||
| chr15:55724699
|
G | A | 5 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(2): Show | 5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+15683C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724699 | ||||||
| chr15:55724768
|
AAAAAT | A | 58 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+15609_397+1561 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724768 | ||||||
| chr15:55724955
|
G | A | 1 | a0002c0002t0098g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.397+15427C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724955 | ||||||
| chr15:55725224
|
T | C | 59 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.397+15158A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725224 | ||||||
| chr15:55725357
|
T | G | 2 | a0002c0002t0005g0108a0002c0002t0005g0216 | 2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.397+15025A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725357 | ||||||
| chr15:55725413
|
A | G | 1 | a0001c0001t0072g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.397+14969T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725413 | ||||||
| chr15:55725676
|
A | G | 1 | a0001c0001t0017g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.397+14706T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725676 | ||||||
| chr15:55725745
|
T | G | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+14637A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725745 | ||||||
| chr15:55725895
|
C | T | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+14487G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725895 | ||||||
| chr15:55725896
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0084g0192 | 2 | NA18973.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.397+14486C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725896 | ||||||
| chr15:55726005
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.397+14377C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726005 | ||||||
| chr15:55726089
|
C | T | 1 | a0002c0002t0121g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.397+14293G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726089 | ||||||
| chr15:55726187
|
C | T | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+14195G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726187 | ||||||
| chr15:55726395
|
C | A | 1 | a0001c0003t0005g0225 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.397+13987G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726395 | ||||||
| chr15:55726403
|
G | A | 1 | a0007c0013t0004g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.397+13979C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726403 | ||||||
| chr15:55726617
|
G | A | 5 | a0001c0001t0033g0098a0002c0002t0074g0099a0003c0004t0032g0095others(2): Show | 5 | HG02622.hp2 HG03195.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+13765C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726617 | ||||||
| chr15:55726621
|
A | G | 1 | a0001c0001t0043g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.397+13761T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726621 | ||||||
| chr15:55726641
|
C | CA | 17 | a0001c0001t0002g0246a0001c0001t0002g0269a0001c0001t0004g0253others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+13740dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726641 | ||||||
| chr15:55726641
|
CA | C | 63 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.397+13740delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726641 | ||||||
| chr15:55726658
|
T | A | 45 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.397+13724A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726658 | ||||||
| chr15:55726899
|
G | A | 1 | a0003c0004t0032g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.397+13483C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726899 | ||||||
| chr15:55726950
|
CA | C | 186 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(183): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.397+13431delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726950 | ||||||
| chr15:55726959
|
A | G | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+13423T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726959 | ||||||
| chr15:55727168
|
T | C | 1 | a0010c0014t0079g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.397+13214A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727168 | ||||||
| chr15:55727455
|
T | C | 55 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+12927A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727455 | ||||||
| chr15:55727579
|
T | C | 17 | a0001c0001t0033g0103a0001c0001t0034g0101a0001c0001t0034g0102others(14): Show | 17 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+12803A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727579 | ||||||
| chr15:55727697
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.397+12685C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727697 | ||||||
| chr15:55727723
|
C | T | 3 | a0001c0003t0003g0042a0001c0003t0003g0073a0001c0003t0003g0080 | 3 | HG01943.hp1 HG01981.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.397+12659G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727723 | ||||||
| chr15:55727752
|
C | T | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+12630G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727752 | ||||||
| chr15:55727887
|
G | A | 6 | a0001c0001t0109g0232a0001c0007t0039g0230a0001c0007t0039g0231others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+12495C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727887 | ||||||
| chr15:55727957
|
C | A | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+12425G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727957 | ||||||
| chr15:55727979
|
C | G | 6 | a0001c0001t0033g0098a0002c0002t0074g0099a0003c0004t0031g0097others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+12403G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727979 | ||||||
| chr15:55728108
|
C | T | 1 | a0003c0004t0031g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+12274G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728108 | ||||||
| chr15:55728117
|
C | T | 55 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+12265G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728117 | ||||||
| chr15:55728221
|
C | A | 1 | a0001c0001t0059g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.397+12161G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728221 | ||||||
| chr15:55728521
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0203 | 2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.397+11861A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728521 | ||||||
| chr15:55728529
|
A | AG | 55 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+11852dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728529 | ||||||
| chr15:55728659
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.397+11723T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728659 | ||||||
| chr15:55728722
|
T | C | 1 | a0002c0002t0061g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.397+11660A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728722 | ||||||
| chr15:55728729
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397+11653A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728729 | ||||||
| chr15:55728766
|
A | AG | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+11615_397+1161 others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728766 | ||||||
| chr15:55728770
|
A | C | 273 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+11612T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728770 | ||||||
| chr15:55728808
|
T | C | 79 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(76): Show | 79 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.397+11574A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728808 | ||||||
| chr15:55728821
|
T | C | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+11561A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728821 | ||||||
| chr15:55728959
|
G | A | 1 | a0012c0017t0002g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.397+11423C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728959 | ||||||
| chr15:55728975
|
T | C | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+11407A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728975 | ||||||
| chr15:55728980
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+11402G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728980 | ||||||
| chr15:55729003
|
A | G | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+11379T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729003 | ||||||
| chr15:55729141
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0087g0148 | 2 | HG02040.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.397+11241C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729141 | ||||||
| chr15:55729223
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0206a0001c0001t0008g0207 | 3 | NA18948.hp2 NA18980.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.397+11159C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729223 | ||||||
| chr15:55729232
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.397+11150G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729232 | ||||||
| chr15:55729596
|
T | A | 57 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+10786A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729596 | ||||||
| chr15:55729598
|
A | T | 10 | a0002c0002t0020g0052a0002c0002t0020g0060a0002c0002t0021g0010others(7): Show | 10 | HG01255.hp2 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.397+10784T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729598 | ||||||
| chr15:55729739
|
C | A | 1 | a0001c0003t0003g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.397+10643G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729739 | ||||||
| chr15:55729748
|
T | G | 4 | a0002c0002t0005g0117a0002c0002t0005g0118a0002c0002t0005g0119others(1): Show | 4 | NA18964.hp1 NA18981.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+10634A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729748 | ||||||
| chr15:55729908
|
G | A | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+10474C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729908 | ||||||
| chr15:55729943
|
G | A | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+10439C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729943 | ||||||
| chr15:55730028
|
T | C | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+10354A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730028 | ||||||
| chr15:55730126
|
G | A | 81 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.397+10256C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730126 | ||||||
| chr15:55730159
|
C | A | 1 | a0001c0001t0042g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.397+10223G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730159 | ||||||
| chr15:55730584
|
C | T | 1 | a0002c0002t0121g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.397+9798G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730584 | ||||||
| chr15:55730595
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.397+9787A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730595 | ||||||
| chr15:55730730
|
G | T | 79 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(76): Show | 79 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.397+9652C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730730 | ||||||
| chr15:55730751
|
G | C | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+9631C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730751 | ||||||
| chr15:55730792
|
ACT | A | 6 | a0001c0001t0109g0232a0001c0007t0039g0230a0001c0007t0039g0231others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+9588_397+9589d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730792 | ||||||
| chr15:55731027
|
A | T | 1 | a0001c0001t0085g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.397+9355T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731027 | ||||||
| chr15:55731031
|
A | G | 1 | a0002c0002t0010g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.397+9351T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731031 | ||||||
| chr15:55731098
|
G | C | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.397+9284C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731098 | ||||||
| chr15:55731115
|
A | ACTTT | 137 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(134): Show | 137 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.397+9263_397+9266d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731115 | ||||||
| chr15:55731234
|
C | CTCT | 58 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+9145_397+9147d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731234 | ||||||
| chr15:55731245
|
G | C | 9 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0092g0127others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+9137C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731245 | ||||||
| chr15:55731304
|
G | T | 243 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.397+9078C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731304 | ||||||
| chr15:55731359
|
TATCA | T | 6 | a0001c0001t0109g0232a0001c0007t0039g0230a0001c0007t0039g0231others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+9019_397+9022d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731359 | ||||||
| chr15:55731366
|
C | CT | 49 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0170others(46): Show | 49 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.397+9015dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | ||||||
| chr15:55731366
|
C | CTT | 69 | a0001c0001t0006g0163a0001c0001t0011g0075a0001c0001t0017g0122others(66): Show | 69 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.397+9014_397+9015d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | ||||||
| chr15:55731366
|
C | CTTT | 10 | a0001c0001t0019g0061a0002c0002t0003g0067a0002c0002t0003g0071others(7): Show | 10 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+9013_397+9015d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | ||||||
| chr15:55731366
|
CT | C | 6 | a0001c0001t0001g0195a0001c0001t0002g0251a0001c0001t0002g0277others(3): Show | 6 | HG01074.hp2 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+9015delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | ||||||
| chr15:55731410
|
G | A | 1 | a0001c0001t0087g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.397+8972C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731410 | ||||||
| chr15:55731418
|
TGGAGTAC others(3): Show |
T | 1 | a0001c0001t0042g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.397+8954_397+8963d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731418 | ||||||
| chr15:55731440
|
G | A | 1 | a0001c0001t0107g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.397+8942C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731440 | ||||||
| chr15:55731502
|
C | T | 4 | a0001c0001t0030g0092a0001c0001t0072g0094a0002c0002t0021g0010others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+8880G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731502 | ||||||
| chr15:55731573
|
G | A | 136 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.397+8809C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731573 | ||||||
| chr15:55731575
|
C | T | 241 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.397+8807G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731575 | ||||||
| chr15:55731711
|
C | T | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+8671G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731711 | ||||||
| chr15:55731717
|
A | C | 57 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+8665T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731717 | ||||||
| chr15:55731864
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.397+8518A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731864 | ||||||
| chr15:55731892
|
C | A | 7 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(4): Show | 7 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+8490G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731892 | ||||||
| chr15:55731968
|
C | A | 1 | a0004c0006t0009g0015 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.397+8414G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731968 | ||||||
| chr15:55732031
|
C | T | 243 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.397+8351G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732031 | ||||||
| chr15:55732069
|
T | C | 90 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.397+8313A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732069 | ||||||
| chr15:55732133
|
A | G | 1 | a0001c0009t0097g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.397+8249T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732133 | ||||||
| chr15:55732348
|
C | A | 1 | a0002c0002t0012g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+8034G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732348 | ||||||
| chr15:55732493
|
C | CT | 211 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.397+7888dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732493 | ||||||
| chr15:55732493
|
C | CTT | 9 | a0001c0001t0001g0149a0001c0001t0001g0186a0001c0001t0001g0196others(6): Show | 9 | HG00738.hp1 HG01978.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+7887_397+7888d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732493 | ||||||
| chr15:55732736
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.397+7646G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732736 | ||||||
| chr15:55732804
|
T | A | 1 | a0004c0006t0046g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.397+7578A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732804 | ||||||
| chr15:55732909
|
C | T | 1 | a0002c0002t0003g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.397+7473G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732909 | ||||||
| chr15:55732990
|
C | T | 282 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.397+7392G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732990 | ||||||
| chr15:55732991
|
C | T | 1 | a0002c0002t0021g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.397+7391G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732991 | ||||||
| chr15:55733124
|
G | A | 1 | a0001c0001t0115g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.397+7258C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733124 | ||||||
| chr15:55733214
|
T | C | 55 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+7168A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733214 | ||||||
| chr15:55733276
|
T | G | 2 | a0001c0001t0033g0098a0002c0002t0074g0099 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.397+7106A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733276 | ||||||
| chr15:55733378
|
C | T | 3 | a0001c0012t0078g0113a0001c0012t0080g0114a0002c0002t0011g0084 | 3 | HG02630.hp2 HG03453.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.397+7004G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733378 | ||||||
| chr15:55733433
|
C | G | 1 | a0005c0010t0064g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.397+6949G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733433 | ||||||
| chr15:55733514
|
C | CA | 73 | a0001c0001t0001g0106a0001c0001t0001g0200a0001c0001t0001g0203others(70): Show | 74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.397+6867dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733514 | ||||||
| chr15:55733514
|
CA | C | 7 | a0001c0001t0004g0243a0001c0001t0033g0098a0002c0002t0027g0029others(4): Show | 7 | HG00639.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+6867delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733514 | ||||||
| chr15:55733514
|
CAA | C | 20 | a0001c0001t0025g0013a0001c0001t0025g0030a0002c0002t0012g0016others(17): Show | 20 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.397+6866_397+6867d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733514 | ||||||
| chr15:55733573
|
T | C | 14 | a0001c0001t0036g0218a0001c0001t0107g0221a0001c0001t0110g0217others(11): Show | 14 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.397+6809A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733573 | ||||||
| chr15:55733622
|
T | C | 2 | a0001c0020t0058g0002a0011c0019t0051g0003 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+6760A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733622 | ||||||
| chr15:55733698
|
G | A | 2 | a0002c0002t0005g0108a0002c0002t0005g0216 | 2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.397+6684C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733698 | ||||||
| chr15:55733720
|
G | C | 1 | a0001c0001t0025g0030 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.397+6662C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733720 | ||||||
| chr15:55733853
|
C | A | 14 | a0001c0001t0001g0161a0001c0001t0001g0179a0001c0001t0001g0183others(11): Show | 14 | HG01074.hp2 HG01109.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.397+6529G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733853 | ||||||
| chr15:55733892
|
G | A | 1 | a0002c0002t0062g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.397+6490C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733892 | ||||||
| chr15:55734075
|
G | A | 1 | a0002c0002t0007g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.397+6307C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734075 | ||||||
| chr15:55734214
|
C | T | 57 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+6168G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734214 | ||||||
| chr15:55734508
|
T | A | 2 | a0001c0001t0092g0127a0001c0001t0112g0128 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.397+5874A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734508 | ||||||
| chr15:55734618
|
T | C | 1 | a0001c0009t0049g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.397+5764A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734618 | ||||||
| chr15:55734748
|
TA | T | 274 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.397+5633delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734748 | ||||||
| chr15:55734930
|
A | G | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+5452T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734930 | ||||||
| chr15:55734938
|
T | C | 5 | a0001c0007t0039g0230a0001c0007t0039g0231a0001c0007t0116g0109others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+5444A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734938 | ||||||
| chr15:55734966
|
T | A | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+5416A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734966 | ||||||
| chr15:55734990
|
T | C | 7 | a0001c0001t0001g0165a0001c0001t0001g0181a0001c0001t0001g0182others(4): Show | 7 | HG00408.hp1 NA18954.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+5392A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734990 | ||||||
| chr15:55735111
|
T | C | 83 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.397+5271A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735111 | ||||||
| chr15:55735116
|
A | C | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.397+5266T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735116 | ||||||
| chr15:55735269
|
A | G | 1 | a0002c0002t0017g0126 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.397+5113T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735269 | ||||||
| chr15:55735312
|
T | C | 58 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+5070A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735312 | ||||||
| chr15:55735420
|
CTAAAACC others(5): Show |
C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+4950_397+4961d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735420 | ||||||
| chr15:55735532
|
A | T | 1 | a0001c0001t0002g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.397+4850T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735532 | ||||||
| chr15:55735718
|
T | TA | 85 | a0001c0001t0001g0107a0001c0001t0001g0183a0001c0001t0002g0238others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.397+4663dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | ||||||
| chr15:55735718
|
T | TAA | 13 | a0001c0001t0002g0257a0001c0001t0002g0261a0001c0001t0002g0270others(10): Show | 13 | HG01891.hp2 HG01943.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+4662_397+4663d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | ||||||
| chr15:55735718
|
T | TAAA | 11 | a0001c0001t0034g0102a0001c0001t0059g0005a0001c0001t0107g0221others(8): Show | 11 | HG00323.hp1 HG02818.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+4661_397+4663d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | ||||||
| chr15:55735718
|
T | TAAAA | 44 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(41): Show | 44 | HG00280.hp1 HG00323.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.397+4660_397+4663d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | ||||||
| chr15:55735718
|
T | TAAAAA | 18 | a0001c0001t0023g0058a0001c0001t0033g0103a0001c0003t0003g0089others(15): Show | 18 | HG00408.hp2 HG00438.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.397+4659_397+4663d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | ||||||
| chr15:55735815
|
G | T | 112 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.397+4567C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735815 | ||||||
| chr15:55735819
|
A | G | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+4563T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735819 | ||||||
| chr15:55736029
|
C | T | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+4353G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736029 | ||||||
| chr15:55736110
|
C | T | 57 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+4272G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736110 | ||||||
| chr15:55736205
|
GA | G | 24 | a0001c0001t0025g0013a0001c0001t0025g0030a0001c0001t0056g0004others(21): Show | 24 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.397+4176delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736205 | ||||||
| chr15:55736210
|
G | C | 1 | a0001c0020t0058g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.397+4172C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736210 | ||||||
| chr15:55736341
|
C | G | 15 | a0001c0001t0002g0265a0001c0001t0002g0275a0001c0020t0058g0002others(12): Show | 15 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+4041G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736341 | ||||||
| chr15:55736364
|
C | T | 49 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+4018G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736364 | ||||||
| chr15:55736365
|
G | A | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+4017C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736365 | ||||||
| chr15:55736378
|
A | C | 112 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.397+4004T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736378 | ||||||
| chr15:55736380
|
C | CT | 16 | a0001c0001t0035g0001a0001c0001t0076g0133a0001c0012t0078g0113others(13): Show | 17 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+4001dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736380 | ||||||
| chr15:55736380
|
CTTTT | C | 57 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+3998_397+4001d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736380 | ||||||
| chr15:55736444
|
G | T | 13 | a0001c0020t0058g0002a0004c0005t0022g0039a0004c0005t0022g0041others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+3938C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736444 | ||||||
| chr15:55736503
|
T | C | 1 | a0001c0009t0113g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+3879A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736503 | ||||||
| chr15:55736659
|
C | A | 50 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+3723G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736659 | ||||||
| chr15:55736807
|
T | C | 1 | a0001c0001t0011g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.397+3575A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736807 | ||||||
| chr15:55737147
|
T | C | 55 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+3235A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737147 | ||||||
| chr15:55737180
|
T | C | 55 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+3202A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737180 | ||||||
| chr15:55737197
|
T | C | 58 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+3185A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737197 | ||||||
| chr15:55737276
|
G | A | 4 | a0001c0001t0030g0092a0001c0001t0072g0094a0002c0002t0021g0010others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+3106C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737276 | ||||||
| chr15:55737784
|
GCA | G | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+2596_397+2597d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737784 | ||||||
| chr15:55737898
|
G | GCTGCT | 89 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.397+2479_397+2483d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737898 | ||||||
| chr15:55737976
|
T | TTC | 23 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0200others(20): Show | 23 | HG00639.hp1 HG01243.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.397+2404_397+2405d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
T | TTCTC | 13 | a0001c0001t0001g0203a0001c0001t0034g0101a0001c0001t0036g0218others(10): Show | 13 | HG00323.hp1 HG01891.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+2402_397+2405d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
T | TTCTCTC | 5 | a0001c0001t0110g0217a0002c0002t0005g0108a0002c0002t0005g0216others(2): Show | 5 | HG02257.hp2 NA18943.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2400_397+2405d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
T | TTCTCTCT others(1): Show |
3 | a0001c0001t0023g0058a0002c0002t0020g0052a0003c0004t0031g0105 | 3 | HG02451.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.397+2398_397+2405d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
T | TTCTCTCT others(3): Show |
25 | a0001c0001t0011g0075a0001c0003t0003g0042a0001c0003t0003g0069others(22): Show | 25 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.397+2396_397+2405d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
T | TTCTCTCT others(5): Show |
5 | a0002c0002t0003g0076a0002c0002t0007g0070a0002c0002t0007g0085others(2): Show | 5 | HG01255.hp2 HG03209.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2394_397+2405d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
T | TTCTCTCT others(7): Show |
2 | a0001c0003t0003g0089a0002c0002t0003g0077 | 2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.397+2392_397+2405d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
T | TTCTCTCT others(9): Show |
1 | a0003c0004t0024g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.397+2390_397+2405d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737976
|
TTC | T | 3 | a0001c0001t0112g0128a0002c0002t0013g0033a0002c0002t0068g0032 | 3 | HG02559.hp2 HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.397+2404_397+2405d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | ||||||
| chr15:55737980
|
C | T | 11 | a0004c0005t0022g0039a0004c0005t0022g0041a0004c0005t0045g0040others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+2402G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737980 | ||||||
| chr15:55737996
|
C | A | 1 | a0001c0001t0035g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.397+2386G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737996 | ||||||
| chr15:55737998
|
C | A | 1 | a0001c0001t0035g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.397+2384G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737998 | ||||||
| chr15:55738000
|
C | A | 3 | a0001c0001t0035g0001a0001c0001t0076g0133a0002c0002t0010g0050 | 4 | HG01167.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2382G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738000 | ||||||
| chr15:55738000
|
CTCTA | C | 9 | a0001c0001t0015g0140a0001c0001t0025g0013a0002c0002t0013g0020others(6): Show | 9 | HG01361.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+2378_397+2381d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738000 | ||||||
| chr15:55738002
|
C | A | 7 | a0001c0001t0001g0149a0001c0001t0001g0224a0001c0001t0033g0098others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+2380G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738002
|
C | CTCTCTCT others(3): Show |
4 | a0001c0001t0011g0091a0001c0001t0019g0061a0002c0002t0003g0086others(1): Show | 4 | HG00323.hp2 HG02027.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2379_397+2380i others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738002
|
C | CTCTCTCT others(5): Show |
2 | a0002c0002t0015g0227a0003c0004t0055g0062 | 2 | HG02129.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.397+2379_397+2380i others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738002
|
C | CTCTCTCT others(7): Show |
1 | a0002c0002t0003g0087 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.397+2379_397+2380i others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738002
|
CTA | C | 17 | a0001c0001t0001g0151a0001c0001t0001g0226a0001c0001t0008g0152others(14): Show | 17 | HG00099.hp2 HG00733.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.397+2378_397+2379d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738002
|
CTATA | C | 12 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0012t0002g0279others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.397+2376_397+2379d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738002
|
CTATATA | C | 6 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+2374_397+2379d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738002
|
CTATATAT others(3): Show |
C | 1 | a0001c0007t0118g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+2370_397+2379d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | ||||||
| chr15:55738004
|
A | C | 143 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0130others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.397+2378T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738004 | ||||||
| chr15:55738004
|
A | T | 2 | a0002c0002t0013g0033a0002c0002t0068g0032 | 2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.397+2378T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738004 | ||||||
| chr15:55738006
|
A | C | 95 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0138others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.397+2376T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738006 | ||||||
| chr15:55738006
|
A | T | 15 | a0001c0001t0025g0013a0002c0002t0012g0018a0002c0002t0012g0028others(12): Show | 15 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+2376T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738006 | ||||||
| chr15:55738008
|
A | C | 54 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0226others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+2374T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738008 | ||||||
| chr15:55738008
|
A | T | 1 | a0002c0002t0012g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+2374T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738008 | ||||||
| chr15:55738010
|
A | C | 22 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(19): Show | 22 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.397+2372T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738010 | ||||||
| chr15:55738012
|
A | C | 8 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(5): Show | 8 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+2370T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738012 | ||||||
| chr15:55738015
|
T | C | 2 | a0001c0001t0035g0001a0001c0001t0076g0133 | 3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+2367A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738015 | ||||||
| chr15:55738017
|
T | C | 3 | a0001c0001t0035g0001a0001c0001t0076g0133a0001c0001t0094g0129 | 4 | HG03471.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2365A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738017 | ||||||
| chr15:55738017
|
TATATATA others(3): Show |
T | 3 | a0001c0007t0039g0231a0001c0007t0116g0109a0001c0007t0117g0110 | 3 | HG02109.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.397+2355_397+2364d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738017 | ||||||
| chr15:55738017
|
TATATATA others(7): Show |
T | 1 | a0008c0021t0102g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.397+2351_397+2364d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738017 | ||||||
| chr15:55738019
|
T | C | 11 | a0001c0001t0030g0092a0001c0001t0035g0001a0001c0001t0076g0133others(8): Show | 12 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+2363A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738019 | ||||||
| chr15:55738019
|
T | TAC | 5 | a0001c0001t0072g0094a0002c0002t0010g0048a0002c0002t0010g0049others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2362_397+2363i others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738019 | ||||||
| chr15:55738021
|
T | C | 38 | a0001c0001t0001g0144a0001c0001t0001g0203a0001c0001t0016g0201others(35): Show | 39 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.397+2361A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738021 | ||||||
| chr15:55738021
|
TATATAC | T | 25 | a0001c0001t0002g0238a0001c0001t0002g0248a0001c0001t0002g0249others(22): Show | 25 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.397+2355_397+2360d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738021 | ||||||
| chr15:55738023
|
T | C | 149 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(146): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.397+2359A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738023 | ||||||
| chr15:55738023
|
T | TACAC | 3 | a0001c0001t0033g0103a0001c0001t0034g0102a0002c0002t0074g0099 | 3 | HG02965.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.397+2358_397+2359i others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738023 | ||||||
| chr15:55738023
|
TATAC | T | 12 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(9): Show | 12 | HG01167.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+2355_397+2358d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738023 | ||||||
| chr15:55738025
|
T | C | 174 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.397+2357A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738025 | ||||||
| chr15:55738025
|
T | TATAC | 3 | a0002c0002t0005g0118a0002c0002t0005g0119a0002c0002t0005g0120 | 3 | NA18964.hp1 NA18981.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.397+2356_397+2357i others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738025 | ||||||
| chr15:55738025
|
TAC | T | 3 | a0001c0001t0023g0051a0001c0001t0106g0229a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.397+2355_397+2356d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738025 | ||||||
| chr15:55738027
|
C | T | 5 | a0001c0001t0002g0270a0001c0001t0002g0274a0001c0001t0004g0281others(2): Show | 5 | HG01943.hp2 HG01993.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2355G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738027 | ||||||
| chr15:55738029
|
C | T | 3 | a0001c0001t0023g0051a0001c0001t0106g0229a0001c0001t0111g0228 | 3 | HG02647.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.397+2353G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738029 | ||||||
| chr15:55738071
|
A | AAT | 32 | a0001c0001t0001g0131a0001c0001t0017g0122a0001c0001t0017g0123others(29): Show | 32 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.397+2309_397+2310d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATAT | 120 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0130others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.397+2307_397+2310d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATAT | 22 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0001t0001g0224others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.397+2305_397+2310d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(1): Show |
15 | a0001c0001t0002g0275a0001c0001t0006g0137a0001c0001t0011g0091others(12): Show | 15 | HG00323.hp2 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.397+2303_397+2310d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(3): Show |
16 | a0001c0001t0001g0115a0001c0001t0002g0246a0001c0001t0002g0265others(13): Show | 16 | HG01256.hp2 HG01258.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.397+2301_397+2310d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(5): Show |
4 | a0001c0001t0001g0134a0001c0001t0004g0264a0001c0001t0035g0001others(1): Show | 5 | HG00733.hp1 HG02027.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2299_397+2310d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(7): Show |
1 | a0001c0001t0076g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.397+2297_397+2310d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(9): Show |
2 | a0001c0001t0004g0263a0001c0001t0042g0262 | 2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.397+2295_397+2310d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(11): Show |
5 | a0001c0001t0002g0245a0001c0001t0002g0261a0001c0001t0004g0258others(2): Show | 5 | HG03688.hp2 HG04115.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2293_397+2310d others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(13): Show |
7 | a0001c0001t0001g0206a0001c0001t0002g0257a0001c0001t0004g0256others(4): Show | 7 | HG02257.hp1 HG02273.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+2291_397+2310d others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(15): Show |
3 | a0001c0001t0004g0255a0001c0001t0109g0232a0012c0017t0002g0254 | 3 | HG00140.hp1 HG01517.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.397+2289_397+2310d others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(17): Show |
5 | a0001c0001t0002g0238a0001c0001t0004g0243a0001c0001t0004g0244others(2): Show | 5 | HG00639.hp2 HG01515.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2310_397+2311i others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(19): Show |
2 | a0001c0001t0002g0242a0001c0001t0042g0280 | 2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.397+2310_397+2311i others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(21): Show |
5 | a0001c0001t0002g0241a0001c0001t0002g0249a0001c0001t0002g0251others(2): Show | 5 | HG01071.hp1 HG01106.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2310_397+2311i others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(23): Show |
2 | a0001c0001t0002g0240a0001c0001t0002g0248 | 2 | HG00741.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.397+2310_397+2311i others(32): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738071
|
A | AATATATA others(27): Show |
1 | a0001c0001t0004g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.397+2310_397+2311i others(36): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | ||||||
| chr15:55738195
|
TCAC | T | 7 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(4): Show | 7 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+2184_397+2186d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738195 | ||||||
| chr15:55738245
|
G | A | 50 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+2137C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738245 | ||||||
| chr15:55738345
|
G | A | 52 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(49): Show | 52 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.397+2037C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738345 | ||||||
| chr15:55738371
|
A | G | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+2011T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738371 | ||||||
| chr15:55738372
|
A | G | 3 | a0002c0002t0003g0043a0002c0002t0003g0088a0002c0002t0007g0044 | 3 | HG00438.hp2 HG02027.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.397+2010T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738372 | ||||||
| chr15:55738503
|
AAAGAT | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0206a0001c0001t0008g0207 | 3 | NA18948.hp2 NA18980.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.397+1874_397+1878d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738503 | ||||||
| chr15:55738539
|
C | T | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+1843G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738539 | ||||||
| chr15:55738546
|
T | G | 5 | a0001c0008t0038g0209a0001c0008t0038g0210a0001c0008t0083g0121others(2): Show | 5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+1836A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738546 | ||||||
| chr15:55738558
|
T | C | 54 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(51): Show | 54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+1824A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738558 | ||||||
| chr15:55738648
|
T | G | 57 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+1734A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738648 | ||||||
| chr15:55738731
|
A | C | 1 | a0001c0003t0003g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.397+1651T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738731 | ||||||
| chr15:55738774
|
A | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.397+1608T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738774 | ||||||
| chr15:55738801
|
GAGGA | G | 3 | a0001c0001t0056g0004a0001c0001t0057g0006a0001c0001t0059g0005 | 3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+1577_397+1580d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738801 | ||||||
| chr15:55738828
|
A | G | 218 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0115others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.397+1554T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738828 | ||||||
| chr15:55738884
|
A | G | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1498T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738884 | ||||||
| chr15:55738887
|
CAGAGGAA others(4): Show |
C | 8 | a0001c0001t0017g0122a0001c0001t0017g0123a0001c0001t0092g0127others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.397+1484_397+1494d others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738887 | ||||||
| chr15:55738888
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1494T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738888 | ||||||
| chr15:55738910
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1472T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738910 | ||||||
| chr15:55738917
|
G | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1465C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738917 | ||||||
| chr15:55738924
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1458T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738924 | ||||||
| chr15:55738926
|
G | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1456C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738926 | ||||||
| chr15:55738927
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1455T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738927 | ||||||
| chr15:55738928
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1454T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738928 | ||||||
| chr15:55738931
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1451T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738931 | ||||||
| chr15:55738932
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1450T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738932 | ||||||
| chr15:55738935
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1447T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738935 | ||||||
| chr15:55738939
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1443T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738939 | ||||||
| chr15:55738940
|
G | T | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1442C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738940 | ||||||
| chr15:55738943
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1439T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738943 | ||||||
| chr15:55738947
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1435T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738947 | ||||||
| chr15:55738949
|
A | C | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1433T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738949 | ||||||
| chr15:55738950
|
G | T | 1 | a0001c0001t0056g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1432C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738950 | ||||||
| chr15:55738963
|
G | A | 1 | a0001c0001t0008g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.397+1419C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738963 | ||||||
| chr15:55739009
|
G | A | 2 | a0001c0001t0001g0224a0001c0003t0005g0225 | 2 | NA18994.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.397+1373C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739009 | ||||||
| chr15:55739042
|
C | T | 52 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(49): Show | 52 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.397+1340G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739042 | ||||||
| chr15:55739171
|
A | C | 1 | a0001c0008t0083g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.397+1211T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739171 | ||||||
| chr15:55739263
|
A | AT | 56 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0016g0116others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.397+1118dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739263 | ||||||
| chr15:55739263
|
ATT | A | 55 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+1117_397+1118d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739263 | ||||||
| chr15:55739418
|
G | C | 1 | a0001c0003t0018g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.397+964C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739418 | ||||||
| chr15:55739473
|
G | A | 106 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.397+909C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739473 | ||||||
| chr15:55739606
|
A | G | 1 | a0003c0004t0031g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+776T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739606 | ||||||
| chr15:55739724
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.397+658A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739724 | ||||||
| chr15:55739880
|
G | A | 1 | a0001c0001t0011g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.397+502C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739880 | ||||||
| chr15:55739890
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.397+492T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739890 | ||||||
| chr15:55739901
|
A | G | 109 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.397+481T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739901 | ||||||
| chr15:55740068
|
T | G | 2 | a0001c0020t0058g0002a0011c0019t0051g0003 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+314A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740068 | ||||||
| chr15:55740213
|
T | C | 54 | a0001c0001t0011g0075a0001c0001t0011g0091a0001c0001t0019g0061others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.397+169A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740213 | ||||||
| chr15:55740242
|
T | A | 2 | a0001c0001t0106g0229a0001c0001t0111g0228 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+140A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740242 | ||||||
| chr15:55740321
|
G | A | 46 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.397+61C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740321 | ||||||
| chr15:55740777
|
G | A | 104 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(101): Show | 104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.95-93C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55740777 | ||||||
| chr15:55741398
|
G | T | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.95-714C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741398 | ||||||
| chr15:55741399
|
G | T | 2 | a0001c0012t0078g0113a0001c0012t0080g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.95-715C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741399 | ||||||
| chr15:55741649
|
G | A | 53 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(50): Show | 53 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.95-965C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741649 | ||||||
| chr15:55741771
|
C | T | 2 | a0001c0020t0058g0002a0011c0019t0051g0003 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.94+1067G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741771 | ||||||
| chr15:55741866
|
C | A | 3 | a0001c0001t0004g0281a0001c0001t0004g0282a0001c0001t0042g0280 | 3 | HG01361.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.94+972G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741866 | ||||||
| chr15:55741906
|
C | T | 2 | a0003c0004t0032g0095a0003c0004t0032g0096 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.94+932G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741906 | ||||||
| chr15:55741909
|
T | C | 54 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(51): Show | 54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.94+929A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741909 | ||||||
| chr15:55742333
|
C | T | 4 | a0001c0007t0116g0109a0001c0007t0117g0110a0001c0007t0118g0111others(1): Show | 4 | HG02109.hp2 HG02615.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+505G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742333 | ||||||
| chr15:55742397
|
C | A | 1 | a0001c0001t0109g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94+441G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742397 | ||||||
| chr15:55742491
|
C | T | 1 | a0002c0002t0005g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.94+347G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742491 | ||||||
| chr15:55742672
|
G | A | 2 | a0001c0009t0113g0233a0010c0014t0079g0234 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94+166C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742672 | ||||||
| chr15:55742680
|
G | A | 46 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.94+158C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742680 | ||||||
| chr15:55742713
|
G | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | NA18981.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.94+125C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742713 | ||||||
| chr15:55742787
|
G | T | 1 | a0001c0001t0002g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.94+51C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742787 | ||||||
| chr15:55742812
|
G | A | 46 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0241others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.94+26C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742812 |