| geneid | 5800 |
|---|---|
| ensemblid | ENSG00000151490.15 |
| hgncid | 9678 |
| symbol | PTPRO |
| name | protein tyrosine phosphatase receptor type O |
| refseq_nuc | NM_030667.3 |
| refseq_prot | NP_109592.1 |
| ensembl_nuc | ENST00000281171.9 |
| ensembl_prot | ENSP00000281171.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 15322508 |
| end | 15598331 |
| strand | + |
| ver | v1.2 |
| region | chr12:15322508-15598331 |
| region5000 | chr12:15317508-15603331 |
| regionname0 | PTPRO_chr12_15322508_15598331 |
| regionname5000 | PTPRO_chr12_15317508_15603331 |
| 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 | 1216 | 162 | 64 | 24 | 52 | 5 | 15 | 36 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0002 | 0/0 | 1216 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0003 | 0/0 | 1216 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| 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 | 1/0 | 3651 | 62 | 15 | 10 | 26 | 3 | 7 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0002 | 0/1 | 3651 | 50 | 34 | 6 | 5 | 0 | 4 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0003 | 0/0 | 3651 | 19 | 5 | 2 | 9 | 1 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0004 | 0/0 | 3651 | 14 | 4 | 4 | 4 | 0 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0005 | 0/0 | 3651 | 5 | 4 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0006 | 0/0 | 3651 | 4 | 0 | 0 | 4 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0007 | 0/0 | 3651 | 3 | 0 | 0 | 2 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0008 | 0/0 | 3651 | 2 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0009 | 0/0 | 3651 | 2 | 0 | 0 | 2 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0010 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0011 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| c0012 | 0/0 | 3651 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| 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 | 0/1 | 2478 | 92 | 12 | 16 | 44 | 6 | 13 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0002 | 0/0 | 2478 | 15 | 14 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0003 | 1/0 | 2478 | 14 | 11 | 2 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0004 | 0/0 | 2478 | 10 | 6 | 0 | 4 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0005 | 0/0 | 2478 | 7 | 5 | 2 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0006 | 0/0 | 2481 | 6 | 4 | 2 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0007 | 0/0 | 2478 | 5 | 5 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0008 | 0/0 | 2481 | 3 | 3 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0009 | 0/0 | 2478 | 3 | 0 | 0 | 3 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0010 | 0/0 | 2478 | 2 | 0 | 0 | 0 | 0 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0011 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0012 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0013 | 0/0 | 2478 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0014 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0015 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0016 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| t0017 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| 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 | 1/0 | 3651 | 62 | 15 | 10 | 26 | 3 | 7 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002 | 0/1 | 3651 | 50 | 34 | 6 | 5 | 0 | 4 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0003 | 0/0 | 3651 | 19 | 5 | 2 | 9 | 1 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0004 | 0/0 | 3651 | 14 | 4 | 4 | 4 | 0 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0005 | 0/0 | 3651 | 5 | 4 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0006 | 0/0 | 3651 | 4 | 0 | 0 | 4 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0007 | 0/0 | 3651 | 3 | 0 | 0 | 2 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0008 | 0/0 | 3651 | 2 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0009 | 0/0 | 3651 | 2 | 0 | 0 | 2 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0012 | 0/0 | 3651 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0002c0011 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0003c0010 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6128 | 42 | 4 | 7 | 23 | 3 | 5 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0002 | 0/0 | 6128 | 3 | 3 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0003 | 1/0 | 6128 | 3 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0004 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0005 | 0/0 | 6128 | 2 | 1 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0006 | 0/0 | 6131 | 2 | 1 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0007 | 0/0 | 6128 | 2 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0008 | 0/0 | 6131 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0009 | 0/0 | 6128 | 3 | 0 | 0 | 3 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0010 | 0/0 | 6128 | 2 | 0 | 0 | 0 | 0 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0001t0014 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0001 | 0/1 | 6128 | 16 | 3 | 3 | 5 | 0 | 4 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0002 | 0/0 | 6128 | 9 | 8 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0003 | 0/0 | 6128 | 11 | 9 | 2 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0004 | 0/0 | 6128 | 3 | 3 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0005 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0006 | 0/0 | 6131 | 3 | 3 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0007 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0008 | 0/0 | 6131 | 2 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0011 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0012 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0015 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0002t0016 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0003t0001 | 0/0 | 6128 | 16 | 3 | 2 | 8 | 1 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0003t0007 | 0/0 | 6128 | 2 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0003t0017 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0004t0001 | 0/0 | 6128 | 12 | 2 | 4 | 4 | 0 | 2 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0004t0002 | 0/0 | 6128 | 2 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0005t0002 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0005t0005 | 0/0 | 6128 | 4 | 3 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0006t0004 | 0/0 | 6128 | 4 | 0 | 0 | 4 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0007t0001 | 0/0 | 6128 | 3 | 0 | 0 | 2 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0008t0004 | 0/0 | 6128 | 2 | 2 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0009t0001 | 0/0 | 6128 | 2 | 0 | 0 | 2 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0001c0012t0006 | 0/0 | 6131 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0002c0011t0001 | 0/0 | 6128 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| a0003c0010t0013 | 0/0 | 6128 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | copy fasta | chr12 | 15317508 | 15603331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0003g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0009g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0002t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0003t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0004t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0005t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0005t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0005t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0005t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0005t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0006t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0006t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0006t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0006t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0007t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0007t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0008t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0008t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0009t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0009t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0001c0012t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0002c0011t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| a0003c0010t0013g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0007 | t0001 | g0053 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00423 | hp2 | a0001 | c0006 | t0004 | g0114 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00597 | hp1 | a0001 | c0006 | t0004 | g0045 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00673 | hp2 | a0001 | c0001 | t0009 | g0048 | EAS | CHS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00733 | hp1 | a0001 | c0012 | t0006 | g0070 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00733 | hp2 | a0001 | c0005 | t0005 | g0096 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0129 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0033 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0055 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0147 | AMR | PUR | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0089 | AMR | CLM | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0068 | AMR | CLM | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01516 | hp1 | a0002 | c0011 | t0001 | g0092 | EUR | IBS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0145 | EUR | IBS | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0075 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0036 | AMR | PEL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PEL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01981 | hp2 | a0001 | c0001 | t0014 | g0001 | AMR | PEL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | KHV | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02132 | hp2 | a0001 | c0006 | t0004 | g0123 | EAS | KHV | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0085 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02257 | hp2 | a0001 | c0005 | t0005 | g0108 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0143 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02258 | hp2 | a0001 | c0003 | t0007 | g0164 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02451 | hp1 | a0001 | c0002 | t0006 | g0058 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0079 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02630 | hp1 | a0001 | c0002 | t0008 | g0027 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0066 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02683 | hp1 | a0003 | c0010 | t0013 | g0054 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02717 | hp1 | a0001 | c0002 | t0012 | g0084 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0057 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02809 | hp1 | a0001 | c0005 | t0005 | g0097 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0099 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02922 | hp2 | a0001 | c0005 | t0002 | g0109 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0083 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0162 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03098 | hp2 | a0001 | c0002 | t0015 | g0095 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0127 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0116 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0052 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03225 | hp2 | a0001 | c0004 | t0002 | g0161 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0163 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0142 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0022 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03492 | hp1 | a0001 | c0001 | t0010 | g0023 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0094 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0080 | AFR | GWD | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03579 | hp2 | a0001 | c0003 | t0007 | g0081 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0157 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | STU | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0159 | SAS | STU | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | BEB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0051 | SAS | BEB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18747 | hp2 | a0001 | c0001 | t0009 | g0046 | EAS | CHB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18946 | hp1 | a0001 | c0009 | t0001 | g0153 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18960 | hp2 | a0001 | c0006 | t0004 | g0152 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18961 | hp2 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18986 | hp1 | a0001 | c0009 | t0001 | g0154 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19003 | hp1 | a0001 | c0003 | t0017 | g0107 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19030 | hp1 | a0001 | c0008 | t0004 | g0071 | AFR | LWK | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0072 | AFR | LWK | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19066 | hp2 | a0001 | c0007 | t0001 | g0112 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0076 | AFR | YRI | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | YRI | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | ASW | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ASW | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA20805 | hp1 | a0001 | c0007 | t0001 | g0118 | EUR | TSI | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02109 | hp1 | a0001 | c0002 | t0011 | g0082 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02109 | hp2 | a0001 | c0002 | t0006 | g0059 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03471 | hp1 | a0001 | c0002 | t0016 | g0061 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0133 | AFR | MSL | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG06807 | hp1 | a0001 | c0008 | t0004 | g0040 | AFR | USA | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | USA | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | LWK | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| NA21309 | hp2 | a0001 | c0005 | t0005 | g0098 | AFR | LWK | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0141 | REF | REF | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0158 | REF | REF | PTPRO_chr12_15317508_15603331 | PTPRO | chr12 | 15317508 | 15603331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15501802
|
G | A | 1 | a0003 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.844G>A | p.Gly282Ser | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/27 | 1063/6128 | 844/3651 | 282/1216 | chr12 | 15501802 | ||
| chr12:15508630
|
G | A | 1 | a0002 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1327G>A | p.Val443Ile | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/27 | 1546/6128 | 1327/3651 | 443/1216 | chr12 | 15508630 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15516803
|
T | C | 2 | a0001c0004a0001c0007 | 17 | HG00423.hp1 HG01169.hp1 HG01243.hp1 others(14): Show |
synonymous_variant | LOW | c.1626T>C | p.Gly542Gly | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/27 | 1845/6128 | 1626/3651 | 542/1216 | chr12 | 15516803 | ||
| chr12:15526186
|
C | A | 6 | a0001c0002a0001c0004a0001c0005others(3): Show | 74 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(71): Show |
synonymous_variant | LOW | c.2088C>A | p.Gly696Gly | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/27 | 2307/6128 | 2088/3651 | 696/1216 | chr12 | 15526186 | ||
| chr12:15526198
|
C | T | 1 | a0001c0005 | 5 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.2100C>T | p.Asn700Asn | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/27 | 2319/6128 | 2100/3651 | 700/1216 | chr12 | 15526198 | ||
| chr12:15546660
|
T | C | 1 | a0001c0008 | 2 | HG06807.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.2256T>C | p.Phe752Phe | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/27 | 2475/6128 | 2256/3651 | 752/1216 | chr12 | 15546660 | ||
| chr12:15580735
|
G | A | 2 | a0001c0003a0001c0009 | 21 | HG00597.hp2 HG00621.hp2 HG01261.hp1 others(18): Show |
synonymous_variant | LOW | c.3036G>A | p.Gly1012Gly | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/27 | 3255/6128 | 3036/3651 | 1012/1216 | chr12 | 15580735 | ||
| chr12:15581768
|
C | T | 1 | a0001c0012 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.3222C>T | p.Asp1074Asp | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/27 | 3441/6128 | 3222/3651 | 1074/1216 | chr12 | 15581768 | ||
| chr12:15586902
|
C | T | 1 | a0001c0006 | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
synonymous_variant | LOW | c.3261C>T | p.Asp1087Asp | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/27 | 3480/6128 | 3261/3651 | 1087/1216 | chr12 | 15586902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15322542
|
T | C | 5 | a0001c0001t0007a0001c0002t0007a0001c0002t0011others(2): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-185T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/27 | 185 | chr12 | 15322542 | |||||
| chr12:15595051
|
C | T | 1 | a0001c0003t0017 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 26/27 | 10 | chr12 | 15595051 | |||||
| chr12:15596138
|
G | T | 1 | a0001c0001t0009 | 3 | HG00673.hp2 HG02132.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*65G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1097 | chr12 | 15596138 | |||||
| chr12:15596144
|
C | G | 1 | a0001c0002t0016 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1103 | chr12 | 15596144 | |||||
| chr12:15596514
|
C | G | 5 | a0001c0001t0002a0001c0002t0002a0001c0002t0012others(2): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*441C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1473 | chr12 | 15596514 | |||||
| chr12:15596667
|
G | A | 1 | a0003c0010t0013 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*594G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1626 | chr12 | 15596667 | |||||
| chr12:15596797
|
G | T | 5 | a0001c0001t0002a0001c0002t0002a0001c0002t0012others(2): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*724G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1756 | chr12 | 15596797 | |||||
| chr12:15596822
|
C | CTAA | 5 | a0001c0001t0006a0001c0001t0008a0001c0002t0006others(2): Show | 9 | HG00733.hp1 HG01261.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*751_*753dupAAT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1786 | INFO_REALIGN_3_PRIME | chr12 | 15596822 | ||||
| chr12:15596958
|
A | G | 4 | a0001c0001t0005a0001c0002t0005a0001c0002t0015others(1): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*885A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1917 | chr12 | 15596958 | |||||
| chr12:15597005
|
G | A | 1 | a0001c0002t0015 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 1964 | chr12 | 15597005 | |||||
| chr12:15597087
|
T | C | 5 | a0001c0001t0002a0001c0002t0002a0001c0002t0012others(2): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1014T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 2046 | chr12 | 15597087 | |||||
| chr12:15597228
|
C | T | 1 | a0001c0001t0014 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1155C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 2187 | chr12 | 15597228 | |||||
| chr12:15597457
|
G | A | 15 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(12): Show | 105 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1384G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 2416 | chr12 | 15597457 | |||||
| chr12:15597737
|
G | A | 1 | a0001c0002t0016 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1664G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 2696 | chr12 | 15597737 | |||||
| chr12:15597770
|
C | T | 1 | a0001c0001t0010 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1697C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 2729 | chr12 | 15597770 | |||||
| chr12:15597829
|
G | A | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(32): Show | 150 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1756G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 2788 | chr12 | 15597829 | |||||
| chr12:15598014
|
T | G | 1 | a0001c0002t0016 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1941T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 2973 | chr12 | 15598014 | |||||
| chr12:15598181
|
G | C | 3 | a0001c0001t0006a0001c0002t0006a0001c0012t0006 | 6 | HG00733.hp1 HG01261.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2108G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 3140 | chr12 | 15598181 | |||||
| chr12:15598250
|
G | A | 1 | a0001c0002t0016 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 27/27 | 3209 | chr12 | 15598250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15323084
|
C | T | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+283C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15323084 | ||||||
| chr12:15323135
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+334T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15323135 | ||||||
| chr12:15323139
|
A | G | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+338A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15323139 | ||||||
| chr12:15323951
|
C | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+1150C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15323951 | ||||||
| chr12:15324749
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 88 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.75+1948T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15324749 | ||||||
| chr12:15325394
|
A | G | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+2593A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15325394 | ||||||
| chr12:15325631
|
A | G | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+2830A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15325631 | ||||||
| chr12:15325648
|
C | T | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+2847C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15325648 | ||||||
| chr12:15325846
|
T | C | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.75+3045T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15325846 | ||||||
| chr12:15326298
|
T | TA | 5 | a0001c0001t0001g0029a0001c0001t0003g0030a0001c0002t0001g0032others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+3500dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15326298 | |||||
| chr12:15326898
|
T | C | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+4097T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15326898 | ||||||
| chr12:15327240
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+4439C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15327240 | ||||||
| chr12:15327241
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.75+4440C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15327241 | ||||||
| chr12:15327430
|
C | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.75+4629C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15327430 | ||||||
| chr12:15327685
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+4884G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15327685 | ||||||
| chr12:15327942
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+5141C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15327942 | ||||||
| chr12:15327974
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+5173T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15327974 | ||||||
| chr12:15328113
|
C | CA | 9 | a0001c0001t0007g0083a0001c0002t0001g0035a0001c0002t0004g0163others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+5327dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15328113 | |||||
| chr12:15328291
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+5490T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15328291 | ||||||
| chr12:15328324
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.75+5523G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15328324 | ||||||
| chr12:15328392
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+5591T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15328392 | ||||||
| chr12:15328754
|
CTT | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0003t0001g0036 | 3 | HG01934.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.75+5955_75+5956del others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15328754 | |||||
| chr12:15328812
|
T | G | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+6011T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15328812 | ||||||
| chr12:15328869
|
G | A | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+6068G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15328869 | ||||||
| chr12:15329094
|
C | T | 2 | a0001c0004t0001g0024a0001c0004t0001g0025 | 2 | NA18989.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.75+6293C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15329094 | ||||||
| chr12:15329592
|
C | G | 1 | a0001c0002t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.75+6791C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15329592 | ||||||
| chr12:15329660
|
T | C | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.75+6859T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15329660 | ||||||
| chr12:15329896
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.75+7095G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15329896 | ||||||
| chr12:15330004
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+7203G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15330004 | ||||||
| chr12:15330093
|
T | C | 1 | a0001c0003t0001g0038 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.75+7292T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15330093 | ||||||
| chr12:15330096
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.75+7295C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15330096 | ||||||
| chr12:15330683
|
T | C | 1 | a0001c0003t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.75+7882T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15330683 | ||||||
| chr12:15330727
|
A | G | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+7926A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15330727 | ||||||
| chr12:15330836
|
G | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.75+8035G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15330836 | ||||||
| chr12:15331104
|
G | T | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+8303G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15331104 | ||||||
| chr12:15331138
|
A | G | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0163others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+8337A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15331138 | ||||||
| chr12:15331339
|
C | T | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+8538C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15331339 | ||||||
| chr12:15331744
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.75+8943T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15331744 | ||||||
| chr12:15331948
|
G | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.75+9147G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15331948 | ||||||
| chr12:15331962
|
C | CT | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+9181dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15331962 | |||||
| chr12:15331962
|
CT | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0090others(3): Show | 6 | HG01167.hp2 HG01934.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+9181delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15331962 | |||||
| chr12:15332212
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG01169.hp1 HG02300.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+9411G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15332212 | ||||||
| chr12:15332829
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+10028C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15332829 | ||||||
| chr12:15333231
|
T | G | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0163others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+10430T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15333231 | ||||||
| chr12:15333274
|
T | C | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0163others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+10473T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15333274 | ||||||
| chr12:15333413
|
A | G | 1 | a0001c0004t0002g0127 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.75+10612A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15333413 | ||||||
| chr12:15333546
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.75+10745T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15333546 | ||||||
| chr12:15333616
|
C | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+10815C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15333616 | ||||||
| chr12:15333653
|
G | T | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.75+10852G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15333653 | ||||||
| chr12:15333903
|
G | C | 1 | a0002c0011t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.75+11102G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15333903 | ||||||
| chr12:15334087
|
T | C | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+11286T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15334087 | ||||||
| chr12:15335215
|
A | G | 23 | a0001c0001t0001g0088a0001c0001t0001g0110a0001c0001t0001g0111others(20): Show | 23 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.75+12414A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15335215 | ||||||
| chr12:15335293
|
A | C | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+12492A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15335293 | ||||||
| chr12:15335343
|
T | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+12542T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15335343 | ||||||
| chr12:15335627
|
A | G | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0163others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+12826A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15335627 | ||||||
| chr12:15335827
|
A | G | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+13026A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15335827 | ||||||
| chr12:15336231
|
T | TA | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+13442dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15336231 | |||||
| chr12:15336372
|
G | A | 5 | a0001c0001t0003g0030a0001c0002t0001g0032a0001c0002t0002g0031others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+13571G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15336372 | ||||||
| chr12:15336539
|
G | C | 9 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0009g0046others(6): Show | 9 | HG00597.hp1 HG00673.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+13738G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15336539 | ||||||
| chr12:15336802
|
A | C | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+14001A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15336802 | ||||||
| chr12:15336823
|
T | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+14022T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15336823 | ||||||
| chr12:15337344
|
A | G | 1 | a0001c0012t0006g0070 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.75+14543A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15337344 | ||||||
| chr12:15337845
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.75+15044T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15337845 | ||||||
| chr12:15337932
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+15131C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15337932 | ||||||
| chr12:15338046
|
G | A | 1 | a0001c0002t0002g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.75+15245G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338046 | ||||||
| chr12:15338186
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.75+15385T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338186 | ||||||
| chr12:15338207
|
G | A | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+15406G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338207 | ||||||
| chr12:15338226
|
T | G | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+15425T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338226 | ||||||
| chr12:15338230
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.75+15429G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338230 | ||||||
| chr12:15338454
|
A | G | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.75+15653A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338454 | ||||||
| chr12:15338801
|
C | T | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75+16000C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338801 | ||||||
| chr12:15338889
|
T | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+16088T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15338889 | ||||||
| chr12:15339301
|
A | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+16500A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15339301 | ||||||
| chr12:15339542
|
T | A | 2 | a0001c0002t0001g0013a0001c0003t0001g0012 | 2 | NA18949.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.75+16741T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15339542 | ||||||
| chr12:15339651
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+16850C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15339651 | ||||||
| chr12:15339818
|
T | G | 8 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0002t0004g0056others(5): Show | 8 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+17017T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15339818 | ||||||
| chr12:15339897
|
T | C | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.75+17096T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15339897 | ||||||
| chr12:15340298
|
G | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0078others(21): Show | 24 | HG00733.hp1 HG01109.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.75+17497G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15340298 | ||||||
| chr12:15340398
|
G | C | 1 | a0001c0001t0003g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.75+17597G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15340398 | ||||||
| chr12:15340454
|
A | T | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+17653A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15340454 | ||||||
| chr12:15340744
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+17943C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15340744 | ||||||
| chr12:15340859
|
A | T | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+18058A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15340859 | ||||||
| chr12:15341002
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.75+18201A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341002 | ||||||
| chr12:15341469
|
T | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+18668T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341469 | ||||||
| chr12:15341493
|
G | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0003t0001g0036 | 3 | HG01934.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.75+18692G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341493 | ||||||
| chr12:15341677
|
G | A | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.75+18876G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341677 | ||||||
| chr12:15341686
|
G | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+18885G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341686 | ||||||
| chr12:15341702
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+18901A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341702 | ||||||
| chr12:15341741
|
T | C | 1 | a0001c0002t0003g0057 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.75+18940T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341741 | ||||||
| chr12:15341774
|
C | T | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0163others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+18973C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15341774 | ||||||
| chr12:15342038
|
G | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.75+19237G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15342038 | ||||||
| chr12:15342310
|
ATTG | A | 3 | a0001c0001t0010g0022a0001c0001t0010g0023a0001c0002t0001g0008 | 3 | HG03491.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.75+19515_75+19517d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15342310 | |||||
| chr12:15342536
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.75+19735G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15342536 | ||||||
| chr12:15342832
|
T | C | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+20031T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15342832 | ||||||
| chr12:15343371
|
AC | A | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+20572delC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15343371 | |||||
| chr12:15343673
|
C | T | 14 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0003g0030others(11): Show | 14 | HG00597.hp1 HG00673.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+20872C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15343673 | ||||||
| chr12:15343717
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.75+20916A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15343717 | ||||||
| chr12:15343787
|
G | A | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+20986G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15343787 | ||||||
| chr12:15343800
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+20999G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15343800 | ||||||
| chr12:15344045
|
C | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0078others(21): Show | 24 | HG00733.hp1 HG01109.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.75+21244C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344045 | ||||||
| chr12:15344101
|
C | G | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+21300C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344101 | ||||||
| chr12:15344202
|
A | C | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+21401A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344202 | ||||||
| chr12:15344436
|
A | T | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21635A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344436 | ||||||
| chr12:15344618
|
T | A | 1 | a0001c0001t0001g0110 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.75+21817T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344618 | ||||||
| chr12:15344639
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+21838G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344639 | ||||||
| chr12:15344702
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.75+21901G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344702 | ||||||
| chr12:15344884
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.75+22083G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344884 | ||||||
| chr12:15344971
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+22170C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15344971 | ||||||
| chr12:15345008
|
C | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+22207C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15345008 | ||||||
| chr12:15345212
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+22411A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15345212 | ||||||
| chr12:15345265
|
GTATCAC | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+22467_75+22472d others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15345265 | |||||
| chr12:15345532
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+22731T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15345532 | ||||||
| chr12:15345741
|
T | C | 1 | a0001c0002t0002g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.75+22940T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15345741 | ||||||
| chr12:15345972
|
C | A | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+23171C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15345972 | ||||||
| chr12:15346031
|
A | C | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.75+23230A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15346031 | ||||||
| chr12:15346177
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+23376C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15346177 | ||||||
| chr12:15346679
|
T | A | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+23878T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15346679 | ||||||
| chr12:15346702
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(14): Show | 17 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.75+23901G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15346702 | ||||||
| chr12:15346947
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.75+24146T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15346947 | ||||||
| chr12:15347064
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.75+24263G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347064 | ||||||
| chr12:15347102
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+24301C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347102 | ||||||
| chr12:15347171
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+24370T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347171 | ||||||
| chr12:15347212
|
A | G | 2 | a0001c0001t0001g0156a0001c0002t0001g0155 | 2 | HG02683.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.75+24411A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347212 | ||||||
| chr12:15347242
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+24441T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347242 | ||||||
| chr12:15347249
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+24448G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347249 | ||||||
| chr12:15347435
|
T | A | 2 | a0001c0002t0006g0058a0001c0002t0006g0059 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.75+24634T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347435 | ||||||
| chr12:15347519
|
C | T | 23 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0078others(20): Show | 23 | HG00733.hp1 HG01109.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.75+24718C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15347519 | ||||||
| chr12:15348336
|
G | A | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75+25535G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348336 | ||||||
| chr12:15348421
|
C | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+25620C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348421 | ||||||
| chr12:15348430
|
A | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+25629A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348430 | ||||||
| chr12:15348494
|
G | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+25693G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348494 | ||||||
| chr12:15348759
|
C | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+25958C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348759 | ||||||
| chr12:15348783
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+25982C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348783 | ||||||
| chr12:15348785
|
C | CA | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(26): Show | 29 | HG00735.hp1 HG00735.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.75+25999dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15348785 | |||||
| chr12:15348926
|
T | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+26125T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348926 | ||||||
| chr12:15348977
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+26176A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15348977 | ||||||
| chr12:15349127
|
A | G | 3 | a0001c0006t0004g0152a0001c0009t0001g0153a0001c0009t0001g0154 | 3 | NA18946.hp1 NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.75+26326A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15349127 | ||||||
| chr12:15349155
|
T | C | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+26354T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15349155 | ||||||
| chr12:15349172
|
T | A | 5 | a0001c0001t0003g0030a0001c0002t0001g0032a0001c0002t0002g0031others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+26371T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15349172 | ||||||
| chr12:15349176
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.75+26375A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15349176 | ||||||
| chr12:15349470
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+26669A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15349470 | ||||||
| chr12:15349743
|
A | G | 1 | a0001c0005t0002g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+26942A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15349743 | ||||||
| chr12:15350173
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.75+27372T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15350173 | ||||||
| chr12:15350237
|
G | T | 37 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(34): Show | 37 | HG00597.hp1 HG00673.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+27436G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15350237 | ||||||
| chr12:15350333
|
G | A | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0163others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+27532G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15350333 | ||||||
| chr12:15350471
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+27670A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15350471 | ||||||
| chr12:15350474
|
A | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+27673A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15350474 | ||||||
| chr12:15350533
|
T | C | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+27732T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15350533 | ||||||
| chr12:15350637
|
T | C | 5 | a0001c0001t0003g0030a0001c0002t0001g0032a0001c0002t0002g0031others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+27836T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15350637 | ||||||
| chr12:15351407
|
T | C | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+28606T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15351407 | ||||||
| chr12:15351652
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.75+28851C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15351652 | ||||||
| chr12:15351673
|
C | G | 1 | a0001c0001t0009g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+28872C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15351673 | ||||||
| chr12:15351856
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG01169.hp1 HG02300.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+29055C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15351856 | ||||||
| chr12:15351923
|
C | T | 2 | a0001c0003t0001g0150a0001c0003t0001g0151 | 2 | NA18961.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.75+29122C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15351923 | ||||||
| chr12:15352378
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.75+29577T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15352378 | ||||||
| chr12:15352456
|
T | C | 1 | a0001c0004t0001g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.75+29655T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15352456 | ||||||
| chr12:15352507
|
C | T | 2 | a0001c0002t0004g0163a0001c0002t0006g0162 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.75+29706C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15352507 | ||||||
| chr12:15352510
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+29709G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15352510 | ||||||
| chr12:15352649
|
CA | C | 120 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(117): Show | 120 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.75+29867delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15352649 | |||||
| chr12:15352659
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0010 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.75+29862_75+29871d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15352659 | |||||
| chr12:15352660
|
AAAAAAAA others(2): Show |
A | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(22): Show | 25 | HG01123.hp2 HG01169.hp1 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.75+29863_75+29871d others(11): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15352660 | |||||
| chr12:15352665
|
A | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0002g0146others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+29864A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15352665 | ||||||
| chr12:15352667
|
AAG | A | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+29868_75+29869d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15352667 | |||||
| chr12:15352725
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.75+29924A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15352725 | ||||||
| chr12:15352797
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00735.hp1 HG01123.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.75+29996C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15352797 | ||||||
| chr12:15353043
|
A | G | 1 | a0001c0003t0001g0047 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.75+30242A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353043 | ||||||
| chr12:15353382
|
G | A | 1 | a0001c0001t0009g0015 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.75+30581G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353382 | ||||||
| chr12:15353414
|
G | GT | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.75+30624dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15353414 | |||||
| chr12:15353539
|
C | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+30738C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353539 | ||||||
| chr12:15353639
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+30838A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353639 | ||||||
| chr12:15353707
|
T | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+30906T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353707 | ||||||
| chr12:15353754
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.75+30953G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353754 | ||||||
| chr12:15353972
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+31171C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353972 | ||||||
| chr12:15353973
|
T | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+31172T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15353973 | ||||||
| chr12:15354218
|
T | C | 23 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0078others(20): Show | 23 | HG00733.hp1 HG01109.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.75+31417T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354218 | ||||||
| chr12:15354289
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 87 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.75+31488G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354289 | ||||||
| chr12:15354315
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.75+31514C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354315 | ||||||
| chr12:15354353
|
T | G | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+31552T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354353 | ||||||
| chr12:15354481
|
G | T | 1 | a0001c0005t0005g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.75+31680G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354481 | ||||||
| chr12:15354646
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+31845G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354646 | ||||||
| chr12:15354780
|
G | A | 1 | a0001c0001t0003g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.75+31979G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354780 | ||||||
| chr12:15354828
|
A | G | 1 | a0001c0002t0004g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.75+32027A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15354828 | ||||||
| chr12:15355097
|
G | A | 9 | a0001c0001t0001g0160a0001c0002t0002g0131a0001c0002t0002g0135others(6): Show | 9 | HG01515.hp2 HG02809.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+32296G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355097 | ||||||
| chr12:15355139
|
T | C | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+32338T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355139 | ||||||
| chr12:15355243
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+32442A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355243 | ||||||
| chr12:15355287
|
C | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+32486C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355287 | ||||||
| chr12:15355307
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+32506G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355307 | ||||||
| chr12:15355342
|
G | A | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+32541G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355342 | ||||||
| chr12:15355376
|
C | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+32575C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355376 | ||||||
| chr12:15355526
|
TG | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+32727delG | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15355526 | |||||
| chr12:15355546
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0020 | 3 | NA18943.hp2 NA18981.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.75+32745A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355546 | ||||||
| chr12:15355809
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+33008G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355809 | ||||||
| chr12:15355885
|
T | C | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+33084T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355885 | ||||||
| chr12:15355894
|
C | G | 1 | a0001c0003t0001g0145 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.75+33093C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15355894 | ||||||
| chr12:15356514
|
C | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+33713C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15356514 | ||||||
| chr12:15356657
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+33856C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15356657 | ||||||
| chr12:15356871
|
G | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+34070G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15356871 | ||||||
| chr12:15356903
|
G | T | 1 | a0001c0002t0002g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.75+34102G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15356903 | ||||||
| chr12:15356925
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+34124C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15356925 | ||||||
| chr12:15357553
|
A | G | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75+34752A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15357553 | ||||||
| chr12:15357681
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+34880G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15357681 | ||||||
| chr12:15357819
|
T | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+35018T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15357819 | ||||||
| chr12:15357828
|
T | C | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+35027T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15357828 | ||||||
| chr12:15357988
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+35187A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15357988 | ||||||
| chr12:15358076
|
T | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+35275T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15358076 | ||||||
| chr12:15358171
|
G | A | 22 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0078others(19): Show | 22 | HG00733.hp1 HG01109.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.75+35370G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15358171 | ||||||
| chr12:15358652
|
A | C | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.75+35851A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15358652 | ||||||
| chr12:15358727
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.75+35926C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15358727 | ||||||
| chr12:15358860
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+36059G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15358860 | ||||||
| chr12:15359053
|
C | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+36252C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359053 | ||||||
| chr12:15359110
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+36309G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359110 | ||||||
| chr12:15359203
|
A | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+36402A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359203 | ||||||
| chr12:15359227
|
G | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+36426G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359227 | ||||||
| chr12:15359422
|
C | CT | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(28): Show | 31 | HG00621.hp2 HG00735.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.75+36641dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15359422 | |||||
| chr12:15359422
|
C | CTT | 6 | a0001c0002t0003g0028a0001c0002t0003g0079a0001c0002t0006g0162others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+36640_75+36641d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15359422 | |||||
| chr12:15359422
|
C | CTTT | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0163others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+36639_75+36641d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15359422 | |||||
| chr12:15359559
|
C | T | 1 | a0001c0002t0003g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.75+36758C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359559 | ||||||
| chr12:15359570
|
T | TTTTA | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+36786_75+36789d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15359570 | |||||
| chr12:15359630
|
G | T | 5 | a0001c0001t0001g0049a0001c0003t0001g0051a0001c0004t0001g0055others(2): Show | 5 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+36829G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359630 | ||||||
| chr12:15359683
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+36882C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359683 | ||||||
| chr12:15359865
|
T | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+37064T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359865 | ||||||
| chr12:15359930
|
T | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+37129T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359930 | ||||||
| chr12:15359972
|
T | G | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.75+37171T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15359972 | ||||||
| chr12:15360256
|
A | T | 1 | a0001c0006t0004g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.75+37455A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360256 | ||||||
| chr12:15360400
|
G | A | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+37599G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360400 | ||||||
| chr12:15360605
|
T | TTC | 2 | a0001c0002t0006g0058a0001c0002t0006g0059 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.75+37818_75+37819d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360605 | |||||
| chr12:15360621
|
A | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0020others(30): Show | 33 | HG00733.hp1 HG01109.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.75+37820A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360621 | ||||||
| chr12:15360629
|
ATG | A | 4 | a0001c0001t0001g0130a0001c0001t0002g0146a0001c0001t0002g0149others(1): Show | 4 | HG02300.hp2 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+37838_75+37839d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360629 | |||||
| chr12:15360656
|
G | A | 7 | a0001c0004t0001g0099a0001c0004t0001g0100a0001c0005t0002g0109others(4): Show | 7 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+37855G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360656 | ||||||
| chr12:15360668
|
C | G | 8 | a0001c0001t0001g0160a0001c0003t0001g0150a0001c0003t0001g0151others(5): Show | 8 | HG01515.hp2 HG03704.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+37867C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360668 | ||||||
| chr12:15360764
|
G | GTATATAT others(59): Show |
1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.75+37991_75+38056d others(68): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360764 | |||||
| chr12:15360784
|
A | G | 1 | a0001c0004t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+37983A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360784 | ||||||
| chr12:15360807
|
T | C | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+38006T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360807 | ||||||
| chr12:15360828
|
GTA | G | 2 | a0001c0002t0012g0084a0001c0003t0001g0012 | 2 | HG02717.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.75+38036_75+38037d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360828 | |||||
| chr12:15360830
|
A | ATATACAC others(5): Show |
26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.75+38033_75+38034i others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360830 | |||||
| chr12:15360832
|
A | ATACACGT others(3): Show |
7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+38033_75+38034i others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360832 | |||||
| chr12:15360835
|
T | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+38034T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360835 | ||||||
| chr12:15360836
|
ATACGTGT others(9): Show |
A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+38037_75+38052d others(18): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360836 | |||||
| chr12:15360837
|
T | C | 2 | a0001c0002t0012g0084a0001c0003t0001g0012 | 2 | HG02717.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.75+38036T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360837 | ||||||
| chr12:15360838
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.75+38037A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360838 | ||||||
| chr12:15360839
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+38038C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360839 | ||||||
| chr12:15360840
|
G | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+38039G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360840 | ||||||
| chr12:15360851
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+38050T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360851 | ||||||
| chr12:15360852
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+38051G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360852 | ||||||
| chr12:15360852
|
G | GTGTGTAT others(5): Show |
1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+38056_75+38057i others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360852 | |||||
| chr12:15360852
|
G | GTGTGTGT others(5): Show |
1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+38064_75+38075d others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360852 | |||||
| chr12:15360853
|
T | C | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+38052T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360853 | ||||||
| chr12:15360853
|
T | TGTGTGTA others(7): Show |
1 | a0001c0003t0001g0012 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.75+38063_75+38064i others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360853 | |||||
| chr12:15360858
|
G | A | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+38057G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360858 | ||||||
| chr12:15360863
|
T | C | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+38062T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360863 | ||||||
| chr12:15360865
|
T | C | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+38064T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360865 | ||||||
| chr12:15360875
|
T | TATGTGTG others(31): Show |
1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+38075_75+38076i others(40): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360875 | |||||
| chr12:15360879
|
C | T | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+38078C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360879 | ||||||
| chr12:15360881
|
C | T | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+38080C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360881 | ||||||
| chr12:15360883
|
TAC | T | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+38086_75+38087d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360883 | |||||
| chr12:15360889
|
T | C | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+38088T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360889 | ||||||
| chr12:15360889
|
T | TGTGTGTA others(49): Show |
7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+38092_75+38093i others(58): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360889 | |||||
| chr12:15360890
|
G | GTGTGTAT others(21): Show |
23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+38092_75+38093i others(30): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360890 | |||||
| chr12:15360894
|
A | G | 5 | a0001c0002t0001g0019a0001c0002t0003g0028a0001c0002t0004g0163others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+38093A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360894 | ||||||
| chr12:15360899
|
C | T | 4 | a0001c0002t0003g0028a0001c0002t0004g0163a0001c0002t0008g0027others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+38098C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360899 | ||||||
| chr12:15360907
|
T | C | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.75+38106T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360907 | ||||||
| chr12:15360911
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.75+38110T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360911 | ||||||
| chr12:15360918
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.75+38117A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360918 | ||||||
| chr12:15360935
|
T | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+38134T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360935 | ||||||
| chr12:15360945
|
C | CGTGTATA others(21): Show |
3 | a0001c0002t0001g0019a0001c0002t0003g0028a0001c0003t0001g0026 | 3 | HG02723.hp2 HG03195.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.75+38171_75+38172i others(30): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360945 | |||||
| chr12:15360945
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+38144C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360945 | ||||||
| chr12:15360969
|
C | CACATGTG others(19): Show |
1 | a0001c0002t0008g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+38171_75+38172i others(28): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15360969 | |||||
| chr12:15360976
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+38175A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15360976 | ||||||
| chr12:15361153
|
A | G | 2 | a0001c0001t0001g0148a0001c0004t0001g0147 | 2 | HG01074.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.75+38352A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15361153 | ||||||
| chr12:15361160
|
G | A | 2 | a0001c0004t0001g0055a0001c0007t0001g0053 | 2 | HG00423.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.75+38359G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15361160 | ||||||
| chr12:15361176
|
G | A | 4 | a0001c0002t0002g0076a0001c0002t0005g0075a0001c0003t0001g0074others(1): Show | 4 | HG00733.hp1 HG01884.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+38375G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15361176 | ||||||
| chr12:15361332
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+38531G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15361332 | ||||||
| chr12:15361343
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+38542A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15361343 | ||||||
| chr12:15361382
|
T | C | 12 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+38581T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15361382 | ||||||
| chr12:15361438
|
CAA | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+38656_75+38657d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15361438 | |||||
| chr12:15361893
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.75+39092A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15361893 | ||||||
| chr12:15362305
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+39504A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15362305 | ||||||
| chr12:15362500
|
T | C | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+39699T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15362500 | ||||||
| chr12:15362782
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+39981C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15362782 | ||||||
| chr12:15362821
|
T | C | 28 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0110others(25): Show | 28 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.75+40020T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15362821 | ||||||
| chr12:15363011
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 76 | HG00597.hp1 HG00673.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.75+40210C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15363011 | ||||||
| chr12:15363354
|
C | A | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+40553C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15363354 | ||||||
| chr12:15363658
|
AC | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+40858delC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15363658 | ||||||
| chr12:15363659
|
C | T | 2 | a0001c0002t0003g0079a0001c0002t0006g0162 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.75+40858C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15363659 | ||||||
| chr12:15363660
|
TA | T | 9 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0009g0046others(6): Show | 9 | HG00597.hp1 HG00673.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+40870delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15363660 | |||||
| chr12:15363661
|
A | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+40860A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15363661 | ||||||
| chr12:15363920
|
C | T | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+41119C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15363920 | ||||||
| chr12:15364210
|
G | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0003t0001g0036 | 3 | HG01934.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.75+41409G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364210 | ||||||
| chr12:15364270
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+41469C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364270 | ||||||
| chr12:15364445
|
T | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+41644T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364445 | ||||||
| chr12:15364533
|
C | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+41732C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364533 | ||||||
| chr12:15364546
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+41745C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364546 | ||||||
| chr12:15364558
|
C | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.75+41757C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364558 | ||||||
| chr12:15364581
|
T | A | 2 | a0001c0002t0001g0137a0001c0002t0003g0129 | 2 | HG01167.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.75+41780T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364581 | ||||||
| chr12:15364741
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+41940A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364741 | ||||||
| chr12:15364820
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+42019C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15364820 | ||||||
| chr12:15365045
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.75+42244A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365045 | ||||||
| chr12:15365277
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+42476A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365277 | ||||||
| chr12:15365320
|
A | G | 1 | a0001c0003t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.75+42519A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365320 | ||||||
| chr12:15365323
|
T | G | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+42522T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365323 | ||||||
| chr12:15365366
|
C | CTGTTTGA others(4): Show |
1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.75+42571_75+42581d others(13): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15365366 | |||||
| chr12:15365412
|
T | TTA | 9 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+42625_75+42626d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15365412 | |||||
| chr12:15365476
|
C | T | 1 | a0001c0003t0001g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.75+42675C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365476 | ||||||
| chr12:15365647
|
T | C | 60 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(57): Show | 60 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.75+42846T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365647 | ||||||
| chr12:15365700
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.75+42899T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365700 | ||||||
| chr12:15365892
|
A | G | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+43091A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365892 | ||||||
| chr12:15365948
|
T | C | 71 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(68): Show | 71 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.75+43147T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365948 | ||||||
| chr12:15365950
|
T | G | 62 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.75+43149T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15365950 | ||||||
| chr12:15366168
|
T | C | 2 | a0001c0002t0001g0137a0001c0002t0003g0129 | 2 | HG01167.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.75+43367T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15366168 | ||||||
| chr12:15366357
|
AG | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.75+43563delG | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15366357 | |||||
| chr12:15366372
|
T | A | 70 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(67): Show | 70 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.75+43571T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15366372 | ||||||
| chr12:15366379
|
A | G | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75+43578A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15366379 | ||||||
| chr12:15366466
|
T | A | 60 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(57): Show | 60 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.75+43665T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15366466 | ||||||
| chr12:15366655
|
G | T | 1 | a0001c0001t0002g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.75+43854G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15366655 | ||||||
| chr12:15366656
|
G | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+43855G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15366656 | ||||||
| chr12:15367069
|
A | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.75+44268A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367069 | ||||||
| chr12:15367071
|
T | A | 1 | a0001c0002t0001g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.75+44270T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367071 | ||||||
| chr12:15367139
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+44338T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367139 | ||||||
| chr12:15367324
|
A | G | 70 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(67): Show | 70 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.75+44523A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367324 | ||||||
| chr12:15367346
|
C | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+44545C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367346 | ||||||
| chr12:15367364
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+44563G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367364 | ||||||
| chr12:15367421
|
C | A | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+44620C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367421 | ||||||
| chr12:15367476
|
G | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+44675G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367476 | ||||||
| chr12:15367795
|
G | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.75+44994G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367795 | ||||||
| chr12:15367908
|
G | A | 70 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(67): Show | 70 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.75+45107G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15367908 | ||||||
| chr12:15368041
|
A | T | 59 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(56): Show | 59 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.75+45240A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368041 | ||||||
| chr12:15368106
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.75+45305C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368106 | ||||||
| chr12:15368115
|
C | G | 1 | a0001c0001t0009g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+45314C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368115 | ||||||
| chr12:15368250
|
A | G | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+45449A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368250 | ||||||
| chr12:15368251
|
T | C | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+45450T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368251 | ||||||
| chr12:15368670
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+45869A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368670 | ||||||
| chr12:15368719
|
T | C | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+45918T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368719 | ||||||
| chr12:15368836
|
C | G | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+46035C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368836 | ||||||
| chr12:15368860
|
G | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+46059G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368860 | ||||||
| chr12:15368924
|
C | T | 60 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(57): Show | 60 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.75+46123C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368924 | ||||||
| chr12:15368951
|
G | A | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+46150G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368951 | ||||||
| chr12:15368989
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+46188G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15368989 | ||||||
| chr12:15369221
|
G | A | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+46420G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369221 | ||||||
| chr12:15369261
|
T | C | 1 | a0001c0002t0003g0057 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.75+46460T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369261 | ||||||
| chr12:15369341
|
A | C | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+46540A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369341 | ||||||
| chr12:15369434
|
T | A | 60 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(57): Show | 60 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.75+46633T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369434 | ||||||
| chr12:15369435
|
C | A | 60 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(57): Show | 60 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.75+46634C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369435 | ||||||
| chr12:15369438
|
T | A | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+46637T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369438 | ||||||
| chr12:15369444
|
C | A | 6 | a0001c0001t0001g0049a0001c0002t0004g0056a0001c0003t0001g0051others(3): Show | 6 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+46643C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369444 | ||||||
| chr12:15369445
|
G | A | 1 | a0001c0001t0009g0015 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.75+46644G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369445 | ||||||
| chr12:15369627
|
T | C | 7 | a0001c0004t0001g0099a0001c0004t0001g0100a0001c0005t0002g0109others(4): Show | 7 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+46826T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369627 | ||||||
| chr12:15369977
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.75+47176G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369977 | ||||||
| chr12:15369999
|
A | C | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+47198A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15369999 | ||||||
| chr12:15370051
|
CA | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.75+47258delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15370051 | |||||
| chr12:15370242
|
G | A | 1 | a0001c0003t0007g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.75+47441G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370242 | ||||||
| chr12:15370338
|
T | C | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+47537T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370338 | ||||||
| chr12:15370344
|
AT | A | 12 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+47544delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370344 | ||||||
| chr12:15370395
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.75+47594C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370395 | ||||||
| chr12:15370433
|
A | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.75+47632A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370433 | ||||||
| chr12:15370475
|
T | C | 1 | a0001c0005t0005g0096 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.75+47674T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370475 | ||||||
| chr12:15370529
|
C | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+47728C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370529 | ||||||
| chr12:15370586
|
G | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0128others(6): Show | 9 | HG00597.hp2 HG01074.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+47785G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370586 | ||||||
| chr12:15370665
|
A | C | 2 | a0001c0003t0001g0051a0003c0010t0013g0054 | 2 | HG02683.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.75+47864A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370665 | ||||||
| chr12:15370943
|
G | C | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+48142G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15370943 | ||||||
| chr12:15371025
|
T | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.75+48224T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371025 | ||||||
| chr12:15371096
|
T | A | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+48295T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371096 | ||||||
| chr12:15371140
|
A | G | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+48339A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371140 | ||||||
| chr12:15371236
|
TA | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+48436delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371236 | ||||||
| chr12:15371237
|
A | T | 158 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(155): Show | 158 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(155): Show |
intron_variant | MODIFIER | c.75+48436A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371237 | ||||||
| chr12:15371380
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.75+48579C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371380 | ||||||
| chr12:15371387
|
A | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0073others(12): Show | 15 | HG00597.hp1 HG00673.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+48586A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371387 | ||||||
| chr12:15371434
|
T | C | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+48633T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371434 | ||||||
| chr12:15371546
|
A | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+48745A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371546 | ||||||
| chr12:15371694
|
A | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+48893A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371694 | ||||||
| chr12:15371785
|
C | T | 1 | a0001c0002t0001g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+48984C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371785 | ||||||
| chr12:15371878
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+49077C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371878 | ||||||
| chr12:15371879
|
G | A | 1 | a0001c0007t0001g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.75+49078G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15371879 | ||||||
| chr12:15372430
|
C | T | 1 | a0001c0007t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.75+49629C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372430 | ||||||
| chr12:15372465
|
C | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+49664C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372465 | ||||||
| chr12:15372564
|
G | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+49763G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372564 | ||||||
| chr12:15372630
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.75+49829G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372630 | ||||||
| chr12:15372756
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+49955A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372756 | ||||||
| chr12:15372767
|
T | C | 5 | a0001c0001t0003g0030a0001c0002t0001g0032a0001c0002t0002g0031others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+49966T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372767 | ||||||
| chr12:15372845
|
A | G | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+50044A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372845 | ||||||
| chr12:15372850
|
A | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0125others(8): Show | 11 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+50049A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15372850 | ||||||
| chr12:15373261
|
T | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+50460T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373261 | ||||||
| chr12:15373276
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+50475G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373276 | ||||||
| chr12:15373295
|
A | G | 2 | a0001c0004t0001g0007a0002c0011t0001g0092 | 2 | HG01169.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.75+50494A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373295 | ||||||
| chr12:15373434
|
G | A | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+50633G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373434 | ||||||
| chr12:15373459
|
G | A | 61 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+50658G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373459 | ||||||
| chr12:15373652
|
T | G | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+50851T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373652 | ||||||
| chr12:15373672
|
T | C | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+50871T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373672 | ||||||
| chr12:15373678
|
A | G | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+50877A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373678 | ||||||
| chr12:15373732
|
C | A | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+50931C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373732 | ||||||
| chr12:15373772
|
A | G | 1 | a0001c0002t0003g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.75+50971A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15373772 | ||||||
| chr12:15374121
|
C | A | 49 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(46): Show | 49 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+51320C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15374121 | ||||||
| chr12:15374169
|
T | C | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75+51368T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15374169 | ||||||
| chr12:15374411
|
TA | T | 49 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(46): Show | 49 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+51617delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15374411 | |||||
| chr12:15374446
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+51645G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15374446 | ||||||
| chr12:15374899
|
C | T | 2 | a0001c0001t0001g0148a0001c0004t0001g0147 | 2 | HG01074.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.75+52098C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15374899 | ||||||
| chr12:15374986
|
A | G | 70 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(67): Show | 70 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.75+52185A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15374986 | ||||||
| chr12:15375004
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+52203A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375004 | ||||||
| chr12:15375044
|
A | G | 62 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.75+52243A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375044 | ||||||
| chr12:15375115
|
A | G | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+52314A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375115 | ||||||
| chr12:15375124
|
G | A | 70 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(67): Show | 70 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.75+52323G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375124 | ||||||
| chr12:15375548
|
C | G | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+52747C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375548 | ||||||
| chr12:15375618
|
C | T | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+52817C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375618 | ||||||
| chr12:15375760
|
C | CA | 27 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0049others(24): Show | 27 | HG00423.hp1 HG00673.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.75+52978dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15375760 | |||||
| chr12:15375760
|
C | CAAA | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+52976_75+52978d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15375760 | |||||
| chr12:15375760
|
CA | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0110others(4): Show | 7 | HG01074.hp2 HG01515.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+52978delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15375760 | |||||
| chr12:15375760
|
CAA | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(21): Show | 24 | HG00735.hp1 HG01981.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+52977_75+52978d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15375760 | |||||
| chr12:15375909
|
G | C | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+53108G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375909 | ||||||
| chr12:15375935
|
C | T | 70 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(67): Show | 70 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.75+53134C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375935 | ||||||
| chr12:15375946
|
T | C | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+53145T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15375946 | ||||||
| chr12:15376353
|
A | C | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+53552A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376353 | ||||||
| chr12:15376588
|
C | T | 1 | a0001c0002t0001g0013 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.75+53787C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376588 | ||||||
| chr12:15376658
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+53857C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376658 | ||||||
| chr12:15376664
|
G | A | 51 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(48): Show | 51 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.75+53863G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376664 | ||||||
| chr12:15376740
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+53939G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376740 | ||||||
| chr12:15376777
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0122a0001c0003t0001g0106others(1): Show | 4 | HG02083.hp1 NA18988.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+53976C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376777 | ||||||
| chr12:15376869
|
T | C | 51 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(48): Show | 51 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.75+54068T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376869 | ||||||
| chr12:15376968
|
G | T | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.75+54167G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15376968 | ||||||
| chr12:15377018
|
A | C | 11 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0003g0060others(8): Show | 11 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+54217A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15377018 | ||||||
| chr12:15377528
|
TA | T | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+54730delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15377528 | |||||
| chr12:15378173
|
T | TA | 13 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0006g0068others(10): Show | 13 | HG00733.hp1 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+55372_75+55373i others(3): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15378173 | ||||||
| chr12:15378174
|
T | A | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+55373T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15378174 | ||||||
| chr12:15378807
|
C | T | 70 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(67): Show | 70 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.75+56006C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15378807 | ||||||
| chr12:15379365
|
CA | C | 53 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(50): Show | 53 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.75+56580delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15379365 | |||||
| chr12:15379381
|
A | T | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+56580A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379381 | ||||||
| chr12:15379444
|
C | G | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+56643C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379444 | ||||||
| chr12:15379528
|
C | G | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+56727C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379528 | ||||||
| chr12:15379530
|
C | CA | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00597.hp2 HG00735.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.75+56751dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15379530 | |||||
| chr12:15379530
|
C | CAA | 11 | a0001c0001t0001g0010a0001c0001t0005g0102a0001c0001t0005g0103others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+56750_75+56751d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15379530 | |||||
| chr12:15379530
|
CA | C | 6 | a0001c0001t0001g0160a0001c0001t0002g0069a0001c0003t0001g0038others(3): Show | 6 | HG01515.hp2 HG02145.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+56751delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15379530 | |||||
| chr12:15379530
|
CAA | C | 7 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+56750_75+56751d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15379530 | |||||
| chr12:15379656
|
T | C | 2 | a0001c0003t0001g0051a0003c0010t0013g0054 | 2 | HG02683.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.75+56855T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379656 | ||||||
| chr12:15379819
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+57018T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379819 | ||||||
| chr12:15379853
|
G | C | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+57052G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379853 | ||||||
| chr12:15379929
|
G | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+57128G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379929 | ||||||
| chr12:15379955
|
T | C | 40 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.75+57154T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379955 | ||||||
| chr12:15379957
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(13): Show | 16 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+57156T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379957 | ||||||
| chr12:15379976
|
A | T | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+57175A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15379976 | ||||||
| chr12:15380078
|
A | G | 1 | a0001c0004t0002g0127 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.75+57277A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380078 | ||||||
| chr12:15380111
|
T | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+57310T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380111 | ||||||
| chr12:15380197
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.75+57396G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380197 | ||||||
| chr12:15380437
|
C | T | 40 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.75+57636C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380437 | ||||||
| chr12:15380493
|
A | G | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+57692A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380493 | ||||||
| chr12:15380636
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02300.hp1 HG02738.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+57835T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380636 | ||||||
| chr12:15380798
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.75+57997T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380798 | ||||||
| chr12:15380821
|
G | T | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+58020G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380821 | ||||||
| chr12:15380834
|
T | G | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+58033T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380834 | ||||||
| chr12:15380880
|
A | C | 2 | a0001c0002t0007g0080a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.75+58079A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380880 | ||||||
| chr12:15380921
|
A | G | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.75+58120A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15380921 | ||||||
| chr12:15381120
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+58319C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15381120 | ||||||
| chr12:15381377
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+58576A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15381377 | ||||||
| chr12:15381392
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.75+58591C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15381392 | ||||||
| chr12:15381459
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.75+58658C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15381459 | ||||||
| chr12:15381592
|
T | C | 71 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(68): Show | 71 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.75+58791T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15381592 | ||||||
| chr12:15381714
|
T | C | 51 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(48): Show | 51 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.75+58913T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15381714 | ||||||
| chr12:15382078
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.75+59277A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15382078 | ||||||
| chr12:15382159
|
A | AAT | 13 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0006g0068others(10): Show | 13 | HG00733.hp1 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+59375_75+59376d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15382159 | |||||
| chr12:15382159
|
A | AATAT | 27 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0078others(24): Show | 27 | HG00597.hp1 HG00673.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.75+59373_75+59376d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15382159 | |||||
| chr12:15382159
|
A | AATATATA others(1): Show |
6 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0003t0001g0051others(3): Show | 6 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+59369_75+59376d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15382159 | |||||
| chr12:15382159
|
A | AATATATA others(3): Show |
3 | a0001c0002t0008g0052a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG03195.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+59367_75+59376d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15382159 | |||||
| chr12:15382362
|
C | T | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+59561C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15382362 | ||||||
| chr12:15383086
|
C | T | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+60285C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15383086 | ||||||
| chr12:15383171
|
C | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+60370C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15383171 | ||||||
| chr12:15383320
|
T | G | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+60519T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15383320 | ||||||
| chr12:15383333
|
C | CAT | 33 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(30): Show | 33 | HG00597.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+60540_75+60541d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15383333 | |||||
| chr12:15383333
|
C | CATAT | 8 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0002t0004g0056others(5): Show | 8 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+60538_75+60541d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15383333 | |||||
| chr12:15383505
|
T | G | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+60704T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15383505 | ||||||
| chr12:15383554
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+60753C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15383554 | ||||||
| chr12:15383862
|
T | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0006g0068others(11): Show | 14 | HG00733.hp1 HG01261.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+61061T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15383862 | ||||||
| chr12:15384118
|
T | C | 51 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(48): Show | 51 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.75+61317T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384118 | ||||||
| chr12:15384292
|
T | C | 51 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(48): Show | 51 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.75+61491T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384292 | ||||||
| chr12:15384348
|
G | A | 5 | a0001c0001t0003g0030a0001c0002t0001g0032a0001c0002t0002g0031others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+61547G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384348 | ||||||
| chr12:15384400
|
A | G | 1 | a0001c0002t0006g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.75+61599A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384400 | ||||||
| chr12:15384646
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02738.hp2 NA18962.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+61845T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384646 | ||||||
| chr12:15384765
|
T | C | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+61964T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384765 | ||||||
| chr12:15384863
|
T | C | 41 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(38): Show | 41 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.75+62062T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384863 | ||||||
| chr12:15384903
|
A | C | 51 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(48): Show | 51 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.75+62102A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384903 | ||||||
| chr12:15384981
|
A | T | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+62180A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15384981 | ||||||
| chr12:15385259
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.75+62458A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15385259 | ||||||
| chr12:15385348
|
A | T | 1 | a0001c0001t0004g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.75+62547A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15385348 | ||||||
| chr12:15385449
|
G | A | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75+62648G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15385449 | ||||||
| chr12:15385811
|
C | CA | 42 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(39): Show | 42 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.75+63032dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15385811 | |||||
| chr12:15385811
|
CA | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0126others(2): Show | 5 | HG01074.hp1 HG03098.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+63032delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15385811 | |||||
| chr12:15385881
|
G | T | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+63080G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15385881 | ||||||
| chr12:15385932
|
G | T | 1 | a0001c0006t0004g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.75+63131G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15385932 | ||||||
| chr12:15386249
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+63448T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386249 | ||||||
| chr12:15386398
|
C | A | 2 | a0001c0001t0001g0134a0001c0002t0003g0143 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.75+63597C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386398 | ||||||
| chr12:15386423
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.75+63622C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386423 | ||||||
| chr12:15386507
|
A | G | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.75+63706A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386507 | ||||||
| chr12:15386557
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+63756T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386557 | ||||||
| chr12:15386751
|
G | A | 11 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+63950G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386751 | ||||||
| chr12:15386837
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.75+64036G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386837 | ||||||
| chr12:15386838
|
T | C | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+64037T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15386838 | ||||||
| chr12:15387078
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+64277T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15387078 | ||||||
| chr12:15387557
|
C | T | 2 | a0001c0002t0007g0080a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.75+64756C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15387557 | ||||||
| chr12:15387934
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+65133A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15387934 | ||||||
| chr12:15388041
|
C | G | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.75+65240C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388041 | ||||||
| chr12:15388070
|
G | A | 40 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.75+65269G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388070 | ||||||
| chr12:15388203
|
C | G | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+65402C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388203 | ||||||
| chr12:15388208
|
G | A | 71 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(68): Show | 71 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.75+65407G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388208 | ||||||
| chr12:15388278
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.75+65477T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388278 | ||||||
| chr12:15388302
|
A | G | 1 | a0001c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.75+65501A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388302 | ||||||
| chr12:15388304
|
A | T | 2 | a0001c0002t0002g0076a0001c0002t0005g0075 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.75+65503A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388304 | ||||||
| chr12:15388334
|
T | C | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+65533T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388334 | ||||||
| chr12:15388458
|
G | C | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+65657G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388458 | ||||||
| chr12:15388598
|
T | C | 50 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+65797T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388598 | ||||||
| chr12:15388892
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+66091C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388892 | ||||||
| chr12:15388982
|
A | C | 20 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0090others(17): Show | 20 | HG01167.hp2 HG01516.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.75+66181A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15388982 | ||||||
| chr12:15389104
|
A | AT | 26 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0073others(23): Show | 26 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.75+66320dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15389104 | |||||
| chr12:15389104
|
A | ATT | 35 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0049others(32): Show | 35 | HG00423.hp1 HG00733.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.75+66319_75+66320d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15389104 | |||||
| chr12:15389104
|
A | ATTT | 6 | a0001c0002t0002g0063a0001c0002t0002g0064a0001c0002t0002g0065others(3): Show | 6 | HG01109.hp1 HG02723.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+66318_75+66320d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15389104 | |||||
| chr12:15389126
|
CAG | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0020 | 3 | NA18943.hp2 NA18981.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.75+66328_75+66329d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15389126 | |||||
| chr12:15389200
|
T | C | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+66399T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15389200 | ||||||
| chr12:15389301
|
G | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+66500G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15389301 | ||||||
| chr12:15389328
|
C | T | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+66527C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15389328 | ||||||
| chr12:15389386
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.75+66585C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15389386 | ||||||
| chr12:15389852
|
T | C | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+67051T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15389852 | ||||||
| chr12:15390042
|
A | T | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.75+67241A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390042 | ||||||
| chr12:15390322
|
G | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+67521G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390322 | ||||||
| chr12:15390338
|
A | G | 1 | a0001c0002t0008g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+67537A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390338 | ||||||
| chr12:15390486
|
A | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.75+67685A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390486 | ||||||
| chr12:15390545
|
C | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 46 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.75+67744C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390545 | ||||||
| chr12:15390582
|
G | A | 1 | a0001c0003t0001g0036 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.75+67781G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390582 | ||||||
| chr12:15390637
|
A | T | 1 | a0001c0004t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.75+67836A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390637 | ||||||
| chr12:15390733
|
A | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+67932A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390733 | ||||||
| chr12:15390757
|
GGTAAGAG others(9): Show |
G | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+67958_75+67973d others(18): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15390757 | |||||
| chr12:15390810
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.75+68009T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390810 | ||||||
| chr12:15390824
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.75+68023T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390824 | ||||||
| chr12:15390972
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+68171A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390972 | ||||||
| chr12:15390997
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+68196G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15390997 | ||||||
| chr12:15391112
|
T | C | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+68311T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391112 | ||||||
| chr12:15391139
|
G | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+68338G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391139 | ||||||
| chr12:15391149
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.75+68348G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391149 | ||||||
| chr12:15391175
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+68374C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391175 | ||||||
| chr12:15391372
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+68571T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391372 | ||||||
| chr12:15391465
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.75+68664T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391465 | ||||||
| chr12:15391476
|
C | T | 8 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0004g0034others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+68675C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391476 | ||||||
| chr12:15391597
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.75+68796C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391597 | ||||||
| chr12:15391606
|
C | T | 7 | a0001c0001t0007g0083a0001c0001t0007g0085a0001c0002t0007g0080others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+68805C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391606 | ||||||
| chr12:15391661
|
C | A | 1 | a0001c0004t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.75+68860C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391661 | ||||||
| chr12:15391692
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+68891G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391692 | ||||||
| chr12:15391941
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.75+69140C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391941 | ||||||
| chr12:15391954
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 83 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.75+69153T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15391954 | ||||||
| chr12:15392045
|
G | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+69244G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392045 | ||||||
| chr12:15392194
|
C | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.75+69393C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392194 | ||||||
| chr12:15392209
|
A | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(53): Show | 56 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.75+69408A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392209 | ||||||
| chr12:15392247
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(52): Show | 55 | HG00733.hp2 HG00735.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.75+69446G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392247 | ||||||
| chr12:15392468
|
C | G | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+69667C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392468 | ||||||
| chr12:15392512
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 68 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.75+69711A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392512 | ||||||
| chr12:15392712
|
C | A | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.75+69911C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392712 | ||||||
| chr12:15392720
|
C | CA | 22 | a0001c0001t0001g0049a0001c0001t0001g0078a0001c0001t0001g0101others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.75+69941dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15392720 | |||||
| chr12:15392720
|
C | CAAAAAA | 6 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+69936_75+69941d others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15392720 | |||||
| chr12:15392720
|
C | CAAAAAAA | 15 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(12): Show | 15 | HG01515.hp1 HG01981.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+69935_75+69941d others(9): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15392720 | |||||
| chr12:15392720
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(7): Show | 10 | HG00735.hp1 HG02630.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+69934_75+69941d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15392720 | |||||
| chr12:15392720
|
CA | C | 10 | a0001c0001t0001g0093a0001c0001t0006g0068a0001c0002t0001g0077others(7): Show | 10 | HG00735.hp2 HG01167.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+69941delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15392720 | |||||
| chr12:15392740
|
A | G | 1 | a0001c0001t0009g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+69939A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15392740 | ||||||
| chr12:15393224
|
A | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+70423A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15393224 | ||||||
| chr12:15393628
|
AT | A | 15 | a0001c0001t0005g0102a0001c0001t0006g0094a0001c0002t0001g0019others(12): Show | 15 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+70843delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15393628 | |||||
| chr12:15393628
|
ATT | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00735.hp1 HG01109.hp2 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+70842_75+70843d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15393628 | |||||
| chr12:15393840
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+71039A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15393840 | ||||||
| chr12:15393893
|
A | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+71092A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15393893 | ||||||
| chr12:15393894
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+71093G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15393894 | ||||||
| chr12:15394244
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(22): Show | 25 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.75+71443A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394244 | ||||||
| chr12:15394341
|
A | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.75+71540A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394341 | ||||||
| chr12:15394376
|
G | A | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+71575G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394376 | ||||||
| chr12:15394383
|
A | G | 1 | a0001c0003t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.75+71582A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394383 | ||||||
| chr12:15394635
|
T | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+71834T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394635 | ||||||
| chr12:15394698
|
A | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.75+71897A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394698 | ||||||
| chr12:15394730
|
T | C | 2 | a0001c0001t0001g0134a0001c0002t0003g0143 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.75+71929T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394730 | ||||||
| chr12:15394746
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(29): Show | 32 | HG00735.hp1 HG01123.hp2 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.75+71945A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394746 | ||||||
| chr12:15394776
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.75+71975G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15394776 | ||||||
| chr12:15395211
|
G | C | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+72410G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15395211 | ||||||
| chr12:15395218
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+72417T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15395218 | ||||||
| chr12:15395525
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+72724A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15395525 | ||||||
| chr12:15395564
|
C | T | 15 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0073others(12): Show | 15 | HG00597.hp1 HG00673.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+72763C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15395564 | ||||||
| chr12:15395809
|
T | TCA | 28 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0090others(25): Show | 28 | HG01074.hp1 HG01167.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.75+73038_75+73039d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15395809 | |||||
| chr12:15395809
|
T | TCACA | 2 | a0001c0003t0001g0106a0001c0003t0001g0145 | 2 | HG01516.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.75+73036_75+73039d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15395809 | |||||
| chr12:15395809
|
TCA | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0029others(55): Show | 58 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.75+73038_75+73039d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15395809 | |||||
| chr12:15395809
|
TCACA | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(27): Show | 30 | HG00733.hp2 HG00735.hp1 HG01981.hp2 others(27): Show |
intron_variant | MODIFIER | c.75+73036_75+73039d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15395809 | |||||
| chr12:15396060
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+73259T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15396060 | ||||||
| chr12:15396314
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+73513A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15396314 | ||||||
| chr12:15396443
|
CA | C | 5 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0004t0001g0005others(2): Show | 5 | HG02300.hp1 HG02738.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+73650delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15396443 | |||||
| chr12:15396460
|
G | A | 11 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+73659G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15396460 | ||||||
| chr12:15396468
|
GA | G | 12 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+73675delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15396468 | |||||
| chr12:15396716
|
T | C | 7 | a0001c0001t0001g0049a0001c0002t0004g0056a0001c0002t0008g0052others(4): Show | 7 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+73915T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15396716 | ||||||
| chr12:15396727
|
T | C | 1 | a0001c0002t0002g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.75+73926T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15396727 | ||||||
| chr12:15397018
|
A | AT | 13 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+74225dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15397018 | |||||
| chr12:15397371
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+74570T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15397371 | ||||||
| chr12:15397679
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.75+74878C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15397679 | ||||||
| chr12:15397719
|
C | G | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+74918C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15397719 | ||||||
| chr12:15397870
|
A | AAGGTAGG others(1): Show |
9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+75070_75+75077d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15397870 | |||||
| chr12:15398045
|
G | C | 5 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+75244G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15398045 | ||||||
| chr12:15398690
|
CT | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(45): Show | 48 | HG00423.hp1 HG00735.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.75+75900delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15398690 | |||||
| chr12:15398720
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.75+75919G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15398720 | ||||||
| chr12:15398877
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0002g0069others(30): Show | 33 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.75+76076C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15398877 | ||||||
| chr12:15398900
|
C | T | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+76099C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15398900 | ||||||
| chr12:15398980
|
C | T | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+76179C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15398980 | ||||||
| chr12:15399043
|
A | G | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.75+76242A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399043 | ||||||
| chr12:15399462
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+76661A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399462 | ||||||
| chr12:15399485
|
A | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+76684A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399485 | ||||||
| chr12:15399660
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+76859G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399660 | ||||||
| chr12:15399697
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.75+76896G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399697 | ||||||
| chr12:15399773
|
C | G | 11 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+76972C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399773 | ||||||
| chr12:15399844
|
G | A | 1 | a0001c0003t0001g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.75+77043G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399844 | ||||||
| chr12:15399846
|
T | C | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+77045T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399846 | ||||||
| chr12:15399848
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+77047C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399848 | ||||||
| chr12:15399911
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0105others(3): Show | 6 | HG02083.hp1 NA18942.hp1 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+77110C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15399911 | ||||||
| chr12:15400004
|
T | C | 2 | a0001c0003t0001g0051a0003c0010t0013g0054 | 2 | HG02683.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.75+77203T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15400004 | ||||||
| chr12:15400051
|
CA | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0044others(11): Show | 14 | HG00597.hp1 HG00673.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+77269delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15400051 | |||||
| chr12:15400051
|
CAA | C | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+77268_75+77269d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15400051 | |||||
| chr12:15400253
|
C | T | 2 | a0001c0004t0001g0024a0001c0004t0001g0025 | 2 | NA18989.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.75+77452C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15400253 | ||||||
| chr12:15400484
|
G | A | 13 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(10): Show | 13 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+77683G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15400484 | ||||||
| chr12:15400795
|
A | G | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+77994A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15400795 | ||||||
| chr12:15401312
|
G | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00423.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.75+78511G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15401312 | ||||||
| chr12:15401668
|
T | C | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+78867T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15401668 | ||||||
| chr12:15402280
|
G | T | 12 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+79479G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15402280 | ||||||
| chr12:15402296
|
G | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+79495G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15402296 | ||||||
| chr12:15402311
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+79510C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15402311 | ||||||
| chr12:15402939
|
C | G | 24 | a0001c0001t0001g0004a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+80138C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15402939 | ||||||
| chr12:15403097
|
T | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+80296T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403097 | ||||||
| chr12:15403223
|
G | A | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+80422G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403223 | ||||||
| chr12:15403455
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-80519C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403455 | ||||||
| chr12:15403578
|
G | A | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-80396G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403578 | ||||||
| chr12:15403697
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0136a0001c0002t0001g0139others(1): Show | 4 | HG02074.hp2 NA18943.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-80277A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403697 | ||||||
| chr12:15403746
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-80228G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403746 | ||||||
| chr12:15403820
|
G | GAC | 13 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(10): Show | 13 | HG00423.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-80139_76-80138d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15403820 | |||||
| chr12:15403821
|
A | T | 1 | a0001c0003t0001g0074 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.76-80153A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403821 | ||||||
| chr12:15403854
|
G | A | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.76-80120G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15403854 | ||||||
| chr12:15404012
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.76-79962C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404012 | ||||||
| chr12:15404068
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-79906T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404068 | ||||||
| chr12:15404146
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(12): Show | 15 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.76-79828G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404146 | ||||||
| chr12:15404188
|
C | CA | 31 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0037others(28): Show | 31 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-79762dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15404188 | |||||
| chr12:15404188
|
CA | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0119others(21): Show | 24 | HG00423.hp1 HG01074.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-79762delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15404188 | |||||
| chr12:15404188
|
CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-79769_76-79762d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15404188 | |||||
| chr12:15404454
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.76-79520T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404454 | ||||||
| chr12:15404598
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.76-79376C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404598 | ||||||
| chr12:15404610
|
T | A | 1 | a0001c0001t0009g0015 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.76-79364T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404610 | ||||||
| chr12:15404748
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.76-79226A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404748 | ||||||
| chr12:15404909
|
A | G | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-79065A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404909 | ||||||
| chr12:15404918
|
C | T | 2 | a0001c0001t0001g0148a0001c0004t0001g0147 | 2 | HG01074.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.76-79056C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15404918 | ||||||
| chr12:15405043
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0004t0001g0005others(2): Show | 5 | HG02300.hp1 HG02738.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-78931C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405043 | ||||||
| chr12:15405085
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-78889T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405085 | ||||||
| chr12:15405125
|
A | G | 1 | a0001c0006t0004g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.76-78849A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405125 | ||||||
| chr12:15405197
|
A | G | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-78777A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405197 | ||||||
| chr12:15405217
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-78757G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405217 | ||||||
| chr12:15405372
|
CT | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.76-78598delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15405372 | |||||
| chr12:15405405
|
A | G | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.76-78569A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405405 | ||||||
| chr12:15405532
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00735.hp1 HG01515.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.76-78442A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405532 | ||||||
| chr12:15405605
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.76-78369T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15405605 | ||||||
| chr12:15406285
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.76-77689G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15406285 | ||||||
| chr12:15406611
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.76-77363G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15406611 | ||||||
| chr12:15406630
|
C | G | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-77344C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15406630 | ||||||
| chr12:15406715
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-77259T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15406715 | ||||||
| chr12:15406976
|
A | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-76998A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15406976 | ||||||
| chr12:15407262
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(123): Show | 126 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.76-76712A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15407262 | ||||||
| chr12:15407400
|
A | G | 1 | a0001c0007t0001g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.76-76574A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15407400 | ||||||
| chr12:15407405
|
T | A | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.76-76569T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15407405 | ||||||
| chr12:15407499
|
G | A | 15 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0110others(12): Show | 15 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-76475G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15407499 | ||||||
| chr12:15407607
|
CTA | C | 24 | a0001c0001t0001g0004a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-76362_76-76361d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15407607 | |||||
| chr12:15407822
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0004t0001g0005others(2): Show | 5 | HG02300.hp1 HG02738.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-76152G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15407822 | ||||||
| chr12:15408210
|
CT | C | 7 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0003g0079others(4): Show | 7 | HG02300.hp1 HG02451.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-75755delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15408210 | |||||
| chr12:15408278
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-75696G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15408278 | ||||||
| chr12:15408708
|
G | A | 1 | a0001c0003t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.76-75266G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15408708 | ||||||
| chr12:15408842
|
C | T | 69 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(66): Show | 69 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.76-75132C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15408842 | ||||||
| chr12:15408865
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(76): Show | 79 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.76-75109A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15408865 | ||||||
| chr12:15408954
|
T | C | 1 | a0001c0001t0006g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.76-75020T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15408954 | ||||||
| chr12:15409343
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-74631T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15409343 | ||||||
| chr12:15409436
|
C | T | 11 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0073others(8): Show | 11 | HG00597.hp1 HG00673.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-74538C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15409436 | ||||||
| chr12:15409613
|
A | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-74361A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15409613 | ||||||
| chr12:15409614
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-74360T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15409614 | ||||||
| chr12:15409713
|
GC | G | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0050others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-74260delC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15409713 | ||||||
| chr12:15409727
|
A | T | 11 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-74247A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15409727 | ||||||
| chr12:15410182
|
TA | T | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-73789delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15410182 | |||||
| chr12:15410194
|
A | G | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-73780A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410194 | ||||||
| chr12:15410364
|
G | C | 8 | a0001c0001t0001g0049a0001c0002t0008g0052a0001c0003t0001g0051others(5): Show | 8 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-73610G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410364 | ||||||
| chr12:15410426
|
C | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(21): Show | 24 | HG00423.hp1 HG00735.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-73548C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410426 | ||||||
| chr12:15410441
|
A | C | 1 | a0001c0006t0004g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.76-73533A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410441 | ||||||
| chr12:15410525
|
A | G | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.76-73449A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410525 | ||||||
| chr12:15410709
|
G | A | 1 | a0001c0006t0004g0152 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.76-73265G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410709 | ||||||
| chr12:15410729
|
C | G | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-73245C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410729 | ||||||
| chr12:15410773
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-73201G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15410773 | ||||||
| chr12:15411066
|
G | A | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-72908G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15411066 | ||||||
| chr12:15411354
|
A | G | 1 | a0001c0006t0004g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.76-72620A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15411354 | ||||||
| chr12:15411740
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0093others(1): Show | 4 | HG00621.hp1 HG00735.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-72234A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15411740 | ||||||
| chr12:15412168
|
GA | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0002g0069others(30): Show | 33 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-71800delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15412168 | |||||
| chr12:15412177
|
C | T | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.76-71797C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412177 | ||||||
| chr12:15412300
|
A | G | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-71674A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412300 | ||||||
| chr12:15412305
|
A | T | 11 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-71669A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412305 | ||||||
| chr12:15412729
|
T | A | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-71245T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412729 | ||||||
| chr12:15412745
|
A | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.76-71229A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412745 | ||||||
| chr12:15412828
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.76-71146C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412828 | ||||||
| chr12:15412868
|
A | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0002g0069others(31): Show | 34 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.76-71106A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412868 | ||||||
| chr12:15412871
|
A | T | 11 | a0001c0001t0001g0004a0001c0001t0008g0011a0001c0002t0004g0034others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-71103A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412871 | ||||||
| chr12:15412886
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.76-71088C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412886 | ||||||
| chr12:15412928
|
G | A | 2 | a0001c0001t0001g0148a0001c0004t0001g0147 | 2 | HG01074.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.76-71046G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15412928 | ||||||
| chr12:15413038
|
C | T | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-70936C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15413038 | ||||||
| chr12:15413282
|
A | G | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.76-70692A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15413282 | ||||||
| chr12:15413435
|
T | C | 2 | a0001c0001t0001g0110a0001c0003t0001g0124 | 2 | HG00621.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.76-70539T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15413435 | ||||||
| chr12:15413770
|
G | C | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-70204G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15413770 | ||||||
| chr12:15413823
|
C | CAAAT | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-70135_76-70132d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15413823 | |||||
| chr12:15413906
|
T | TA | 5 | a0001c0001t0001g0049a0001c0003t0001g0051a0001c0004t0001g0055others(2): Show | 5 | HG00423.hp1 HG01243.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-70060dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15413906 | |||||
| chr12:15414186
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.76-69788C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15414186 | ||||||
| chr12:15414511
|
G | GA | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.76-69461dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15414511 | |||||
| chr12:15414575
|
T | C | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-69399T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15414575 | ||||||
| chr12:15414701
|
C | A | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-69273C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15414701 | ||||||
| chr12:15414729
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-69245G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15414729 | ||||||
| chr12:15414951
|
G | A | 1 | a0001c0003t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.76-69023G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15414951 | ||||||
| chr12:15414989
|
G | A | 19 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0090others(16): Show | 19 | HG01167.hp2 HG01516.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-68985G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15414989 | ||||||
| chr12:15415046
|
C | T | 11 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-68928C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415046 | ||||||
| chr12:15415232
|
C | A | 1 | a0001c0002t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.76-68742C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415232 | ||||||
| chr12:15415233
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.76-68741A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415233 | ||||||
| chr12:15415320
|
G | A | 14 | a0001c0001t0001g0088a0001c0001t0001g0105a0001c0001t0001g0110others(11): Show | 14 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-68654G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415320 | ||||||
| chr12:15415386
|
A | AT | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-68572dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15415386 | |||||
| chr12:15415386
|
AT | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.76-68572delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15415386 | |||||
| chr12:15415529
|
C | T | 22 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0091others(19): Show | 22 | HG01167.hp2 HG01516.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.76-68445C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415529 | ||||||
| chr12:15415530
|
A | G | 22 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0091others(19): Show | 22 | HG01167.hp2 HG01516.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.76-68444A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415530 | ||||||
| chr12:15415533
|
T | C | 22 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0091others(19): Show | 22 | HG01167.hp2 HG01516.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.76-68441T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415533 | ||||||
| chr12:15415548
|
C | CTAATT | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02630.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.76-68424_76-68420d others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15415548 | |||||
| chr12:15415549
|
TAATTTTT others(5131): Show |
T | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-68423_76-63286d others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15415549 | |||||
| chr12:15415575
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 115 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.76-68399G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415575 | ||||||
| chr12:15415576
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.76-68398G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415576 | ||||||
| chr12:15415577
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.76-68397G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415577 | ||||||
| chr12:15415584
|
CT | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0111 | 2 | HG00735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.76-68389delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415584 | ||||||
| chr12:15415587
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.76-68387A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415587 | ||||||
| chr12:15415596
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0105 | 2 | NA18943.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.76-68378A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415596 | ||||||
| chr12:15415614
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0120 | 2 | HG01074.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.76-68360C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415614 | ||||||
| chr12:15415620
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.76-68354T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415620 | ||||||
| chr12:15415680
|
C | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0126others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-68294C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415680 | ||||||
| chr12:15415912
|
G | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0003t0001g0038others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-68062G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15415912 | ||||||
| chr12:15415924
|
CT | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0003t0001g0038others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-68048delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15415924 | |||||
| chr12:15416229
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.76-67745C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15416229 | ||||||
| chr12:15416230
|
G | A | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0002t0003g0079others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-67744G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15416230 | ||||||
| chr12:15416325
|
C | CT | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 81 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.76-67637dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15416325 | |||||
| chr12:15416325
|
C | CTT | 35 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0093others(32): Show | 35 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.76-67638_76-67637d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15416325 | |||||
| chr12:15416358
|
C | T | 8 | a0001c0001t0001g0049a0001c0002t0001g0032a0001c0002t0002g0031others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-67616C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15416358 | ||||||
| chr12:15416562
|
G | T | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.76-67412G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15416562 | ||||||
| chr12:15416619
|
G | A | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.76-67355G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15416619 | ||||||
| chr12:15416721
|
C | CT | 26 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0086others(23): Show | 26 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.76-67238dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15416721 | |||||
| chr12:15416721
|
CT | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0093others(45): Show | 48 | HG00597.hp2 HG00733.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.76-67238delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15416721 | |||||
| chr12:15416736
|
T | C | 1 | a0001c0002t0001g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.76-67238T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15416736 | ||||||
| chr12:15417145
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-66829G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417145 | ||||||
| chr12:15417170
|
C | A | 2 | a0001c0001t0004g0115a0001c0002t0016g0061 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.76-66804C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417170 | ||||||
| chr12:15417213
|
G | T | 20 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0110others(17): Show | 20 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-66761G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417213 | ||||||
| chr12:15417353
|
C | G | 11 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(8): Show | 11 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-66621C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417353 | ||||||
| chr12:15417393
|
C | T | 1 | a0001c0003t0001g0047 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.76-66581C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417393 | ||||||
| chr12:15417516
|
G | A | 9 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0002t0001g0032others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-66458G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417516 | ||||||
| chr12:15417858
|
A | G | 1 | a0001c0002t0001g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.76-66116A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417858 | ||||||
| chr12:15417876
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-66098C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15417876 | ||||||
| chr12:15418113
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.76-65861T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15418113 | ||||||
| chr12:15418301
|
A | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.76-65673A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15418301 | ||||||
| chr12:15418411
|
C | T | 24 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 24 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-65563C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15418411 | ||||||
| chr12:15418761
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-65213G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15418761 | ||||||
| chr12:15418812
|
C | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-65162C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15418812 | ||||||
| chr12:15418904
|
C | T | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.76-65070C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15418904 | ||||||
| chr12:15419029
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-64945C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419029 | ||||||
| chr12:15419089
|
C | T | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-64885C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419089 | ||||||
| chr12:15419210
|
A | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-64764A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419210 | ||||||
| chr12:15419442
|
G | A | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-64532G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419442 | ||||||
| chr12:15419495
|
A | G | 33 | a0001c0001t0001g0078a0001c0001t0001g0093a0001c0001t0002g0069others(30): Show | 33 | HG00733.hp2 HG00735.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-64479A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419495 | ||||||
| chr12:15419656
|
C | T | 20 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(17): Show | 20 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.76-64318C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419656 | ||||||
| chr12:15419670
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-64304A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419670 | ||||||
| chr12:15419687
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0007g0083others(2): Show | 5 | HG01934.hp2 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-64287G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419687 | ||||||
| chr12:15419735
|
G | GT | 24 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 24 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-64229dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15419735 | |||||
| chr12:15419804
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0105 | 2 | NA18943.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.76-64170A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419804 | ||||||
| chr12:15419913
|
T | C | 21 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0110others(18): Show | 21 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.76-64061T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15419913 | ||||||
| chr12:15420015
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-63959C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420015 | ||||||
| chr12:15420073
|
G | C | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.76-63901G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420073 | ||||||
| chr12:15420078
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-63896C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420078 | ||||||
| chr12:15420148
|
G | GA | 14 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0001t0007g0085others(11): Show | 14 | HG00733.hp2 HG01109.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-63803dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15420148 | |||||
| chr12:15420148
|
GA | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0021others(76): Show | 79 | HG00423.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.76-63803delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15420148 | |||||
| chr12:15420148
|
GAA | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(27): Show | 30 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.76-63804_76-63803d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15420148 | |||||
| chr12:15420148
|
GAAAAAAA others(1): Show |
G | 11 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(8): Show | 11 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-63810_76-63803d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15420148 | |||||
| chr12:15420261
|
G | A | 5 | a0001c0005t0002g0109a0001c0005t0005g0096a0001c0005t0005g0097others(2): Show | 5 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-63713G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420261 | ||||||
| chr12:15420265
|
A | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-63709A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420265 | ||||||
| chr12:15420482
|
A | G | 1 | a0001c0004t0001g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.76-63492A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420482 | ||||||
| chr12:15420483
|
T | C | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.76-63491T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420483 | ||||||
| chr12:15420536
|
A | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.76-63438A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420536 | ||||||
| chr12:15420688
|
A | G | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-63286A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420688 | ||||||
| chr12:15420709
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.76-63265C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15420709 | ||||||
| chr12:15421008
|
T | G | 4 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-62966T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421008 | ||||||
| chr12:15421148
|
G | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(68): Show | 71 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.76-62826G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421148 | ||||||
| chr12:15421217
|
G | A | 5 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0144others(2): Show | 5 | HG02074.hp1 NA18942.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-62757G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421217 | ||||||
| chr12:15421353
|
T | G | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-62621T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421353 | ||||||
| chr12:15421463
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.76-62511G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421463 | ||||||
| chr12:15421473
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.76-62501G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421473 | ||||||
| chr12:15421479
|
G | T | 4 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-62495G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421479 | ||||||
| chr12:15421491
|
T | C | 1 | a0001c0002t0015g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.76-62483T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421491 | ||||||
| chr12:15421834
|
C | T | 4 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-62140C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15421834 | ||||||
| chr12:15422178
|
G | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-61796G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422178 | ||||||
| chr12:15422266
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-61708C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422266 | ||||||
| chr12:15422532
|
C | T | 3 | a0001c0002t0001g0032a0001c0002t0003g0033a0001c0002t0003g0041 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.76-61442C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422532 | ||||||
| chr12:15422608
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-61366A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422608 | ||||||
| chr12:15422669
|
G | A | 1 | a0001c0002t0002g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.76-61305G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422669 | ||||||
| chr12:15422772
|
T | A | 12 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0035others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-61202T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422772 | ||||||
| chr12:15422922
|
C | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-61052C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422922 | ||||||
| chr12:15422925
|
C | T | 4 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-61049C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422925 | ||||||
| chr12:15422931
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.76-61043A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422931 | ||||||
| chr12:15422994
|
T | C | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.76-60980T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15422994 | ||||||
| chr12:15423011
|
T | C | 20 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(17): Show | 20 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.76-60963T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15423011 | ||||||
| chr12:15423252
|
A | G | 1 | a0001c0004t0001g0005 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.76-60722A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15423252 | ||||||
| chr12:15423290
|
T | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-60684T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15423290 | ||||||
| chr12:15423318
|
T | C | 4 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-60656T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15423318 | ||||||
| chr12:15423694
|
T | C | 1 | a0001c0005t0005g0097 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.76-60280T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15423694 | ||||||
| chr12:15423966
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-60008C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15423966 | ||||||
| chr12:15423986
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.76-59988C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15423986 | ||||||
| chr12:15424272
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-59702C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424272 | ||||||
| chr12:15424446
|
T | C | 1 | a0001c0004t0001g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.76-59528T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424446 | ||||||
| chr12:15424569
|
A | T | 12 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(9): Show | 12 | HG00735.hp2 HG01109.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-59405A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424569 | ||||||
| chr12:15424701
|
G | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-59273G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424701 | ||||||
| chr12:15424795
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-59179T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424795 | ||||||
| chr12:15424825
|
A | G | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-59149A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424825 | ||||||
| chr12:15424916
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-59058G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424916 | ||||||
| chr12:15424928
|
G | C | 13 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0002t0001g0032others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-59046G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15424928 | ||||||
| chr12:15425001
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(79): Show | 82 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.76-58973G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15425001 | ||||||
| chr12:15425024
|
C | T | 13 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0002t0001g0032others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-58950C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15425024 | ||||||
| chr12:15425130
|
C | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-58844C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15425130 | ||||||
| chr12:15425191
|
G | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-58783G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15425191 | ||||||
| chr12:15425292
|
A | G | 1 | a0001c0004t0001g0017 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.76-58682A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15425292 | ||||||
| chr12:15425716
|
A | AT | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-58256dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15425716 | |||||
| chr12:15425733
|
T | TTTCATAT others(3): Show |
121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-58241_76-58240i others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15425733 | ||||||
| chr12:15425991
|
T | A | 11 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(8): Show | 11 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-57983T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15425991 | ||||||
| chr12:15426022
|
A | G | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.76-57952A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15426022 | ||||||
| chr12:15426038
|
TA | T | 9 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0002t0001g0032others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-57934delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15426038 | |||||
| chr12:15426156
|
A | G | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-57818A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15426156 | ||||||
| chr12:15426232
|
A | C | 61 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0086others(58): Show | 61 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.76-57742A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15426232 | ||||||
| chr12:15426304
|
G | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0090others(31): Show | 34 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.76-57670G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15426304 | ||||||
| chr12:15426768
|
G | A | 2 | a0001c0001t0006g0094a0001c0002t0015g0095 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.76-57206G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15426768 | ||||||
| chr12:15426801
|
AT | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-57171delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15426801 | |||||
| chr12:15427013
|
C | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-56961C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427013 | ||||||
| chr12:15427136
|
CTA | C | 5 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-56837_76-56836d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427136 | ||||||
| chr12:15427139
|
G | A | 5 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-56835G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427139 | ||||||
| chr12:15427140
|
A | T | 5 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-56834A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427140 | ||||||
| chr12:15427141
|
A | C | 5 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-56833A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427141 | ||||||
| chr12:15427409
|
A | T | 20 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(17): Show | 20 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.76-56565A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427409 | ||||||
| chr12:15427435
|
C | T | 8 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-56539C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427435 | ||||||
| chr12:15427669
|
C | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-56305C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427669 | ||||||
| chr12:15427704
|
T | C | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-56270T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427704 | ||||||
| chr12:15427733
|
G | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-56241G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427733 | ||||||
| chr12:15427819
|
A | T | 8 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-56155A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427819 | ||||||
| chr12:15427820
|
CT | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-56150delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15427820 | |||||
| chr12:15427871
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.76-56103T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15427871 | ||||||
| chr12:15428202
|
C | A | 30 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(27): Show | 30 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.76-55772C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15428202 | ||||||
| chr12:15428249
|
C | T | 1 | a0001c0001t0006g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.76-55725C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15428249 | ||||||
| chr12:15428427
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-55547G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15428427 | ||||||
| chr12:15428858
|
C | A | 4 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-55116C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15428858 | ||||||
| chr12:15428866
|
A | C | 1 | a0001c0003t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.76-55108A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15428866 | ||||||
| chr12:15428876
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-55098T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15428876 | ||||||
| chr12:15429145
|
T | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 93 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.76-54829T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15429145 | ||||||
| chr12:15429357
|
G | A | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-54617G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15429357 | ||||||
| chr12:15429364
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-54610G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15429364 | ||||||
| chr12:15429404
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.76-54570G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15429404 | ||||||
| chr12:15429410
|
G | A | 12 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(9): Show | 12 | HG00735.hp2 HG01109.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-54564G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15429410 | ||||||
| chr12:15429915
|
G | A | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.76-54059G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15429915 | ||||||
| chr12:15430075
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-53899G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15430075 | ||||||
| chr12:15430201
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-53773T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15430201 | ||||||
| chr12:15430228
|
T | C | 30 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0078others(27): Show | 30 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-53746T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15430228 | ||||||
| chr12:15430280
|
G | T | 30 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(27): Show | 30 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.76-53694G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15430280 | ||||||
| chr12:15430704
|
C | G | 3 | a0001c0002t0011g0082a0001c0003t0007g0081a0001c0003t0007g0164 | 3 | HG02109.hp1 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.76-53270C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15430704 | ||||||
| chr12:15430739
|
C | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.76-53235C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15430739 | ||||||
| chr12:15430960
|
A | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(63): Show | 66 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-53014A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15430960 | ||||||
| chr12:15431024
|
TA | T | 3 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0003g0066 | 3 | HG02145.hp1 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.76-52943delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15431024 | |||||
| chr12:15431071
|
A | G | 1 | a0001c0007t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-52903A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431071 | ||||||
| chr12:15431262
|
G | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-52712G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431262 | ||||||
| chr12:15431384
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-52590C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431384 | ||||||
| chr12:15431577
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-52397A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431577 | ||||||
| chr12:15431630
|
G | A | 8 | a0001c0001t0001g0093a0001c0002t0004g0056a0001c0002t0008g0052others(5): Show | 8 | HG00735.hp2 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-52344G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431630 | ||||||
| chr12:15431665
|
T | C | 1 | a0001c0002t0003g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-52309T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431665 | ||||||
| chr12:15431690
|
A | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0090others(36): Show | 39 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.76-52284A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431690 | ||||||
| chr12:15431728
|
T | G | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-52246T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15431728 | ||||||
| chr12:15432133
|
C | T | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.76-51841C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15432133 | ||||||
| chr12:15432175
|
C | T | 8 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-51799C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15432175 | ||||||
| chr12:15432257
|
G | T | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.76-51717G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15432257 | ||||||
| chr12:15432416
|
A | G | 4 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-51558A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15432416 | ||||||
| chr12:15432452
|
T | C | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.76-51522T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15432452 | ||||||
| chr12:15432700
|
T | C | 8 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0002t0001g0032others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-51274T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15432700 | ||||||
| chr12:15432711
|
G | A | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-51263G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15432711 | ||||||
| chr12:15432986
|
TTTG | T | 3 | a0001c0002t0003g0079a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02451.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-50970_76-50968d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15432986 | |||||
| chr12:15433171
|
CT | C | 29 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0104others(26): Show | 29 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.76-50784delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15433171 | |||||
| chr12:15433171
|
CTT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(89): Show | 92 | HG00597.hp1 HG00673.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.76-50785_76-50784d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15433171 | |||||
| chr12:15433316
|
C | T | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.76-50658C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15433316 | ||||||
| chr12:15433389
|
T | A | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.76-50585T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15433389 | ||||||
| chr12:15433438
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.76-50536C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15433438 | ||||||
| chr12:15433720
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0009g0015a0001c0001t0009g0048 | 3 | HG00621.hp1 HG00673.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.76-50254C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15433720 | ||||||
| chr12:15433747
|
T | G | 18 | a0001c0001t0001g0049a0001c0001t0001g0078a0001c0001t0002g0069others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-50227T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15433747 | ||||||
| chr12:15433898
|
C | T | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-50076C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15433898 | ||||||
| chr12:15433952
|
G | T | 16 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.76-50022G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15433952 | ||||||
| chr12:15434147
|
C | A | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-49827C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434147 | ||||||
| chr12:15434286
|
T | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-49688T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434286 | ||||||
| chr12:15434545
|
G | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-49429G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434545 | ||||||
| chr12:15434624
|
C | T | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-49350C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434624 | ||||||
| chr12:15434875
|
C | T | 8 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-49099C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434875 | ||||||
| chr12:15434883
|
A | G | 8 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-49091A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434883 | ||||||
| chr12:15434933
|
T | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-49041T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434933 | ||||||
| chr12:15434999
|
C | T | 8 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-48975C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15434999 | ||||||
| chr12:15435198
|
G | A | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-48776G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435198 | ||||||
| chr12:15435421
|
C | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-48553C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435421 | ||||||
| chr12:15435558
|
C | CT | 19 | a0001c0001t0001g0093a0001c0001t0003g0030a0001c0001t0005g0102others(16): Show | 19 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.76-48405dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15435558 | |||||
| chr12:15435656
|
G | T | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-48318G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435656 | ||||||
| chr12:15435738
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.76-48236G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435738 | ||||||
| chr12:15435744
|
A | G | 4 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-48230A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435744 | ||||||
| chr12:15435967
|
G | A | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-48007G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435967 | ||||||
| chr12:15435974
|
C | A | 1 | a0001c0002t0001g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.76-48000C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435974 | ||||||
| chr12:15435980
|
C | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-47994C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15435980 | ||||||
| chr12:15436020
|
A | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0088others(31): Show | 34 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.76-47954A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15436020 | ||||||
| chr12:15436031
|
A | G | 20 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0110others(17): Show | 20 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-47943A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15436031 | ||||||
| chr12:15436329
|
T | C | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-47645T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15436329 | ||||||
| chr12:15436375
|
T | C | 18 | a0001c0001t0001g0093a0001c0001t0003g0030a0001c0001t0005g0102others(15): Show | 18 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-47599T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15436375 | ||||||
| chr12:15436631
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.76-47343C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15436631 | ||||||
| chr12:15436893
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-47081C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15436893 | ||||||
| chr12:15437043
|
G | A | 3 | a0001c0002t0001g0032a0001c0002t0003g0033a0001c0002t0003g0041 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.76-46931G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437043 | ||||||
| chr12:15437072
|
G | A | 16 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.76-46902G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437072 | ||||||
| chr12:15437168
|
G | A | 2 | a0001c0002t0001g0137a0001c0002t0003g0129 | 2 | HG01167.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.76-46806G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437168 | ||||||
| chr12:15437250
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.76-46724C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437250 | ||||||
| chr12:15437252
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-46722C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437252 | ||||||
| chr12:15437336
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0008g0011a0001c0004t0002g0161 | 3 | HG03225.hp2 NA18747.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.76-46638G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437336 | ||||||
| chr12:15437406
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-46568C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437406 | ||||||
| chr12:15437682
|
C | T | 8 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-46292C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437682 | ||||||
| chr12:15437732
|
C | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-46242C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437732 | ||||||
| chr12:15437797
|
C | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-46177C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437797 | ||||||
| chr12:15437843
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-46131T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437843 | ||||||
| chr12:15437854
|
G | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-46120G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15437854 | ||||||
| chr12:15438012
|
C | T | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-45962C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15438012 | ||||||
| chr12:15438199
|
A | G | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-45775A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15438199 | ||||||
| chr12:15438484
|
A | G | 1 | a0001c0003t0001g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-45490A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15438484 | ||||||
| chr12:15438545
|
G | C | 35 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0078others(32): Show | 35 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.76-45429G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15438545 | ||||||
| chr12:15438692
|
T | A | 8 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-45282T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15438692 | ||||||
| chr12:15438848
|
T | G | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-45126T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15438848 | ||||||
| chr12:15438970
|
TTTTCCTT others(19): Show |
T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-44993_76-44968d others(28): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15438970 | |||||
| chr12:15439162
|
A | G | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.76-44812A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439162 | ||||||
| chr12:15439256
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.76-44718G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439256 | ||||||
| chr12:15439310
|
C | T | 8 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-44664C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439310 | ||||||
| chr12:15439311
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.76-44663G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439311 | ||||||
| chr12:15439311
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.76-44663G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439311 | ||||||
| chr12:15439352
|
G | A | 1 | a0001c0002t0004g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.76-44622G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439352 | ||||||
| chr12:15439371
|
T | C | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.76-44603T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439371 | ||||||
| chr12:15439399
|
G | A | 8 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-44575G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439399 | ||||||
| chr12:15439483
|
T | C | 1 | a0001c0002t0003g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.76-44491T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439483 | ||||||
| chr12:15439523
|
C | A | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-44451C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439523 | ||||||
| chr12:15439539
|
G | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-44435G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439539 | ||||||
| chr12:15439540
|
C | G | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-44434C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439540 | ||||||
| chr12:15439546
|
G | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-44428G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439546 | ||||||
| chr12:15439560
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0003t0001g0036 | 3 | HG01934.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.76-44414G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439560 | ||||||
| chr12:15439622
|
C | T | 8 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-44352C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439622 | ||||||
| chr12:15439647
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-44327G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439647 | ||||||
| chr12:15439709
|
G | A | 20 | a0001c0001t0001g0093a0001c0001t0003g0030a0001c0001t0005g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.76-44265G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439709 | ||||||
| chr12:15439878
|
G | T | 1 | a0001c0002t0011g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-44096G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439878 | ||||||
| chr12:15439994
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.76-43980G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15439994 | ||||||
| chr12:15440002
|
C | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-43972C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440002 | ||||||
| chr12:15440014
|
T | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-43960T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440014 | ||||||
| chr12:15440176
|
T | C | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-43798T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440176 | ||||||
| chr12:15440181
|
A | G | 1 | a0001c0002t0003g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.76-43793A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440181 | ||||||
| chr12:15440281
|
C | A | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-43693C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440281 | ||||||
| chr12:15440407
|
T | A | 1 | a0001c0002t0004g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.76-43567T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440407 | ||||||
| chr12:15440615
|
C | T | 2 | a0001c0002t0001g0141a0001c0004t0001g0142 | 2 | HG03491.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.76-43359C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440615 | ||||||
| chr12:15440703
|
T | A | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-43271T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440703 | ||||||
| chr12:15440792
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-43182C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440792 | ||||||
| chr12:15440842
|
T | C | 14 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-43132T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440842 | ||||||
| chr12:15440848
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-43126C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15440848 | ||||||
| chr12:15441085
|
A | G | 14 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-42889A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441085 | ||||||
| chr12:15441093
|
A | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-42881A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441093 | ||||||
| chr12:15441120
|
T | C | 8 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-42854T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441120 | ||||||
| chr12:15441208
|
A | C | 2 | a0001c0001t0001g0120a0001c0004t0001g0147 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.76-42766A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441208 | ||||||
| chr12:15441238
|
T | A | 3 | a0001c0001t0001g0049a0001c0001t0008g0011a0001c0004t0002g0161 | 3 | HG03225.hp2 NA18747.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.76-42736T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441238 | ||||||
| chr12:15441238
|
T | C | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-42736T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441238 | ||||||
| chr12:15441251
|
GACTTTTG others(3): Show |
G | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-42721_76-42712d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15441251 | |||||
| chr12:15441319
|
C | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-42655C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441319 | ||||||
| chr12:15441421
|
C | T | 1 | a0001c0002t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.76-42553C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441421 | ||||||
| chr12:15441498
|
C | A | 1 | a0001c0007t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-42476C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441498 | ||||||
| chr12:15441549
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.76-42425A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441549 | ||||||
| chr12:15441702
|
T | C | 23 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0091others(20): Show | 23 | HG00423.hp1 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.76-42272T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441702 | ||||||
| chr12:15441771
|
G | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-42203G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441771 | ||||||
| chr12:15441795
|
A | G | 33 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0078others(30): Show | 33 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-42179A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441795 | ||||||
| chr12:15441893
|
A | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-42081A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441893 | ||||||
| chr12:15441897
|
G | T | 33 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0078others(30): Show | 33 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-42077G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15441897 | ||||||
| chr12:15442068
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-41906C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442068 | ||||||
| chr12:15442096
|
G | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-41878G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442096 | ||||||
| chr12:15442164
|
A | G | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-41810A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442164 | ||||||
| chr12:15442479
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-41495C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442479 | ||||||
| chr12:15442541
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-41433A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442541 | ||||||
| chr12:15442691
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.76-41283C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442691 | ||||||
| chr12:15442732
|
T | A | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.76-41242T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442732 | ||||||
| chr12:15442734
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-41240C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442734 | ||||||
| chr12:15442758
|
A | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-41216A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442758 | ||||||
| chr12:15442907
|
C | A | 14 | a0001c0001t0001g0049a0001c0001t0003g0060a0001c0001t0008g0011others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-41067C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442907 | ||||||
| chr12:15442989
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-40985A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15442989 | ||||||
| chr12:15443113
|
C | T | 2 | a0001c0001t0001g0134a0001c0002t0003g0143 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.76-40861C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15443113 | ||||||
| chr12:15443341
|
A | C | 1 | a0001c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.76-40633A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15443341 | ||||||
| chr12:15443342
|
A | T | 1 | a0001c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.76-40632A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15443342 | ||||||
| chr12:15443810
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.76-40164G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15443810 | ||||||
| chr12:15443994
|
C | A | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.76-39980C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15443994 | ||||||
| chr12:15443994
|
C | CA | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0042others(25): Show | 28 | HG00597.hp1 HG00735.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.76-39966dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15443994 | |||||
| chr12:15443994
|
CA | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0088others(31): Show | 34 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.76-39966delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15443994 | |||||
| chr12:15444012
|
T | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-39962T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15444012 | ||||||
| chr12:15444076
|
A | G | 1 | a0001c0003t0001g0047 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.76-39898A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15444076 | ||||||
| chr12:15444081
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.76-39893C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15444081 | ||||||
| chr12:15444088
|
G | T | 6 | a0001c0001t0003g0030a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-39886G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15444088 | ||||||
| chr12:15444250
|
G | A | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-39724G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15444250 | ||||||
| chr12:15444272
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0078others(30): Show | 33 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-39702C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15444272 | ||||||
| chr12:15444841
|
G | GT | 4 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-39125dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15444841 | |||||
| chr12:15445060
|
T | C | 1 | a0001c0001t0004g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.76-38914T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15445060 | ||||||
| chr12:15445291
|
T | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-38683T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15445291 | ||||||
| chr12:15445317
|
T | C | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-38657T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15445317 | ||||||
| chr12:15445490
|
G | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0101others(20): Show | 23 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-38484G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15445490 | ||||||
| chr12:15445543
|
T | C | 2 | a0001c0001t0001g0134a0001c0002t0003g0143 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.76-38431T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15445543 | ||||||
| chr12:15445669
|
TTACTTTT others(10): Show |
T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-38302_76-38286d others(19): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15445669 | |||||
| chr12:15446045
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0078others(30): Show | 33 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-37929C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15446045 | ||||||
| chr12:15446626
|
T | C | 6 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-37348T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15446626 | ||||||
| chr12:15447200
|
C | T | 1 | a0001c0003t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.76-36774C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447200 | ||||||
| chr12:15447235
|
G | A | 14 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(11): Show | 14 | HG00735.hp2 HG01109.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-36739G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447235 | ||||||
| chr12:15447235
|
G | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-36739G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447235 | ||||||
| chr12:15447335
|
G | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-36639G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447335 | ||||||
| chr12:15447676
|
C | G | 1 | a0001c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.76-36298C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447676 | ||||||
| chr12:15447756
|
CT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-36215delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15447756 | |||||
| chr12:15447812
|
A | G | 1 | a0001c0002t0005g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.76-36162A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447812 | ||||||
| chr12:15447840
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-36134G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447840 | ||||||
| chr12:15447898
|
G | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-36076G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447898 | ||||||
| chr12:15447942
|
C | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-36032C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447942 | ||||||
| chr12:15447945
|
T | C | 1 | a0001c0001t0006g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.76-36029T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15447945 | ||||||
| chr12:15448003
|
T | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-35971T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15448003 | ||||||
| chr12:15448123
|
A | G | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.76-35851A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15448123 | ||||||
| chr12:15448318
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-35656A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15448318 | ||||||
| chr12:15448339
|
T | TA | 8 | a0001c0001t0001g0049a0001c0001t0002g0149a0001c0002t0003g0072others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-35614dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAA | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-35615_76-35614d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAA | 7 | a0001c0001t0001g0078a0001c0002t0001g0077a0001c0002t0002g0062others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-35618_76-35614d others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(2): Show |
36 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(33): Show | 36 | HG00597.hp2 HG01074.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.76-35622_76-35614d others(11): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(3): Show |
13 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0120others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-35623_76-35614d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(4): Show |
4 | a0001c0002t0001g0018a0001c0002t0008g0027a0001c0008t0004g0040others(1): Show | 4 | HG01123.hp2 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-35624_76-35614d others(13): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(5): Show |
2 | a0001c0002t0003g0079a0001c0002t0004g0163 | 2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.76-35625_76-35614d others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(6): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG03017.hp1 NA18962.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-35626_76-35614d others(15): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(7): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0009g0015others(5): Show | 8 | HG00735.hp1 HG01981.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-35627_76-35614d others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(8): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0104others(3): Show | 6 | HG00621.hp1 HG00673.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-35628_76-35614d others(17): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(9): Show |
8 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0134others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-35629_76-35614d others(18): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(10): Show |
5 | a0001c0001t0006g0068a0001c0001t0009g0046a0001c0002t0001g0039others(2): Show | 5 | HG00597.hp1 HG00733.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-35630_76-35614d others(19): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(11): Show |
1 | a0001c0003t0001g0145 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.76-35631_76-35614d others(20): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(12): Show |
11 | a0001c0001t0001g0091a0001c0001t0001g0122a0001c0001t0001g0136others(8): Show | 11 | HG00423.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-35632_76-35614d others(21): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(13): Show |
6 | a0001c0001t0001g0021a0001c0001t0001g0156a0001c0002t0001g0137others(3): Show | 6 | HG01981.hp1 HG02683.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-35633_76-35614d others(22): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(14): Show |
3 | a0001c0001t0001g0126a0001c0002t0001g0019a0001c0002t0001g0087 | 3 | HG04184.hp1 NA19012.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.76-35634_76-35614d others(23): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448339
|
T | TAAAAAAA others(17): Show |
1 | a0001c0002t0001g0013 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.76-35614_76-35613i others(26): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448339 | |||||
| chr12:15448557
|
A | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-35417A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15448557 | ||||||
| chr12:15448611
|
A | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-35363A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15448611 | ||||||
| chr12:15448953
|
C | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-35021C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15448953 | ||||||
| chr12:15448996
|
AAGTT | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(33): Show | 36 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.76-34975_76-34972d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15448996 | |||||
| chr12:15449050
|
A | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-34924A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449050 | ||||||
| chr12:15449056
|
T | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-34918T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449056 | ||||||
| chr12:15449123
|
C | CA | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.76-34838dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15449123 | |||||
| chr12:15449221
|
G | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.76-34753G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449221 | ||||||
| chr12:15449233
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-34741G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449233 | ||||||
| chr12:15449487
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 131 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.76-34487T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449487 | ||||||
| chr12:15449675
|
C | T | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.76-34299C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449675 | ||||||
| chr12:15449705
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(33): Show | 36 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.76-34269T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449705 | ||||||
| chr12:15449773
|
T | C | 22 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(19): Show | 22 | HG00423.hp1 HG01167.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.76-34201T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449773 | ||||||
| chr12:15449876
|
C | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-34098C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15449876 | ||||||
| chr12:15450090
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-33884T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450090 | ||||||
| chr12:15450106
|
C | T | 5 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-33868C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450106 | ||||||
| chr12:15450108
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-33866A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450108 | ||||||
| chr12:15450140
|
AT | A | 5 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(2): Show | 5 | HG01109.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-33829delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15450140 | |||||
| chr12:15450256
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-33718A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450256 | ||||||
| chr12:15450280
|
C | T | 22 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(19): Show | 22 | HG00423.hp1 HG01167.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.76-33694C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450280 | ||||||
| chr12:15450324
|
C | T | 1 | a0001c0002t0015g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.76-33650C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450324 | ||||||
| chr12:15450466
|
A | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 131 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.76-33508A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450466 | ||||||
| chr12:15450481
|
C | G | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-33493C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450481 | ||||||
| chr12:15450507
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-33467C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450507 | ||||||
| chr12:15450628
|
G | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0149 | 2 | HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.76-33346G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450628 | ||||||
| chr12:15450705
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 136 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.76-33269T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450705 | ||||||
| chr12:15450781
|
T | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.76-33193T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450781 | ||||||
| chr12:15450782
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.76-33192T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450782 | ||||||
| chr12:15450789
|
T | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-33185T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450789 | ||||||
| chr12:15450824
|
C | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-33150C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450824 | ||||||
| chr12:15450880
|
C | A | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.76-33094C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450880 | ||||||
| chr12:15450930
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-33044A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15450930 | ||||||
| chr12:15451237
|
G | C | 1 | a0001c0005t0005g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.76-32737G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451237 | ||||||
| chr12:15451346
|
C | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-32628C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451346 | ||||||
| chr12:15451447
|
C | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(33): Show | 36 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.76-32527C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451447 | ||||||
| chr12:15451626
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-32348T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451626 | ||||||
| chr12:15451715
|
T | C | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-32259T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451715 | ||||||
| chr12:15451765
|
C | A | 1 | a0001c0001t0003g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.76-32209C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451765 | ||||||
| chr12:15451813
|
A | G | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.76-32161A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451813 | ||||||
| chr12:15451871
|
T | C | 22 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(19): Show | 22 | HG00423.hp1 HG01167.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.76-32103T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451871 | ||||||
| chr12:15451947
|
A | G | 6 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0003g0079others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-32027A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451947 | ||||||
| chr12:15451954
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.76-32020A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451954 | ||||||
| chr12:15451967
|
C | T | 4 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-32007C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15451967 | ||||||
| chr12:15452044
|
T | C | 6 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0003g0079others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-31930T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452044 | ||||||
| chr12:15452149
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-31825C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452149 | ||||||
| chr12:15452386
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-31588C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452386 | ||||||
| chr12:15452387
|
G | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-31587G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452387 | ||||||
| chr12:15452394
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.76-31580C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452394 | ||||||
| chr12:15452423
|
G | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-31551G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452423 | ||||||
| chr12:15452535
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-31439T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452535 | ||||||
| chr12:15452798
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-31176T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452798 | ||||||
| chr12:15452865
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-31109G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452865 | ||||||
| chr12:15452871
|
C | T | 5 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-31103C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452871 | ||||||
| chr12:15452929
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-31045T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15452929 | ||||||
| chr12:15453034
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.76-30940T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15453034 | ||||||
| chr12:15453141
|
A | C | 1 | a0001c0003t0007g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.76-30833A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15453141 | ||||||
| chr12:15453419
|
T | C | 1 | a0001c0003t0001g0047 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.76-30555T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15453419 | ||||||
| chr12:15453589
|
G | A | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-30385G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15453589 | ||||||
| chr12:15453829
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0105 | 2 | NA18943.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.76-30145T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15453829 | ||||||
| chr12:15453931
|
A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(32): Show | 35 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.76-30043A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15453931 | ||||||
| chr12:15454255
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-29719C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15454255 | ||||||
| chr12:15454361
|
C | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-29613C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15454361 | ||||||
| chr12:15454434
|
G | A | 6 | a0001c0001t0003g0030a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-29540G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15454434 | ||||||
| chr12:15454449
|
T | C | 9 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-29525T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15454449 | ||||||
| chr12:15454570
|
GATATAGT others(9): Show |
G | 2 | a0001c0001t0006g0094a0001c0002t0015g0095 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.76-29385_76-29370d others(18): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15454570 | |||||
| chr12:15454767
|
G | A | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.76-29207G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15454767 | ||||||
| chr12:15454900
|
G | T | 1 | a0001c0001t0009g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.76-29074G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15454900 | ||||||
| chr12:15454931
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-29043A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15454931 | ||||||
| chr12:15455005
|
G | A | 5 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-28969G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455005 | ||||||
| chr12:15455116
|
G | A | 1 | a0001c0002t0004g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.76-28858G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455116 | ||||||
| chr12:15455207
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-28767T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455207 | ||||||
| chr12:15455297
|
C | T | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-28677C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455297 | ||||||
| chr12:15455309
|
T | TC | 11 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0016others(8): Show | 11 | HG02451.hp2 HG02738.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-28658dupC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15455309 | |||||
| chr12:15455313
|
C | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-28661C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455313 | ||||||
| chr12:15455315
|
C | A | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-28659C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455315 | ||||||
| chr12:15455315
|
C | CG | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-28659_76-28658i others(3): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455315 | ||||||
| chr12:15455315
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-28659C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455315 | ||||||
| chr12:15455317
|
A | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-28657A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455317 | ||||||
| chr12:15455574
|
T | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.76-28400T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455574 | ||||||
| chr12:15455635
|
T | A | 5 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-28339T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455635 | ||||||
| chr12:15455645
|
A | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-28329A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455645 | ||||||
| chr12:15455985
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 136 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.76-27989T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455985 | ||||||
| chr12:15455999
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-27975A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15455999 | ||||||
| chr12:15456049
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-27925G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456049 | ||||||
| chr12:15456143
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-27831C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456143 | ||||||
| chr12:15456250
|
C | T | 10 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0001g0077others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-27724C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456250 | ||||||
| chr12:15456262
|
T | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(44): Show | 47 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.76-27712T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456262 | ||||||
| chr12:15456287
|
T | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(32): Show | 35 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.76-27687T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456287 | ||||||
| chr12:15456431
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-27543C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456431 | ||||||
| chr12:15456651
|
G | A | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.76-27323G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456651 | ||||||
| chr12:15456753
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-27221A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456753 | ||||||
| chr12:15456849
|
C | T | 2 | a0001c0002t0007g0080a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.76-27125C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456849 | ||||||
| chr12:15456850
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.76-27124A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456850 | ||||||
| chr12:15456910
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(33): Show | 36 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.76-27064C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456910 | ||||||
| chr12:15456947
|
A | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-27027A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15456947 | ||||||
| chr12:15457139
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.76-26835C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457139 | ||||||
| chr12:15457163
|
C | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.76-26811C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457163 | ||||||
| chr12:15457171
|
G | A | 8 | a0001c0001t0001g0078a0001c0001t0002g0069a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-26803G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457171 | ||||||
| chr12:15457296
|
T | C | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-26678T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457296 | ||||||
| chr12:15457328
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.76-26646T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457328 | ||||||
| chr12:15457359
|
T | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0086others(33): Show | 36 | HG00597.hp2 HG01074.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.76-26615T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457359 | ||||||
| chr12:15457673
|
C | T | 5 | a0001c0002t0004g0034a0001c0002t0007g0080a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-26301C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457673 | ||||||
| chr12:15457892
|
G | C | 107 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0042others(104): Show | 107 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.76-26082G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457892 | ||||||
| chr12:15457950
|
T | G | 1 | a0001c0003t0001g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-26024T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15457950 | ||||||
| chr12:15458049
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.76-25925G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15458049 | ||||||
| chr12:15458160
|
A | G | 1 | a0001c0006t0004g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.76-25814A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15458160 | ||||||
| chr12:15458249
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.76-25725G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15458249 | ||||||
| chr12:15458436
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-25538C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15458436 | ||||||
| chr12:15458563
|
A | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.76-25411A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15458563 | ||||||
| chr12:15458767
|
T | C | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-25207T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15458767 | ||||||
| chr12:15458928
|
T | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 138 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.76-25046T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15458928 | ||||||
| chr12:15459090
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-24884G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459090 | ||||||
| chr12:15459268
|
G | A | 23 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(20): Show | 23 | HG00423.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-24706G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459268 | ||||||
| chr12:15459434
|
C | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-24540C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459434 | ||||||
| chr12:15459440
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-24534C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459440 | ||||||
| chr12:15459485
|
A | G | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-24489A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459485 | ||||||
| chr12:15459547
|
G | A | 1 | a0001c0002t0003g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-24427G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459547 | ||||||
| chr12:15459863
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.76-24111G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459863 | ||||||
| chr12:15459906
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.76-24068C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459906 | ||||||
| chr12:15459965
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-24009T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15459965 | ||||||
| chr12:15460046
|
T | A | 45 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0086others(42): Show | 45 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.76-23928T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460046 | ||||||
| chr12:15460052
|
G | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.76-23922G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460052 | ||||||
| chr12:15460158
|
C | T | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.76-23816C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460158 | ||||||
| chr12:15460219
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.76-23755T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460219 | ||||||
| chr12:15460260
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.76-23714A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460260 | ||||||
| chr12:15460442
|
A | G | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.76-23532A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460442 | ||||||
| chr12:15460758
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-23216C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460758 | ||||||
| chr12:15460978
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.76-22996G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15460978 | ||||||
| chr12:15461391
|
A | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0134a0001c0001t0004g0115others(5): Show | 8 | HG00597.hp1 HG01261.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-22583A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15461391 | ||||||
| chr12:15461428
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.76-22546C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15461428 | ||||||
| chr12:15461566
|
C | CT | 5 | a0001c0001t0001g0037a0001c0001t0007g0085a0001c0002t0004g0034others(2): Show | 5 | HG02145.hp2 HG02922.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-22386dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15461566 | |||||
| chr12:15461566
|
C | CTT | 9 | a0001c0001t0001g0078a0001c0002t0001g0077a0001c0002t0002g0063others(6): Show | 9 | HG01109.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-22387_76-22386d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15461566 | |||||
| chr12:15461566
|
CT | C | 13 | a0001c0001t0001g0088a0001c0002t0001g0013a0001c0002t0001g0087others(10): Show | 13 | HG02074.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-22386delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15461566 | |||||
| chr12:15461566
|
CTT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.76-22387_76-22386d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15461566 | |||||
| chr12:15461808
|
C | T | 1 | a0001c0005t0002g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.76-22166C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15461808 | ||||||
| chr12:15461878
|
T | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-22096T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15461878 | ||||||
| chr12:15462146
|
C | T | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-21828C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462146 | ||||||
| chr12:15462147
|
G | A | 1 | a0002c0011t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.76-21827G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462147 | ||||||
| chr12:15462170
|
G | A | 1 | a0001c0003t0001g0145 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.76-21804G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462170 | ||||||
| chr12:15462188
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.76-21786A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462188 | ||||||
| chr12:15462244
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-21730T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462244 | ||||||
| chr12:15462419
|
C | A | 1 | a0001c0002t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.76-21555C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462419 | ||||||
| chr12:15462739
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.76-21235G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462739 | ||||||
| chr12:15462936
|
T | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-21038T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15462936 | ||||||
| chr12:15463188
|
G | A | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-20786G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463188 | ||||||
| chr12:15463243
|
A | C | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-20731A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463243 | ||||||
| chr12:15463325
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-20649G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463325 | ||||||
| chr12:15463337
|
G | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0149 | 2 | HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.76-20637G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463337 | ||||||
| chr12:15463610
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.76-20364A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463610 | ||||||
| chr12:15463653
|
C | T | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-20321C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463653 | ||||||
| chr12:15463972
|
T | C | 1 | a0001c0003t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.76-20002T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463972 | ||||||
| chr12:15463974
|
C | G | 4 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-20000C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15463974 | ||||||
| chr12:15464006
|
T | C | 1 | a0001c0003t0001g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-19968T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464006 | ||||||
| chr12:15464318
|
T | C | 1 | a0001c0003t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.76-19656T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464318 | ||||||
| chr12:15464362
|
G | GT | 11 | a0001c0001t0001g0125a0001c0001t0005g0103a0001c0001t0007g0085others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-19603dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15464362 | |||||
| chr12:15464408
|
GCAGTGA | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0093others(22): Show | 25 | HG00735.hp2 HG01123.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-19563_76-19558d others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15464408 | |||||
| chr12:15464505
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.76-19469C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464505 | ||||||
| chr12:15464521
|
A | AT | 76 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0021others(73): Show | 76 | HG00423.hp1 HG01074.hp1 HG01074.hp2 others(73): Show |
intron_variant | MODIFIER | c.76-19449dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15464521 | |||||
| chr12:15464526
|
G | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.76-19448G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464526 | ||||||
| chr12:15464556
|
G | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-19418G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464556 | ||||||
| chr12:15464565
|
A | G | 8 | a0001c0001t0001g0078a0001c0002t0001g0077a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-19409A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464565 | ||||||
| chr12:15464618
|
C | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.76-19356C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464618 | ||||||
| chr12:15464720
|
G | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.76-19254G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464720 | ||||||
| chr12:15464750
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.76-19224G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464750 | ||||||
| chr12:15464817
|
C | A | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-19157C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464817 | ||||||
| chr12:15464950
|
A | C | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-19024A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15464950 | ||||||
| chr12:15465133
|
G | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-18841G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15465133 | ||||||
| chr12:15465171
|
T | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 125 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.76-18803T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15465171 | ||||||
| chr12:15465223
|
G | A | 2 | a0001c0001t0001g0110a0001c0003t0001g0124 | 2 | HG00621.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.76-18751G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15465223 | ||||||
| chr12:15465341
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.76-18633C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15465341 | ||||||
| chr12:15465964
|
T | C | 22 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(19): Show | 22 | HG00597.hp2 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.76-18010T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15465964 | ||||||
| chr12:15466269
|
A | G | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-17705A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15466269 | ||||||
| chr12:15466503
|
A | G | 1 | a0001c0006t0004g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.76-17471A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15466503 | ||||||
| chr12:15466674
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-17300G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15466674 | ||||||
| chr12:15466747
|
G | A | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-17227G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15466747 | ||||||
| chr12:15466889
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0007g0083others(2): Show | 5 | HG01934.hp2 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-17085G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15466889 | ||||||
| chr12:15466972
|
C | T | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-17002C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15466972 | ||||||
| chr12:15467239
|
C | T | 1 | a0001c0003t0001g0150 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-16735C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467239 | ||||||
| chr12:15467315
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.76-16659T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467315 | ||||||
| chr12:15467319
|
T | C | 4 | a0001c0002t0002g0076a0001c0002t0002g0135a0001c0002t0005g0075others(1): Show | 4 | HG01884.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-16655T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467319 | ||||||
| chr12:15467409
|
A | AGT | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.76-16544_76-16543d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467409
|
A | AGTGT | 7 | a0001c0001t0001g0105a0001c0001t0006g0094a0001c0002t0001g0032others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-16546_76-16543d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467409
|
A | AGTGTGT | 26 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0093others(23): Show | 26 | HG00735.hp2 HG01123.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.76-16548_76-16543d others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467409
|
A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0128a0001c0002t0001g0035a0001c0002t0001g0117others(4): Show | 7 | HG01516.hp1 HG02723.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-16550_76-16543d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467409
|
A | AGTGTGTG others(3): Show |
5 | a0001c0001t0001g0134a0001c0001t0004g0115a0001c0001t0006g0068others(2): Show | 5 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-16552_76-16543d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467409
|
A | AGTGTGTG others(5): Show |
2 | a0001c0002t0001g0039a0001c0006t0004g0045 | 2 | HG00597.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.76-16554_76-16543d others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467409
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0042 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.76-16556_76-16543d others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467409
|
AGTGTGT | A | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-16548_76-16543d others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15467409 | |||||
| chr12:15467493
|
T | C | 3 | a0001c0001t0001g0113a0001c0009t0001g0153a0001c0009t0001g0154 | 3 | HG00673.hp1 NA18946.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.76-16481T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467493 | ||||||
| chr12:15467543
|
C | A | 4 | a0001c0002t0004g0034a0001c0002t0004g0163a0001c0008t0004g0040others(1): Show | 4 | HG02922.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-16431C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467543 | ||||||
| chr12:15467584
|
C | A | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.76-16390C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467584 | ||||||
| chr12:15467663
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.76-16311C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467663 | ||||||
| chr12:15467741
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.76-16233T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467741 | ||||||
| chr12:15467765
|
C | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-16209C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467765 | ||||||
| chr12:15467869
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 138 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.76-16105G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467869 | ||||||
| chr12:15467913
|
G | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-16061G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467913 | ||||||
| chr12:15467939
|
T | G | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-16035T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467939 | ||||||
| chr12:15467987
|
T | C | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-15987T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15467987 | ||||||
| chr12:15468086
|
A | T | 4 | a0001c0002t0003g0116a0001c0004t0001g0099a0001c0004t0001g0100others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-15888A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468086 | ||||||
| chr12:15468096
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0101others(17): Show | 20 | HG01123.hp1 HG01123.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-15878G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468096 | ||||||
| chr12:15468219
|
C | G | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-15755C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468219 | ||||||
| chr12:15468232
|
A | G | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-15742A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468232 | ||||||
| chr12:15468267
|
G | C | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-15707G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468267 | ||||||
| chr12:15468323
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.76-15651C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468323 | ||||||
| chr12:15468330
|
G | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-15644G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468330 | ||||||
| chr12:15468343
|
G | A | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-15631G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468343 | ||||||
| chr12:15468448
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-15526G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468448 | ||||||
| chr12:15468482
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.76-15492T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468482 | ||||||
| chr12:15468496
|
G | C | 4 | a0001c0002t0007g0080a0001c0002t0011g0082a0001c0002t0012g0084others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-15478G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468496 | ||||||
| chr12:15468540
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-15434A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468540 | ||||||
| chr12:15468639
|
A | G | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-15335A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468639 | ||||||
| chr12:15468706
|
A | C | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.76-15268A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468706 | ||||||
| chr12:15468742
|
G | A | 31 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(28): Show | 31 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-15232G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15468742 | ||||||
| chr12:15469042
|
C | T | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-14932C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469042 | ||||||
| chr12:15469280
|
G | A | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-14694G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469280 | ||||||
| chr12:15469533
|
T | C | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-14441T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469533 | ||||||
| chr12:15469593
|
C | T | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-14381C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469593 | ||||||
| chr12:15469755
|
G | A | 1 | a0001c0004t0002g0127 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.76-14219G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469755 | ||||||
| chr12:15469767
|
A | AC | 18 | a0001c0001t0001g0006a0001c0001t0001g0101a0001c0001t0001g0111others(15): Show | 18 | HG01123.hp1 HG01123.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-14206dupC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15469767 | |||||
| chr12:15469768
|
C | CA | 30 | a0001c0001t0001g0044a0001c0001t0001g0078a0001c0001t0001g0086others(27): Show | 30 | HG00597.hp2 HG00733.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.76-14187dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15469768 | |||||
| chr12:15469768
|
C | CAA | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(22): Show | 25 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-14188_76-14187d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15469768 | |||||
| chr12:15469768
|
C | CAAA | 24 | a0001c0001t0001g0091a0001c0001t0001g0122a0001c0001t0001g0126others(21): Show | 24 | HG00423.hp1 HG01074.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-14189_76-14187d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15469768 | |||||
| chr12:15469768
|
C | CAAAA | 7 | a0001c0001t0001g0021a0001c0001t0001g0136a0001c0001t0001g0156others(4): Show | 7 | HG01167.hp2 HG01981.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-14190_76-14187d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15469768 | |||||
| chr12:15469768
|
CA | C | 6 | a0001c0001t0008g0011a0001c0002t0003g0072a0001c0002t0006g0058others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-14187delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15469768 | |||||
| chr12:15469768
|
CAAA | C | 6 | a0001c0001t0001g0113a0001c0003t0001g0124a0001c0006t0004g0114others(3): Show | 6 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-14189_76-14187d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15469768 | |||||
| chr12:15469769
|
A | C | 13 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0005g0102others(10): Show | 13 | HG00735.hp2 HG01109.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-14205A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469769 | ||||||
| chr12:15469949
|
A | G | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.76-14025A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469949 | ||||||
| chr12:15469951
|
T | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-14023T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15469951 | ||||||
| chr12:15470155
|
T | C | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-13819T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470155 | ||||||
| chr12:15470175
|
G | T | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-13799G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470175 | ||||||
| chr12:15470334
|
C | A | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-13640C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470334 | ||||||
| chr12:15470567
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-13407T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470567 | ||||||
| chr12:15470583
|
C | T | 14 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(11): Show | 14 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-13391C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470583 | ||||||
| chr12:15470623
|
G | C | 1 | a0001c0001t0004g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.76-13351G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470623 | ||||||
| chr12:15470669
|
A | G | 23 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(20): Show | 23 | HG00423.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-13305A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470669 | ||||||
| chr12:15470705
|
G | C | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-13269G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470705 | ||||||
| chr12:15470877
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.76-13097T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470877 | ||||||
| chr12:15470974
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.76-13000C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15470974 | ||||||
| chr12:15471190
|
G | A | 1 | a0001c0007t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-12784G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15471190 | ||||||
| chr12:15471472
|
A | C | 4 | a0001c0002t0004g0034a0001c0002t0004g0163a0001c0008t0004g0040others(1): Show | 4 | HG02922.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-12502A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15471472 | ||||||
| chr12:15471696
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.76-12278G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15471696 | ||||||
| chr12:15471851
|
T | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-12123T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15471851 | ||||||
| chr12:15471904
|
G | A | 3 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094 | 3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.76-12070G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15471904 | ||||||
| chr12:15471970
|
C | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-12004C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15471970 | ||||||
| chr12:15472008
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.76-11966C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472008 | ||||||
| chr12:15472071
|
A | G | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.76-11903A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472071 | ||||||
| chr12:15472103
|
A | G | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-11871A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472103 | ||||||
| chr12:15472128
|
T | C | 7 | a0001c0001t0001g0078a0001c0002t0002g0062a0001c0002t0002g0063others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-11846T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472128 | ||||||
| chr12:15472431
|
C | T | 23 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(20): Show | 23 | HG00423.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-11543C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472431 | ||||||
| chr12:15472468
|
T | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 138 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.76-11506T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472468 | ||||||
| chr12:15472509
|
C | T | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-11465C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472509 | ||||||
| chr12:15472621
|
G | T | 20 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(17): Show | 20 | HG00597.hp2 HG01074.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.76-11353G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472621 | ||||||
| chr12:15472655
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-11319G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15472655 | ||||||
| chr12:15472773
|
T | TGACACGA | 2 | a0001c0003t0001g0038a0001c0006t0004g0152 | 2 | NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.76-11200_76-11199i others(9): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15472773 | |||||
| chr12:15473110
|
A | C | 1 | a0001c0007t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-10864A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473110 | ||||||
| chr12:15473237
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.76-10737G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473237 | ||||||
| chr12:15473330
|
CG | C | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-10642delG | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15473330 | |||||
| chr12:15473331
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.76-10643G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473331 | ||||||
| chr12:15473392
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.76-10582C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473392 | ||||||
| chr12:15473659
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.76-10315C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473659 | ||||||
| chr12:15473721
|
G | A | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-10253G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473721 | ||||||
| chr12:15473768
|
C | CA | 6 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0001g0110others(3): Show | 6 | HG00423.hp2 HG00621.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-10184dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15473768 | |||||
| chr12:15473768
|
C | CAAAAAAA others(12): Show |
1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-10202_76-10184d others(21): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15473768 | |||||
| chr12:15473768
|
C | CAAAAAAA others(13): Show |
2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-10203_76-10184d others(22): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15473768 | |||||
| chr12:15473768
|
CA | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 103 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.76-10184delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15473768 | |||||
| chr12:15473818
|
A | AAC | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-10152_76-10151d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15473818 | |||||
| chr12:15473878
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-10096C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473878 | ||||||
| chr12:15473958
|
G | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-10016G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473958 | ||||||
| chr12:15473986
|
C | T | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-9988C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473986 | ||||||
| chr12:15473993
|
A | G | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-9981A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15473993 | ||||||
| chr12:15474227
|
C | T | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-9747C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474227 | ||||||
| chr12:15474232
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-9742A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474232 | ||||||
| chr12:15474245
|
C | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.76-9729C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474245 | ||||||
| chr12:15474259
|
G | A | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-9715G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474259 | ||||||
| chr12:15474287
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-9687A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474287 | ||||||
| chr12:15474291
|
G | A | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.76-9683G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474291 | ||||||
| chr12:15474391
|
C | T | 1 | a0001c0001t0004g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.76-9583C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474391 | ||||||
| chr12:15474506
|
C | T | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-9468C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474506 | ||||||
| chr12:15474519
|
T | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.76-9455T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474519 | ||||||
| chr12:15474614
|
C | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(67): Show | 70 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.76-9360C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474614 | ||||||
| chr12:15474831
|
G | A | 31 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(28): Show | 31 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-9143G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474831 | ||||||
| chr12:15474836
|
C | T | 1 | a0001c0003t0001g0047 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.76-9138C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15474836 | ||||||
| chr12:15475129
|
G | A | 11 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(8): Show | 11 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-8845G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475129 | ||||||
| chr12:15475574
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.76-8400G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475574 | ||||||
| chr12:15475592
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 138 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.76-8382G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475592 | ||||||
| chr12:15475735
|
A | C | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-8239A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475735 | ||||||
| chr12:15475751
|
C | G | 11 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(8): Show | 11 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-8223C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475751 | ||||||
| chr12:15475759
|
C | G | 31 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(28): Show | 31 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-8215C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475759 | ||||||
| chr12:15475869
|
A | G | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-8105A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475869 | ||||||
| chr12:15475925
|
C | T | 1 | a0001c0003t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.76-8049C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15475925 | ||||||
| chr12:15476302
|
G | A | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-7672G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15476302 | ||||||
| chr12:15476642
|
C | T | 20 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(17): Show | 20 | HG00597.hp2 HG01074.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.76-7332C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15476642 | ||||||
| chr12:15476732
|
C | CA | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-7236dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15476732 | |||||
| chr12:15476902
|
G | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-7072G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15476902 | ||||||
| chr12:15476933
|
G | A | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-7041G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15476933 | ||||||
| chr12:15476975
|
A | T | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-6999A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15476975 | ||||||
| chr12:15477065
|
A | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 125 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.76-6909A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477065 | ||||||
| chr12:15477110
|
A | C | 4 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094others(1): Show | 4 | HG01109.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-6864A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477110 | ||||||
| chr12:15477237
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-6737A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477237 | ||||||
| chr12:15477245
|
G | A | 2 | a0001c0004t0001g0099a0001c0004t0001g0100 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.76-6729G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477245 | ||||||
| chr12:15477280
|
A | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-6694A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477280 | ||||||
| chr12:15477354
|
G | A | 3 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0094 | 3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.76-6620G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477354 | ||||||
| chr12:15477419
|
C | T | 3 | a0001c0002t0002g0050a0001c0002t0004g0034a0001c0002t0004g0163 | 3 | HG02922.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-6555C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477419 | ||||||
| chr12:15477450
|
A | G | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-6524A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477450 | ||||||
| chr12:15477502
|
TA | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-6463delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15477502 | |||||
| chr12:15477504
|
A | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-6470A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477504 | ||||||
| chr12:15477654
|
C | G | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-6320C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477654 | ||||||
| chr12:15477731
|
A | T | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-6243A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477731 | ||||||
| chr12:15477828
|
A | G | 13 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-6146A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477828 | ||||||
| chr12:15477874
|
G | C | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.76-6100G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477874 | ||||||
| chr12:15477929
|
G | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-6045G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15477929 | ||||||
| chr12:15478056
|
A | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-5918A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478056 | ||||||
| chr12:15478114
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-5860A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478114 | ||||||
| chr12:15478204
|
G | C | 1 | a0001c0002t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.76-5770G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478204 | ||||||
| chr12:15478284
|
G | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-5690G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478284 | ||||||
| chr12:15478341
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-5633A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478341 | ||||||
| chr12:15478455
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.76-5519C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478455 | ||||||
| chr12:15478534
|
C | T | 1 | a0001c0003t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.76-5440C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478534 | ||||||
| chr12:15478570
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-5404A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478570 | ||||||
| chr12:15478611
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.76-5363G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478611 | ||||||
| chr12:15478702
|
C | G | 1 | a0001c0002t0003g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-5272C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478702 | ||||||
| chr12:15478711
|
G | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-5263G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15478711 | ||||||
| chr12:15479013
|
C | G | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.76-4961C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479013 | ||||||
| chr12:15479027
|
C | T | 3 | a0001c0001t0003g0060a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG01884.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-4947C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479027 | ||||||
| chr12:15479091
|
C | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-4883C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479091 | ||||||
| chr12:15479338
|
T | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-4636T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479338 | ||||||
| chr12:15479474
|
A | C | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-4500A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479474 | ||||||
| chr12:15479588
|
C | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-4386C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479588 | ||||||
| chr12:15479757
|
G | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-4217G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479757 | ||||||
| chr12:15479779
|
G | A | 1 | a0002c0011t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.76-4195G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479779 | ||||||
| chr12:15479784
|
G | A | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-4190G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15479784 | ||||||
| chr12:15480017
|
A | G | 3 | a0001c0001t0003g0060a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG01884.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-3957A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480017 | ||||||
| chr12:15480088
|
T | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-3886T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480088 | ||||||
| chr12:15480287
|
T | G | 2 | a0001c0001t0009g0015a0001c0001t0009g0048 | 2 | HG00673.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.76-3687T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480287 | ||||||
| chr12:15480298
|
A | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-3676A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480298 | ||||||
| chr12:15480321
|
A | G | 1 | a0001c0002t0004g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.76-3653A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480321 | ||||||
| chr12:15480566
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.76-3408C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480566 | ||||||
| chr12:15480657
|
G | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-3317G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480657 | ||||||
| chr12:15480713
|
G | A | 1 | a0001c0001t0006g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.76-3261G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480713 | ||||||
| chr12:15480721
|
A | AGATG | 10 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0002t0001g0077others(7): Show | 10 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-3212_76-3209dup others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15480721 | |||||
| chr12:15480721
|
A | AGATGGAT others(1): Show |
2 | a0001c0001t0001g0078a0001c0003t0001g0106 | 2 | HG02895.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.76-3216_76-3209dup others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15480721 | |||||
| chr12:15480721
|
AGATG | A | 28 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(25): Show | 28 | HG02074.hp1 HG02074.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.76-3212_76-3209del others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15480721 | |||||
| chr12:15480721
|
AGATGGAT others(1): Show |
A | 8 | a0001c0001t0001g0073a0001c0001t0001g0113a0001c0003t0001g0051others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-3216_76-3209del others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15480721 | |||||
| chr12:15480721
|
AGATGGAT others(9): Show |
A | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 65 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.76-3224_76-3209del others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15480721 | |||||
| chr12:15480962
|
G | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-3012G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15480962 | ||||||
| chr12:15481150
|
G | T | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-2824G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15481150 | ||||||
| chr12:15481432
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-2542A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15481432 | ||||||
| chr12:15481636
|
G | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-2338G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15481636 | ||||||
| chr12:15482123
|
G | A | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1851G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482123 | ||||||
| chr12:15482144
|
G | GGT | 12 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0002t0001g0039others(9): Show | 12 | HG00597.hp1 HG01109.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-1807_76-1806dup others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15482144 | |||||
| chr12:15482161
|
GTGTGTGT others(1): Show |
G | 10 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-1811_76-1804del others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15482161 | |||||
| chr12:15482165
|
GTGTA | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-1807_76-1804del others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15482165 | |||||
| chr12:15482167
|
G | A | 21 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(18): Show | 21 | HG00597.hp2 HG02074.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.76-1807G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482167 | ||||||
| chr12:15482167
|
G | GTA | 2 | a0001c0001t0001g0120a0001c0004t0001g0147 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.76-1795_76-1794dup others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15482167 | |||||
| chr12:15482169
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.76-1805A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482169 | ||||||
| chr12:15482179
|
ATG | A | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1784_76-1783del others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr12 | 15482179 | |||||
| chr12:15482181
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.76-1793G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482181 | ||||||
| chr12:15482410
|
G | A | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-1564G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482410 | ||||||
| chr12:15482443
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-1531C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482443 | ||||||
| chr12:15482684
|
A | G | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1290A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482684 | ||||||
| chr12:15482723
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.76-1251G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482723 | ||||||
| chr12:15482734
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-1240G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482734 | ||||||
| chr12:15482801
|
T | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-1173T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482801 | ||||||
| chr12:15482910
|
C | G | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.76-1064C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482910 | ||||||
| chr12:15482957
|
C | T | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1017C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482957 | ||||||
| chr12:15482963
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.76-1011G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15482963 | ||||||
| chr12:15483129
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-845C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15483129 | ||||||
| chr12:15483184
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-790A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15483184 | ||||||
| chr12:15483580
|
C | T | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-394C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15483580 | ||||||
| chr12:15483593
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-381A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15483593 | ||||||
| chr12:15483865
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-109A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 1/26 | chr12 | 15483865 | ||||||
| chr12:15484402
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+155C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484402 | ||||||
| chr12:15484458
|
C | A | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+211C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484458 | ||||||
| chr12:15484466
|
T | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.349+219T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484466 | ||||||
| chr12:15484489
|
T | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.349+242T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484489 | ||||||
| chr12:15484544
|
T | C | 1 | a0001c0003t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.349+297T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484544 | ||||||
| chr12:15484549
|
C | G | 1 | a0001c0003t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.349+302C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484549 | ||||||
| chr12:15484575
|
A | AT | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+335dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15484575 | |||||
| chr12:15484576
|
T | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(63): Show | 66 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.349+329T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484576 | ||||||
| chr12:15484586
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.349+339G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484586 | ||||||
| chr12:15484602
|
A | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(63): Show | 66 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.349+355A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484602 | ||||||
| chr12:15484657
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.349+410A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484657 | ||||||
| chr12:15484693
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.349+446G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484693 | ||||||
| chr12:15484946
|
A | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+699A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15484946 | ||||||
| chr12:15485237
|
C | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+990C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485237 | ||||||
| chr12:15485339
|
G | A | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.349+1092G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485339 | ||||||
| chr12:15485386
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349+1139A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485386 | ||||||
| chr12:15485657
|
C | T | 3 | a0001c0001t0001g0113a0001c0009t0001g0153a0001c0009t0001g0154 | 3 | HG00673.hp1 NA18946.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.349+1410C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485657 | ||||||
| chr12:15485758
|
A | C | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+1511A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485758 | ||||||
| chr12:15485833
|
T | C | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+1586T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485833 | ||||||
| chr12:15485847
|
G | C | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+1600G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485847 | ||||||
| chr12:15485849
|
G | C | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.349+1602G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485849 | ||||||
| chr12:15485913
|
T | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+1666T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15485913 | ||||||
| chr12:15486153
|
C | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.349+1906C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15486153 | ||||||
| chr12:15486293
|
C | A | 23 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(20): Show | 23 | HG00423.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.349+2046C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15486293 | ||||||
| chr12:15486537
|
A | G | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+2290A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15486537 | ||||||
| chr12:15486600
|
T | A | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349+2353T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15486600 | ||||||
| chr12:15486742
|
C | A | 1 | a0001c0001t0001g0010 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.349+2495C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15486742 | ||||||
| chr12:15486983
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.349+2736C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15486983 | ||||||
| chr12:15487091
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+2844C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487091 | ||||||
| chr12:15487110
|
G | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+2863G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487110 | ||||||
| chr12:15487229
|
A | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.349+2982A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487229 | ||||||
| chr12:15487387
|
G | A | 2 | a0001c0002t0003g0072a0001c0003t0001g0067 | 2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.349+3140G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487387 | ||||||
| chr12:15487552
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+3305C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487552 | ||||||
| chr12:15487620
|
TA | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+3374delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487620 | ||||||
| chr12:15487786
|
A | G | 1 | a0001c0005t0005g0096 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.349+3539A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487786 | ||||||
| chr12:15487791
|
T | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.349+3544T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487791 | ||||||
| chr12:15487866
|
C | A | 3 | a0001c0001t0003g0060a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG01884.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.349+3619C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15487866 | ||||||
| chr12:15488068
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 69 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.349+3821C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488068 | ||||||
| chr12:15488084
|
G | C | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349+3837G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488084 | ||||||
| chr12:15488196
|
C | T | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+3949C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488196 | ||||||
| chr12:15488418
|
A | G | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.349+4171A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488418 | ||||||
| chr12:15488658
|
G | A | 1 | a0001c0002t0001g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.349+4411G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488658 | ||||||
| chr12:15488740
|
G | A | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+4493G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488740 | ||||||
| chr12:15488897
|
G | A | 18 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(15): Show | 18 | HG00597.hp2 HG01074.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+4650G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488897 | ||||||
| chr12:15488898
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(4): Show | 7 | HG02074.hp1 NA18942.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+4651A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488898 | ||||||
| chr12:15488939
|
T | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+4692T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15488939 | ||||||
| chr12:15489008
|
A | G | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.349+4761A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489008 | ||||||
| chr12:15489009
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.349+4762G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489009 | ||||||
| chr12:15489069
|
A | T | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.349+4822A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489069 | ||||||
| chr12:15489291
|
G | A | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.349+5044G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489291 | ||||||
| chr12:15489313
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+5066G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489313 | ||||||
| chr12:15489602
|
G | C | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+5355G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489602 | ||||||
| chr12:15489920
|
G | C | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.349+5673G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489920 | ||||||
| chr12:15489921
|
T | A | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+5674T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15489921 | ||||||
| chr12:15490000
|
C | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 69 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.349+5753C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490000 | ||||||
| chr12:15490232
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.349+5985T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490232 | ||||||
| chr12:15490243
|
T | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.349+5996T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490243 | ||||||
| chr12:15490268
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.349+6021A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490268 | ||||||
| chr12:15490700
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+6453C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490700 | ||||||
| chr12:15490806
|
T | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350-6439T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490806 | ||||||
| chr12:15490866
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.350-6379G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490866 | ||||||
| chr12:15490884
|
G | A | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.350-6361G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490884 | ||||||
| chr12:15490940
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.350-6305G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15490940 | ||||||
| chr12:15491053
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.350-6192G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491053 | ||||||
| chr12:15491119
|
G | C | 14 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(11): Show | 14 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-6126G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491119 | ||||||
| chr12:15491130
|
C | A | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.350-6115C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491130 | ||||||
| chr12:15491130
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0101others(16): Show | 19 | HG01123.hp1 HG01123.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.350-6115C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491130 | ||||||
| chr12:15491328
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.350-5917C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491328 | ||||||
| chr12:15491355
|
T | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350-5890T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491355 | ||||||
| chr12:15491586
|
T | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-5659T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491586 | ||||||
| chr12:15491700
|
C | A | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-5545C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491700 | ||||||
| chr12:15491711
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.350-5534G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491711 | ||||||
| chr12:15491718
|
C | A | 23 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(20): Show | 23 | HG00423.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.350-5527C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15491718 | ||||||
| chr12:15491939
|
G | GACAA | 7 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-5280_350-5277d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15491939 | |||||
| chr12:15491939
|
GACAAACA others(1): Show |
G | 23 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(20): Show | 23 | HG00423.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.350-5284_350-5277d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15491939 | |||||
| chr12:15491961
|
CA | C | 6 | a0001c0001t0003g0030a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-5281delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15491961 | |||||
| chr12:15492079
|
A | G | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-5166A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492079 | ||||||
| chr12:15492408
|
A | C | 1 | a0001c0004t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.350-4837A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492408 | ||||||
| chr12:15492414
|
A | G | 8 | a0001c0001t0001g0078a0001c0002t0001g0077a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-4831A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492414 | ||||||
| chr12:15492530
|
T | A | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-4715T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492530 | ||||||
| chr12:15492622
|
T | G | 1 | a0001c0003t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.350-4623T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492622 | ||||||
| chr12:15492807
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350-4438G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492807 | ||||||
| chr12:15492875
|
A | G | 1 | a0001c0012t0006g0070 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.350-4370A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492875 | ||||||
| chr12:15492938
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 65 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.350-4307C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15492938 | ||||||
| chr12:15493032
|
GTTA | G | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4208_350-4206d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15493032 | |||||
| chr12:15493082
|
G | C | 6 | a0001c0001t0003g0030a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-4163G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15493082 | ||||||
| chr12:15493318
|
TA | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-3925delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15493318 | |||||
| chr12:15493409
|
T | A | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-3836T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15493409 | ||||||
| chr12:15493547
|
A | T | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.350-3698A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15493547 | ||||||
| chr12:15493662
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.350-3583A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15493662 | ||||||
| chr12:15493981
|
T | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350-3264T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15493981 | ||||||
| chr12:15494068
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.350-3177A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494068 | ||||||
| chr12:15494172
|
G | A | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-3073G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494172 | ||||||
| chr12:15494333
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.350-2912G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494333 | ||||||
| chr12:15494384
|
T | C | 4 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0002t0016g0061others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-2861T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494384 | ||||||
| chr12:15494623
|
A | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-2622A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494623 | ||||||
| chr12:15494677
|
T | C | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-2568T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494677 | ||||||
| chr12:15494685
|
GA | G | 20 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(17): Show | 20 | HG00597.hp2 HG01074.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.350-2552delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15494685 | |||||
| chr12:15494853
|
A | G | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-2392A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494853 | ||||||
| chr12:15494924
|
T | C | 1 | a0001c0002t0003g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-2321T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15494924 | ||||||
| chr12:15495012
|
ACTT | A | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-2229_350-2227d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15495012 | |||||
| chr12:15495329
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.350-1916A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495329 | ||||||
| chr12:15495483
|
T | C | 23 | a0001c0001t0001g0021a0001c0001t0001g0091a0001c0001t0001g0122others(20): Show | 23 | HG00423.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.350-1762T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495483 | ||||||
| chr12:15495543
|
G | C | 14 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(11): Show | 14 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1702G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495543 | ||||||
| chr12:15495623
|
G | A | 1 | a0001c0002t0008g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.350-1622G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495623 | ||||||
| chr12:15495660
|
C | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.350-1585C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495660 | ||||||
| chr12:15495681
|
G | A | 1 | a0001c0001t0004g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-1564G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495681 | ||||||
| chr12:15495714
|
A | G | 1 | a0001c0004t0001g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.350-1531A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495714 | ||||||
| chr12:15495729
|
G | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149 | 3 | HG02145.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.350-1516G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495729 | ||||||
| chr12:15495907
|
G | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.350-1338G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495907 | ||||||
| chr12:15495933
|
T | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.350-1312T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15495933 | ||||||
| chr12:15496043
|
C | G | 25 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0049others(22): Show | 25 | HG00733.hp1 HG01884.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.350-1202C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496043 | ||||||
| chr12:15496081
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.350-1164G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496081 | ||||||
| chr12:15496140
|
TTG | T | 17 | a0001c0001t0001g0021a0001c0001t0001g0126a0001c0001t0001g0136others(14): Show | 17 | HG01074.hp1 HG01167.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.350-1103_350-1102d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15496140 | |||||
| chr12:15496141
|
TG | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0122a0001c0002t0001g0087others(3): Show | 6 | HG00423.hp1 HG01243.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1103delG | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496141 | ||||||
| chr12:15496142
|
GT | G | 20 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00597.hp2 HG00621.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.350-1081delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15496142 | |||||
| chr12:15496142
|
GTT | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.350-1082_350-1081d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15496142 | |||||
| chr12:15496142
|
GTTT | G | 7 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0007g0080others(4): Show | 7 | HG02630.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-1083_350-1081d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | 15496142 | |||||
| chr12:15496149
|
T | G | 8 | a0001c0001t0001g0078a0001c0002t0001g0077a0001c0002t0002g0062others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1096T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496149 | ||||||
| chr12:15496151
|
T | G | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.350-1094T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496151 | ||||||
| chr12:15496154
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0014g0001 | 3 | HG00735.hp1 HG01981.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.350-1091T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496154 | ||||||
| chr12:15496195
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.350-1050T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496195 | ||||||
| chr12:15496203
|
C | T | 7 | a0001c0001t0001g0078a0001c0002t0002g0062a0001c0002t0002g0063others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-1042C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496203 | ||||||
| chr12:15496288
|
G | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-957G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496288 | ||||||
| chr12:15496289
|
T | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.350-956T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496289 | ||||||
| chr12:15496674
|
G | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.350-571G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496674 | ||||||
| chr12:15496965
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.350-280T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 2/26 | chr12 | 15496965 | ||||||
| chr12:15497476
|
C | T | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.508+73C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15497476 | ||||||
| chr12:15498426
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.509-1016C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15498426 | ||||||
| chr12:15498431
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.509-1011G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15498431 | ||||||
| chr12:15498504
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509-938G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15498504 | ||||||
| chr12:15498636
|
A | C | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-806A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15498636 | ||||||
| chr12:15498678
|
C | CAG | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.509-763_509-762ins others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr12 | 15498678 | |||||
| chr12:15498758
|
T | C | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.509-684T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15498758 | ||||||
| chr12:15499210
|
T | G | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.509-232T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15499210 | ||||||
| chr12:15499286
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.509-156A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15499286 | ||||||
| chr12:15499396
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.509-46T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 3/26 | chr12 | 15499396 | ||||||
| chr12:15499702
|
AAT | A | 30 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.661+115_661+116del others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15499702 | |||||
| chr12:15499717
|
T | C | 6 | a0001c0001t0003g0030a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.661+123T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15499717 | ||||||
| chr12:15499878
|
T | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.661+284T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15499878 | ||||||
| chr12:15499933
|
T | G | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.661+339T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15499933 | ||||||
| chr12:15499955
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.661+361A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15499955 | ||||||
| chr12:15500079
|
A | ATGGG | 63 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(60): Show | 63 | HG00423.hp1 HG00733.hp1 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.661+489_661+492dup others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15500079 | |||||
| chr12:15500083
|
G | GTGGA | 2 | a0001c0001t0003g0060a0001c0006t0004g0123 | 2 | HG01884.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.661+526_661+529dup others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15500083 | |||||
| chr12:15500083
|
G | GTGGGTGG others(1): Show |
54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(51): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.661+492_661+493ins others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15500083 | |||||
| chr12:15500083
|
G | GTGGGTGG others(5): Show |
27 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(24): Show | 27 | HG00733.hp2 HG01123.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.661+492_661+493ins others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15500083 | |||||
| chr12:15500083
|
G | GTGGGTGG others(9): Show |
2 | a0001c0001t0001g0093a0001c0005t0002g0109 | 2 | HG00735.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.661+492_661+493ins others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15500083 | |||||
| chr12:15500083
|
GTGGA | G | 2 | a0001c0009t0001g0153a0001c0009t0001g0154 | 2 | NA18946.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.661+526_661+529del others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15500083 | |||||
| chr12:15500087
|
A | G | 5 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0002t0016g0061others(2): Show | 5 | HG02630.hp1 HG02683.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+493A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500087 | ||||||
| chr12:15500189
|
T | C | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.661+595T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500189 | ||||||
| chr12:15500240
|
A | C | 3 | a0001c0001t0003g0060a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG01884.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.661+646A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500240 | ||||||
| chr12:15500244
|
G | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.661+650G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500244 | ||||||
| chr12:15500303
|
A | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.661+709A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500303 | ||||||
| chr12:15500387
|
T | C | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+793T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500387 | ||||||
| chr12:15500403
|
A | G | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.661+809A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500403 | ||||||
| chr12:15500507
|
G | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.661+913G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500507 | ||||||
| chr12:15500601
|
CAAAG | C | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.661+1008_661+1011d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500601 | ||||||
| chr12:15500708
|
G | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.662-912G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500708 | ||||||
| chr12:15500709
|
G | A | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.662-911G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500709 | ||||||
| chr12:15500752
|
T | C | 8 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.662-868T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500752 | ||||||
| chr12:15500763
|
A | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 69 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.662-857A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500763 | ||||||
| chr12:15500766
|
A | T | 3 | a0001c0001t0003g0060a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG01884.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.662-854A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500766 | ||||||
| chr12:15500778
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.662-842T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500778 | ||||||
| chr12:15500814
|
C | A | 1 | a0001c0002t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.662-806C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15500814 | ||||||
| chr12:15501101
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.662-519G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15501101 | ||||||
| chr12:15501117
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.662-503G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15501117 | ||||||
| chr12:15501282
|
AT | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.662-331delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr12 | 15501282 | |||||
| chr12:15501455
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.662-165T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 4/26 | chr12 | 15501455 | ||||||
| chr12:15502092
|
A | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1105+29A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502092 | ||||||
| chr12:15502097
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1105+34T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502097 | ||||||
| chr12:15502187
|
G | T | 1 | a0001c0007t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1105+124G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502187 | ||||||
| chr12:15502223
|
T | G | 31 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0091others(28): Show | 31 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1105+160T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502223 | ||||||
| chr12:15502403
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.1105+340G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502403 | ||||||
| chr12:15502553
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1105+490C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502553 | ||||||
| chr12:15502672
|
C | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1105+609C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502672 | ||||||
| chr12:15502766
|
T | C | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1105+703T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502766 | ||||||
| chr12:15502956
|
T | C | 4 | a0001c0002t0001g0032a0001c0002t0002g0031a0001c0002t0003g0033others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105+893T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502956 | ||||||
| chr12:15502979
|
C | T | 3 | a0001c0001t0001g0042a0001c0002t0001g0039a0001c0006t0004g0045 | 3 | HG00597.hp1 NA18988.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1105+916C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15502979 | ||||||
| chr12:15503008
|
A | G | 25 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0049others(22): Show | 25 | HG00733.hp1 HG01884.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1106-900A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15503008 | ||||||
| chr12:15503021
|
C | A | 22 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0002g0069others(19): Show | 22 | HG00733.hp1 HG01884.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.1106-887C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15503021 | ||||||
| chr12:15503111
|
T | A | 2 | a0001c0001t0001g0101a0001c0006t0004g0123 | 2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1106-797T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15503111 | ||||||
| chr12:15503482
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1106-426G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15503482 | ||||||
| chr12:15503606
|
A | T | 1 | a0001c0002t0001g0117 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1106-302A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15503606 | ||||||
| chr12:15503646
|
A | G | 3 | a0001c0001t0003g0060a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG01884.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1106-262A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15503646 | ||||||
| chr12:15503898
|
T | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.1106-10T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 5/26 | chr12 | 15503898 | ||||||
| chr12:15504386
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1267+317G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15504386 | ||||||
| chr12:15504524
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1267+455G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15504524 | ||||||
| chr12:15504630
|
GC | G | 5 | a0001c0002t0001g0035a0001c0002t0003g0028a0001c0002t0008g0027others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1267+562delC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15504630 | ||||||
| chr12:15504917
|
T | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1267+848T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15504917 | ||||||
| chr12:15505162
|
C | T | 20 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0090others(17): Show | 20 | HG00597.hp2 HG01074.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1267+1093C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505162 | ||||||
| chr12:15505199
|
T | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1267+1130T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505199 | ||||||
| chr12:15505201
|
G | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1267+1132G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505201 | ||||||
| chr12:15505415
|
T | A | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1267+1346T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505415 | ||||||
| chr12:15505422
|
T | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1267+1353T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505422 | ||||||
| chr12:15505448
|
C | G | 1 | a0001c0006t0004g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1267+1379C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505448 | ||||||
| chr12:15505454
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1267+1385C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505454 | ||||||
| chr12:15505496
|
C | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.1267+1427C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505496 | ||||||
| chr12:15505734
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 147 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.1267+1665C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505734 | ||||||
| chr12:15505848
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1267+1779C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505848 | ||||||
| chr12:15505871
|
T | C | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1267+1802T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505871 | ||||||
| chr12:15505995
|
G | A | 11 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0113others(8): Show | 11 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1267+1926G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15505995 | ||||||
| chr12:15506090
|
C | T | 26 | a0001c0001t0001g0073a0001c0001t0001g0093a0001c0001t0001g0113others(23): Show | 26 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1267+2021C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506090 | ||||||
| chr12:15506172
|
A | G | 87 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0037others(84): Show | 87 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1267+2103A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506172 | ||||||
| chr12:15506192
|
A | G | 6 | a0001c0001t0003g0030a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267+2123A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506192 | ||||||
| chr12:15506370
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1268-2201A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506370 | ||||||
| chr12:15506433
|
A | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0126others(2): Show | 5 | HG00673.hp2 HG02132.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1268-2138A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506433 | ||||||
| chr12:15506556
|
G | A | 2 | a0001c0001t0001g0111a0001c0002t0001g0018 | 2 | HG01123.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1268-2015G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506556 | ||||||
| chr12:15506566
|
C | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(39): Show | 42 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1268-2005C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506566 | ||||||
| chr12:15506682
|
T | G | 2 | a0001c0002t0007g0080a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1268-1889T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15506682 | ||||||
| chr12:15507040
|
T | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.1268-1531T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507040 | ||||||
| chr12:15507105
|
C | A | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1268-1466C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507105 | ||||||
| chr12:15507273
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1268-1298C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507273 | ||||||
| chr12:15507314
|
G | A | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1268-1257G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507314 | ||||||
| chr12:15507410
|
A | AAAAT | 27 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0093others(24): Show | 27 | HG00597.hp1 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1268-1122_1268-111 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr12 | 15507410 | |||||
| chr12:15507410
|
AAAAT | A | 4 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0012g0084others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1268-1122_1268-111 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr12 | 15507410 | |||||
| chr12:15507410
|
AAAATAAA others(1): Show |
A | 12 | a0001c0001t0001g0078a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1268-1126_1268-111 others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr12 | 15507410 | |||||
| chr12:15507450
|
T | C | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1268-1121T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507450 | ||||||
| chr12:15507450
|
T | TAAATAAA others(4): Show |
19 | a0001c0001t0001g0042a0001c0001t0001g0091a0001c0001t0001g0125others(16): Show | 19 | HG00673.hp2 HG01516.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1268-1119_1268-111 others(15): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr12 | 15507450 | |||||
| chr12:15507450
|
T | TAAATAAC | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1268-1119_1268-111 others(11): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr12 | 15507450 | |||||
| chr12:15507450
|
T | TAAC | 6 | a0001c0001t0001g0073a0001c0001t0001g0130a0001c0001t0006g0068others(3): Show | 6 | HG01261.hp2 HG02300.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1268-1119_1268-111 others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr12 | 15507450 | |||||
| chr12:15507464
|
C | T | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1268-1107C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507464 | ||||||
| chr12:15507647
|
C | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1268-924C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507647 | ||||||
| chr12:15507733
|
C | A | 1 | a0001c0001t0004g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1268-838C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507733 | ||||||
| chr12:15507759
|
G | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(71): Show | 74 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1268-812G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15507759 | ||||||
| chr12:15508036
|
A | G | 74 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(71): Show | 74 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1268-535A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508036 | ||||||
| chr12:15508144
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1268-427T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508144 | ||||||
| chr12:15508205
|
A | G | 2 | a0001c0002t0007g0080a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1268-366A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508205 | ||||||
| chr12:15508229
|
G | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(50): Show | 53 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1268-342G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508229 | ||||||
| chr12:15508248
|
T | C | 41 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0078others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1268-323T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508248 | ||||||
| chr12:15508290
|
A | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(71): Show | 74 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1268-281A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508290 | ||||||
| chr12:15508308
|
A | G | 82 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(79): Show | 82 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1268-263A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508308 | ||||||
| chr12:15508340
|
G | A | 24 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(21): Show | 24 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1268-231G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508340 | ||||||
| chr12:15508507
|
A | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1268-64A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 6/26 | chr12 | 15508507 | ||||||
| chr12:15509036
|
T | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+269T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509036 | ||||||
| chr12:15509051
|
G | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+284G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509051 | ||||||
| chr12:15509136
|
G | A | 25 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1464+369G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509136 | ||||||
| chr12:15509363
|
G | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+596G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509363 | ||||||
| chr12:15509372
|
C | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+605C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509372 | ||||||
| chr12:15509374
|
G | GA | 6 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0001g0113others(3): Show | 6 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1464+621dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15509374 | |||||
| chr12:15509374
|
GA | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(58): Show | 61 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1464+621delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15509374 | |||||
| chr12:15509374
|
GAA | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+620_1464+621d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15509374 | |||||
| chr12:15509394
|
A | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0003t0001g0036 | 3 | HG01934.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1464+627A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509394 | ||||||
| chr12:15509431
|
T | A | 25 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1464+664T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509431 | ||||||
| chr12:15509446
|
C | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+679C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509446 | ||||||
| chr12:15509462
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1464+695C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509462 | ||||||
| chr12:15509467
|
C | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+700C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509467 | ||||||
| chr12:15509567
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1464+800C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509567 | ||||||
| chr12:15509568
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1464+801G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509568 | ||||||
| chr12:15509590
|
G | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+823G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509590 | ||||||
| chr12:15509644
|
C | CCGAGATC others(3): Show |
63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+878_1464+879i others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15509644 | |||||
| chr12:15509695
|
A | AAG | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+928_1464+929i others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509695 | ||||||
| chr12:15509696
|
G | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+929G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509696 | ||||||
| chr12:15509725
|
A | G | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1464+958A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509725 | ||||||
| chr12:15509835
|
T | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+1068T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509835 | ||||||
| chr12:15509859
|
G | A | 1 | a0001c0001t0006g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1464+1092G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509859 | ||||||
| chr12:15509871
|
A | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(88): Show | 91 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1464+1104A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509871 | ||||||
| chr12:15509888
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(88): Show | 91 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1464+1121T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509888 | ||||||
| chr12:15509916
|
G | C | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+1149G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509916 | ||||||
| chr12:15509962
|
A | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+1195A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15509962 | ||||||
| chr12:15510051
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+1284A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510051 | ||||||
| chr12:15510065
|
T | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(89): Show | 92 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.1464+1298T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510065 | ||||||
| chr12:15510131
|
T | A | 15 | a0001c0001t0001g0078a0001c0002t0001g0032a0001c0002t0001g0077others(12): Show | 15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1464+1364T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510131 | ||||||
| chr12:15510304
|
C | T | 6 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(3): Show | 6 | HG00597.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1464+1537C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510304 | ||||||
| chr12:15510502
|
A | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(88): Show | 91 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1464+1735A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510502 | ||||||
| chr12:15510521
|
T | C | 25 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1464+1754T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510521 | ||||||
| chr12:15510618
|
G | A | 33 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(30): Show | 33 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1464+1851G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510618 | ||||||
| chr12:15510655
|
A | G | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1464+1888A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510655 | ||||||
| chr12:15510843
|
C | T | 2 | a0001c0002t0004g0034a0001c0002t0004g0163 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1464+2076C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510843 | ||||||
| chr12:15510984
|
T | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+2217T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510984 | ||||||
| chr12:15510988
|
G | A | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1464+2221G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15510988 | ||||||
| chr12:15511003
|
C | CA | 5 | a0001c0001t0001g0020a0001c0001t0001g0104a0001c0003t0001g0089others(2): Show | 5 | HG00423.hp2 HG00621.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464+2255dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15511003 | |||||
| chr12:15511003
|
C | CAAAAA | 28 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(25): Show | 28 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1464+2251_1464+225 others(9): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15511003 | |||||
| chr12:15511003
|
C | CAAAAAA | 16 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0037others(13): Show | 16 | HG01515.hp1 HG01884.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1464+2250_1464+225 others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15511003 | |||||
| chr12:15511003
|
C | CAAAAAAA | 15 | a0001c0001t0001g0021a0001c0001t0001g0119a0001c0001t0001g0148others(12): Show | 15 | HG00597.hp1 HG01074.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1464+2249_1464+225 others(11): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15511003 | |||||
| chr12:15511003
|
CAA | C | 16 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0002t0001g0032others(13): Show | 16 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1464+2254_1464+225 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15511003 | |||||
| chr12:15511003
|
CAAA | C | 12 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0001g0136others(9): Show | 12 | HG00733.hp2 HG01261.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1464+2253_1464+225 others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15511003 | |||||
| chr12:15511034
|
G | A | 100 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(97): Show | 100 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1464+2267G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511034 | ||||||
| chr12:15511253
|
T | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+2486T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511253 | ||||||
| chr12:15511289
|
C | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+2522C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511289 | ||||||
| chr12:15511573
|
T | C | 2 | a0001c0004t0001g0099a0001c0004t0001g0100 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1464+2806T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511573 | ||||||
| chr12:15511634
|
T | C | 100 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(97): Show | 100 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1464+2867T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511634 | ||||||
| chr12:15511652
|
G | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+2885G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511652 | ||||||
| chr12:15511666
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+2899A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511666 | ||||||
| chr12:15511766
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+2999A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511766 | ||||||
| chr12:15511921
|
A | T | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1464+3154A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511921 | ||||||
| chr12:15511929
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1464+3162A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511929 | ||||||
| chr12:15511978
|
C | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1464+3211C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15511978 | ||||||
| chr12:15512094
|
G | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1464+3327G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512094 | ||||||
| chr12:15512099
|
G | GT | 32 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(29): Show | 32 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1464+3339dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15512099 | |||||
| chr12:15512107
|
G | T | 49 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(46): Show | 49 | HG00423.hp1 HG00735.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.1464+3340G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512107 | ||||||
| chr12:15512127
|
G | T | 98 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(95): Show | 98 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1464+3360G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512127 | ||||||
| chr12:15512158
|
A | C | 4 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0002t0016g0061others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-3340A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512158 | ||||||
| chr12:15512347
|
T | C | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1465-3151T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512347 | ||||||
| chr12:15512458
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(88): Show | 91 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1465-3040G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512458 | ||||||
| chr12:15512544
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(88): Show | 91 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1465-2954A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512544 | ||||||
| chr12:15512675
|
C | T | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1465-2823C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512675 | ||||||
| chr12:15512860
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(27): Show | 30 | HG00597.hp1 HG01074.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1465-2638G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512860 | ||||||
| chr12:15512911
|
G | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(88): Show | 91 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1465-2587G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15512911 | ||||||
| chr12:15513071
|
GGAAAGAA others(1): Show |
G | 10 | a0001c0001t0001g0037a0001c0001t0001g0138a0001c0001t0001g0148others(7): Show | 10 | HG00597.hp1 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1465-2411_1465-240 others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513071 | |||||
| chr12:15513083
|
AGAAAGAA others(45): Show |
A | 6 | a0001c0002t0001g0019a0001c0002t0001g0137a0001c0002t0001g0155others(3): Show | 6 | HG01981.hp1 HG02683.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-2411_1465-236 others(56): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513083 | |||||
| chr12:15513083
|
AGAAAGAA others(49): Show |
A | 2 | a0001c0002t0001g0035a0001c0008t0004g0071 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1465-2411_1465-235 others(60): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513083 | |||||
| chr12:15513084
|
GA | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1465-2411delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513084 | |||||
| chr12:15513084
|
GAAAGAAA others(67): Show |
G | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1465-2411_1465-233 others(78): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513084 | |||||
| chr12:15513084
|
GAAAGAAA others(71): Show |
G | 25 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1465-2411_1465-233 others(82): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513084 | |||||
| chr12:15513089
|
AAAG | A | 2 | a0001c0001t0001g0029a0001c0002t0002g0131 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1465-2403_1465-240 others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513089 | |||||
| chr12:15513091
|
A | G | 2 | a0001c0004t0001g0099a0001c0004t0001g0100 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1465-2407A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513091 | ||||||
| chr12:15513092
|
G | A | 2 | a0001c0004t0001g0099a0001c0004t0001g0100 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1465-2406G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513092 | ||||||
| chr12:15513092
|
G | GA | 11 | a0001c0001t0001g0078a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1465-2404dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513092 | |||||
| chr12:15513092
|
GAAGAAAG others(58): Show |
G | 2 | a0001c0002t0007g0080a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1465-2403_1465-233 others(69): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513092 | |||||
| chr12:15513093
|
AAGAAAGA others(40): Show |
A | 14 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0119others(11): Show | 14 | HG01123.hp1 HG01167.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1465-2403_1465-235 others(51): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513093 | |||||
| chr12:15513095
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0110others(19): Show | 22 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1465-2403G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513095 | ||||||
| chr12:15513096
|
A | G | 22 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0110others(19): Show | 22 | HG00621.hp2 HG00673.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1465-2402A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513096 | ||||||
| chr12:15513099
|
GA | G | 8 | a0001c0001t0001g0078a0001c0002t0002g0062a0001c0002t0002g0063others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1465-2396delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513099 | |||||
| chr12:15513103
|
GA | G | 2 | a0001c0002t0002g0064a0001c0002t0002g0131 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1465-2392delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513103 | |||||
| chr12:15513104
|
AAAGAAAG others(5): Show |
A | 1 | a0001c0001t0001g0090 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1465-2390_1465-237 others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513104 | |||||
| chr12:15513106
|
A | T | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1465-2392A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513106 | ||||||
| chr12:15513108
|
AAAGG | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0120others(8): Show | 11 | HG01074.hp2 HG01243.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1465-2358_1465-235 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513108 | |||||
| chr12:15513108
|
AAAGGAAG others(1): Show |
A | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(23): Show | 26 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1465-2362_1465-235 others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513108 | |||||
| chr12:15513108
|
AAAGGAAG others(5): Show |
A | 8 | a0001c0002t0003g0072a0001c0002t0006g0058a0001c0002t0006g0162others(5): Show | 8 | HG02451.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1465-2366_1465-235 others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513108 | |||||
| chr12:15513108
|
AAAGGAAG others(25): Show |
A | 10 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0138others(7): Show | 10 | HG00597.hp1 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1465-2386_1465-235 others(36): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513108 | |||||
| chr12:15513110
|
AGGAAGGA others(22): Show |
A | 1 | a0001c0002t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1465-2386_1465-235 others(33): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513110 | |||||
| chr12:15513111
|
GGAAGGAA others(39): Show |
G | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1465-2386_1465-234 others(50): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513111 | ||||||
| chr12:15513112
|
G | A | 20 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0101others(17): Show | 20 | HG00621.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1465-2386G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513112 | ||||||
| chr12:15513116
|
G | A | 6 | a0001c0001t0001g0088a0001c0002t0002g0050a0001c0002t0002g0064others(3): Show | 6 | HG03209.hp1 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-2382G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513116 | ||||||
| chr12:15513120
|
G | A | 2 | a0001c0001t0001g0113a0001c0002t0004g0163 | 2 | HG00673.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1465-2378G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513120 | ||||||
| chr12:15513124
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1465-2374G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513124 | ||||||
| chr12:15513128
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1465-2370G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513128 | ||||||
| chr12:15513132
|
GAAGGAAG others(5): Show |
G | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1465-2362_1465-235 others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513132 | |||||
| chr12:15513132
|
GAAGGAAG others(23): Show |
G | 1 | a0001c0003t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1465-2362_1465-233 others(34): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513132 | |||||
| chr12:15513136
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0091others(6): Show | 9 | HG02257.hp1 HG02738.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.1465-2362G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513136 | ||||||
| chr12:15513136
|
GAAGGAAG others(15): Show |
G | 1 | a0001c0002t0002g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1465-2358_1465-233 others(26): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513136 | |||||
| chr12:15513136
|
GAAGGAAG others(19): Show |
G | 2 | a0001c0001t0001g0078a0001c0002t0003g0079 | 2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1465-2358_1465-233 others(30): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513136 | |||||
| chr12:15513139
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1465-2359G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513139 | ||||||
| chr12:15513139
|
G | GAAAGAAA others(3): Show |
1 | a0001c0001t0010g0022 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1465-2359_1465-235 others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513139 | ||||||
| chr12:15513139
|
GGAAGAAA others(11): Show |
G | 1 | a0001c0002t0002g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1465-2358_1465-234 others(22): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513139 | ||||||
| chr12:15513140
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0016others(34): Show | 37 | HG00621.hp2 HG00673.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1465-2358G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513140 | ||||||
| chr12:15513140
|
GAAGAAAG others(11): Show |
G | 1 | a0001c0002t0002g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1465-2339_1465-232 others(22): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513140 | |||||
| chr12:15513140
|
GAAGAAAG others(15): Show |
G | 1 | a0001c0002t0003g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1465-2339_1465-231 others(26): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513140 | |||||
| chr12:15513140
|
GAAGAAAG others(19): Show |
G | 2 | a0001c0001t0001g0042a0001c0002t0002g0064 | 2 | HG03209.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1465-2339_1465-231 others(30): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513140 | |||||
| chr12:15513143
|
GAAAGAAA others(7): Show |
G | 4 | a0001c0001t0006g0068a0001c0002t0002g0063a0001c0002t0003g0057others(1): Show | 4 | HG01261.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1465-2339_1465-232 others(18): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513143 | |||||
| chr12:15513144
|
A | G | 3 | a0001c0001t0001g0110a0001c0002t0001g0039a0001c0002t0004g0163 | 3 | HG03486.hp1 NA18942.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1465-2354A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513144 | ||||||
| chr12:15513144
|
AAAGAAAG others(4): Show |
A | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1465-2351_1465-234 others(15): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513144 | |||||
| chr12:15513146
|
A | T | 3 | a0001c0001t0001g0029a0001c0002t0008g0027a0001c0003t0001g0026 | 3 | HG02559.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1465-2352A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513146 | ||||||
| chr12:15513147
|
GAAAGAAA others(3): Show |
G | 4 | a0001c0001t0001g0136a0001c0002t0003g0143a0001c0005t0002g0109others(1): Show | 4 | HG00733.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-2339_1465-233 others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513147 | |||||
| chr12:15513148
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1465-2350A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513148 | ||||||
| chr12:15513150
|
A | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0138a0001c0001t0001g0148others(5): Show | 8 | HG00597.hp1 HG01074.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1465-2348A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513150 | ||||||
| chr12:15513151
|
G | A | 2 | a0001c0003t0001g0038a0001c0006t0004g0152 | 2 | NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1465-2347G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513151 | ||||||
| chr12:15513151
|
GAAAGAA | G | 9 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0003g0030others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-2339_1465-233 others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513151 | |||||
| chr12:15513152
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1465-2346A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513152 | ||||||
| chr12:15513153
|
A | G | 2 | a0001c0003t0001g0038a0001c0006t0004g0152 | 2 | NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1465-2345A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513153 | ||||||
| chr12:15513153
|
AAGAAAAA others(1): Show |
A | 4 | a0001c0001t0009g0015a0001c0001t0009g0048a0001c0002t0002g0076others(1): Show | 4 | HG00673.hp2 HG02132.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-2343_1465-233 others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513153 | |||||
| chr12:15513153
|
AAGAAAAA others(5): Show |
A | 2 | a0001c0002t0004g0034a0001c0003t0001g0089 | 2 | HG01261.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1465-2343_1465-233 others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513153 | |||||
| chr12:15513153
|
AAGAAAAA others(9): Show |
A | 1 | a0001c0002t0002g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1465-2343_1465-232 others(20): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513153 | |||||
| chr12:15513155
|
G | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0073a0001c0001t0001g0120others(11): Show | 14 | HG00733.hp1 HG01074.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1465-2343G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513155 | ||||||
| chr12:15513155
|
GAA | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0029others(25): Show | 28 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1465-2339_1465-233 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513155 | |||||
| chr12:15513157
|
A | AAG | 7 | a0001c0001t0001g0122a0001c0001t0010g0022a0001c0001t0010g0023others(4): Show | 7 | HG00621.hp2 HG02055.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1465-2340_1465-233 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513157 | |||||
| chr12:15513157
|
A | ATG | 9 | a0001c0001t0001g0021a0001c0001t0001g0119a0001c0001t0001g0156others(6): Show | 9 | HG01123.hp1 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1465-2341_1465-234 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513157 | ||||||
| chr12:15513157
|
A | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0073a0001c0001t0001g0120others(14): Show | 17 | HG00733.hp1 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1465-2341A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513157 | ||||||
| chr12:15513157
|
AAAAG | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0113others(8): Show | 11 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1465-2273_1465-227 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513157 | |||||
| chr12:15513157
|
AAAAGAAA others(1): Show |
A | 6 | a0001c0001t0001g0044a0001c0003t0001g0074a0001c0003t0001g0106others(3): Show | 6 | HG00423.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-2277_1465-227 others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513157 | |||||
| chr12:15513157
|
AAAAGAAA others(5): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1465-2281_1465-227 others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513157 | |||||
| chr12:15513158
|
A | G | 2 | a0001c0001t0006g0068a0001c0002t0002g0063 | 2 | HG01261.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1465-2340A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513158 | ||||||
| chr12:15513160
|
A | T | 6 | a0001c0001t0001g0006a0001c0001t0007g0083a0001c0001t0007g0085others(3): Show | 6 | HG01167.hp2 HG01515.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-2338A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513160 | ||||||
| chr12:15513162
|
A | G | 1 | a0001c0002t0002g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1465-2336A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513162 | ||||||
| chr12:15513164
|
A | T | 5 | a0001c0002t0001g0019a0001c0002t0001g0137a0001c0002t0001g0155others(2): Show | 5 | HG01981.hp1 HG02683.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-2334A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513164 | ||||||
| chr12:15513168
|
A | T | 2 | a0001c0002t0001g0035a0001c0008t0004g0071 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1465-2330A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513168 | ||||||
| chr12:15513170
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1465-2328A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513170 | ||||||
| chr12:15513172
|
A | T | 2 | a0001c0002t0007g0080a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1465-2326A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513172 | ||||||
| chr12:15513180
|
A | T | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1465-2318A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513180 | ||||||
| chr12:15513184
|
A | T | 25 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1465-2314A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513184 | ||||||
| chr12:15513202
|
A | G | 1 | a0001c0002t0008g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1465-2296A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513202 | ||||||
| chr12:15513205
|
GAA | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1465-2291_1465-229 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513205 | |||||
| chr12:15513206
|
A | G | 31 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(28): Show | 31 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1465-2292A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513206 | ||||||
| chr12:15513210
|
A | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1465-2288A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513210 | ||||||
| chr12:15513214
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1465-2284A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513214 | ||||||
| chr12:15513222
|
A | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1465-2276A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513222 | ||||||
| chr12:15513226
|
A | G | 28 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0110others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1465-2272A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513226 | ||||||
| chr12:15513282
|
GGGAA | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1465-2197_1465-219 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15513282 | |||||
| chr12:15513286
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1465-2212A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513286 | ||||||
| chr12:15513520
|
T | C | 25 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1465-1978T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513520 | ||||||
| chr12:15513583
|
C | T | 97 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(94): Show | 97 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1465-1915C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513583 | ||||||
| chr12:15513708
|
G | A | 27 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0134others(24): Show | 27 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1465-1790G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513708 | ||||||
| chr12:15513947
|
T | C | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1465-1551T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15513947 | ||||||
| chr12:15514033
|
C | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1465-1465C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514033 | ||||||
| chr12:15514116
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1465-1382T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514116 | ||||||
| chr12:15514170
|
G | A | 17 | a0001c0001t0001g0093a0001c0001t0005g0102a0001c0001t0005g0103others(14): Show | 17 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1465-1328G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514170 | ||||||
| chr12:15514444
|
T | A | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1465-1054T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514444 | ||||||
| chr12:15514451
|
C | CA | 21 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0005g0102others(18): Show | 21 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1465-1025dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15514451 | |||||
| chr12:15514451
|
CA | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0134others(6): Show | 9 | HG01261.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-1025delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr12 | 15514451 | |||||
| chr12:15514464
|
A | G | 6 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0001g0136others(3): Show | 6 | HG01261.hp2 HG02258.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-1034A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514464 | ||||||
| chr12:15514468
|
A | G | 6 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0001g0136others(3): Show | 6 | HG01261.hp2 HG02258.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-1030A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514468 | ||||||
| chr12:15514469
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0119others(16): Show | 19 | HG00597.hp1 HG01074.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1465-1029A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514469 | ||||||
| chr12:15514471
|
A | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0001g0136others(3): Show | 6 | HG01261.hp2 HG02258.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-1027A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514471 | ||||||
| chr12:15514473
|
A | AAAGAAAG others(5): Show |
4 | a0001c0002t0002g0031a0001c0002t0002g0064a0001c0005t0002g0109others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1465-1025_1465-102 others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514473 | ||||||
| chr12:15514473
|
A | AAGAAAGA others(4): Show |
17 | a0001c0001t0001g0078a0001c0001t0003g0030a0001c0002t0001g0032others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1465-1025_1465-102 others(15): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514473 | ||||||
| chr12:15514473
|
A | G | 6 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0001g0136others(3): Show | 6 | HG01261.hp2 HG02258.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-1025A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514473 | ||||||
| chr12:15514474
|
G | T | 27 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0134others(24): Show | 27 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1465-1024G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514474 | ||||||
| chr12:15514908
|
A | C | 1 | a0001c0007t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1465-590A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15514908 | ||||||
| chr12:15515043
|
G | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(60): Show | 63 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1465-455G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15515043 | ||||||
| chr12:15515129
|
C | T | 97 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(94): Show | 97 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1465-369C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15515129 | ||||||
| chr12:15515218
|
G | A | 25 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0128others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1465-280G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15515218 | ||||||
| chr12:15515329
|
C | T | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1465-169C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15515329 | ||||||
| chr12:15515366
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1465-132G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15515366 | ||||||
| chr12:15515403
|
G | T | 2 | a0001c0004t0001g0099a0001c0004t0001g0100 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1465-95G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 7/26 | chr12 | 15515403 | ||||||
| chr12:15515645
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1585+27A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515645 | ||||||
| chr12:15515707
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1585+89C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515707 | ||||||
| chr12:15515708
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1585+90G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515708 | ||||||
| chr12:15515834
|
T | G | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1585+216T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515834 | ||||||
| chr12:15515987
|
G | GT | 38 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(35): Show | 38 | HG00597.hp1 HG00621.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1585+373dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15515987 | |||||
| chr12:15515987
|
G | GTT | 10 | a0001c0001t0001g0010a0001c0001t0001g0073a0001c0001t0001g0113others(7): Show | 10 | HG00423.hp2 HG00597.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1585+372_1585+373d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15515987 | |||||
| chr12:15515987
|
G | T | 20 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0134others(17): Show | 20 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1585+369G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515987 | ||||||
| chr12:15515988
|
T | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1585+370T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515988 | ||||||
| chr12:15515988
|
T | TG | 19 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0134others(16): Show | 19 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1585+370_1585+371i others(3): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515988 | ||||||
| chr12:15515991
|
TG | T | 6 | a0001c0002t0012g0084a0001c0003t0001g0074a0001c0004t0001g0099others(3): Show | 6 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1585+374delG | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515991 | ||||||
| chr12:15515992
|
G | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.1585+374G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515992 | ||||||
| chr12:15515994
|
T | G | 2 | a0001c0001t0001g0042a0001c0002t0002g0065 | 2 | HG01109.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1585+376T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515994 | ||||||
| chr12:15515995
|
T | G | 19 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0134others(16): Show | 19 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1585+377T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15515995 | ||||||
| chr12:15516059
|
C | T | 1 | a0001c0012t0006g0070 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1585+441C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516059 | ||||||
| chr12:15516103
|
G | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0002t0001g0013others(7): Show | 10 | HG01515.hp1 HG01516.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1585+485G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516103 | ||||||
| chr12:15516179
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0138others(17): Show | 20 | HG00733.hp2 HG01123.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1585+561A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516179 | ||||||
| chr12:15516212
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1586-551G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516212 | ||||||
| chr12:15516378
|
C | T | 10 | a0001c0001t0001g0111a0001c0001t0001g0128a0001c0002t0001g0008others(7): Show | 10 | HG01123.hp2 HG01516.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1586-385C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516378 | ||||||
| chr12:15516433
|
AAAGAGAG others(8): Show |
A | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(40): Show | 43 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1586-313_1586-299d others(17): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516433 | |||||
| chr12:15516479
|
AAGAG | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0138others(24): Show | 27 | HG00733.hp2 HG01123.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1586-278_1586-275d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516479 | |||||
| chr12:15516517
|
GA | G | 3 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0002t0016g0061 | 3 | HG02630.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1586-241delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516517 | |||||
| chr12:15516518
|
A | AAAAAG | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1586-233_1586-229d others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516518 | |||||
| chr12:15516518
|
A | AAAAAGAA others(3): Show |
5 | a0001c0001t0001g0113a0001c0003t0001g0124a0001c0006t0004g0114others(2): Show | 5 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.1586-238_1586-229d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516518 | |||||
| chr12:15516563
|
G | A | 10 | a0001c0001t0001g0078a0001c0002t0002g0062a0001c0002t0002g0063others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1586-200G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516563 | ||||||
| chr12:15516606
|
A | AAAGGGAG others(1): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1586-152_1586-145d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516606 | |||||
| chr12:15516606
|
A | AAAGGGAG others(9): Show |
1 | a0001c0002t0003g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1586-145_1586-144i others(18): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516606 | |||||
| chr12:15516611
|
G | GAGGAAGG others(5): Show |
6 | a0001c0002t0001g0032a0001c0002t0001g0077a0001c0002t0002g0031others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1586-145_1586-144i others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516611 | |||||
| chr12:15516615
|
A | AAGGG | 25 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0037others(22): Show | 25 | HG01074.hp2 HG01123.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.1586-145_1586-144i others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516615 | |||||
| chr12:15516619
|
A | G | 86 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0073others(83): Show | 86 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1586-144A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516619 | ||||||
| chr12:15516627
|
A | G | 8 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0064others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1586-136A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516627 | ||||||
| chr12:15516631
|
A | G | 15 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0088others(12): Show | 15 | HG01123.hp2 HG01516.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1586-132A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516631 | ||||||
| chr12:15516635
|
A | AAGGAAGG others(13): Show |
8 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0064others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1586-125_1586-124i others(22): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516635 | |||||
| chr12:15516635
|
A | AAGGGAGG others(1): Show |
5 | a0001c0002t0012g0084a0001c0004t0001g0099a0001c0004t0001g0100others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1586-120_1586-113d others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516635 | |||||
| chr12:15516635
|
A | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(53): Show | 56 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1586-128A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516635 | ||||||
| chr12:15516639
|
G | A | 6 | a0001c0001t0001g0113a0001c0002t0004g0056a0001c0002t0011g0082others(3): Show | 6 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1586-124G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516639 | ||||||
| chr12:15516647
|
GAGGT | G | 27 | a0001c0001t0001g0006a0001c0002t0001g0032a0001c0002t0001g0077others(24): Show | 27 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1586-110_1586-107d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr12 | 15516647 | |||||
| chr12:15516651
|
T | G | 15 | a0001c0001t0001g0093a0001c0002t0001g0008a0001c0002t0004g0056others(12): Show | 15 | HG00423.hp1 HG00735.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1586-112T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 8/26 | chr12 | 15516651 | ||||||
| chr12:15517246
|
A | C | 68 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(65): Show | 68 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(65): Show |
intron_variant | MODIFIER | c.1779+290A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15517246 | ||||||
| chr12:15517254
|
T | C | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.1779+298T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15517254 | ||||||
| chr12:15517316
|
C | T | 3 | a0001c0002t0006g0058a0001c0002t0006g0059a0001c0002t0006g0162 | 3 | HG02109.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1779+360C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15517316 | ||||||
| chr12:15517373
|
A | G | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1779+417A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15517373 | ||||||
| chr12:15517822
|
A | G | 78 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(75): Show | 78 | HG00423.hp2 HG00597.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1779+866A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15517822 | ||||||
| chr12:15517946
|
G | A | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1779+990G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15517946 | ||||||
| chr12:15517976
|
G | A | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.1779+1020G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15517976 | ||||||
| chr12:15518019
|
T | TC | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.1779+1065dupC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr12 | 15518019 | |||||
| chr12:15518031
|
G | GC | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.1779+1077dupC | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr12 | 15518031 | |||||
| chr12:15518059
|
C | G | 1 | a0001c0002t0003g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1779+1103C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15518059 | ||||||
| chr12:15518119
|
G | A | 3 | a0001c0002t0004g0034a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1779+1163G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15518119 | ||||||
| chr12:15518142
|
C | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1779+1186C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15518142 | ||||||
| chr12:15518185
|
GCCAAGCC others(25): Show |
G | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1779+1265_1779+129 others(36): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr12 | 15518185 | |||||
| chr12:15518198
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1779+1242G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15518198 | ||||||
| chr12:15518342
|
C | A | 70 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(67): Show | 70 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(67): Show |
intron_variant | MODIFIER | c.1779+1386C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15518342 | ||||||
| chr12:15518426
|
G | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1779+1470G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15518426 | ||||||
| chr12:15519000
|
C | T | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1780-1201C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15519000 | ||||||
| chr12:15519048
|
A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0088others(4): Show | 7 | HG00735.hp2 HG01074.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1780-1153A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15519048 | ||||||
| chr12:15519136
|
G | A | 78 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(75): Show | 78 | HG00423.hp2 HG00597.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1780-1065G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15519136 | ||||||
| chr12:15519340
|
G | T | 1 | a0001c0001t0006g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1780-861G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15519340 | ||||||
| chr12:15519454
|
A | G | 2 | a0001c0002t0004g0163a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1780-747A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15519454 | ||||||
| chr12:15519710
|
A | G | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1780-491A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15519710 | ||||||
| chr12:15519851
|
G | A | 68 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(65): Show | 68 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(65): Show |
intron_variant | MODIFIER | c.1780-350G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15519851 | ||||||
| chr12:15520034
|
A | G | 1 | a0001c0008t0004g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1780-167A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15520034 | ||||||
| chr12:15520045
|
G | A | 1 | a0001c0006t0004g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1780-156G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15520045 | ||||||
| chr12:15520169
|
C | T | 24 | a0001c0002t0001g0018a0001c0002t0003g0028a0001c0002t0004g0056others(21): Show | 24 | HG01123.hp2 HG01169.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1780-32C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 9/26 | chr12 | 15520169 | ||||||
| chr12:15520769
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(159): Show |
intron_variant | MODIFIER | c.1891+457G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15520769 | ||||||
| chr12:15520821
|
G | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1891+509G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15520821 | ||||||
| chr12:15520833
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1891+521A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15520833 | ||||||
| chr12:15520898
|
T | C | 1 | a0001c0004t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1891+586T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15520898 | ||||||
| chr12:15521003
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1891+691T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521003 | ||||||
| chr12:15521036
|
A | C | 35 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0019others(32): Show | 35 | HG00733.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1891+724A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521036 | ||||||
| chr12:15521106
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891+794A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521106 | ||||||
| chr12:15521116
|
T | C | 2 | a0001c0001t0007g0083a0001c0001t0007g0085 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1891+804T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521116 | ||||||
| chr12:15521166
|
GAATAATT others(29): Show |
G | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1891+856_1891+891d others(38): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 15521166 | |||||
| chr12:15521341
|
G | T | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.1891+1029G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521341 | ||||||
| chr12:15521367
|
C | G | 74 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(71): Show | 74 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.1891+1055C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521367 | ||||||
| chr12:15521594
|
T | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1891+1282T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521594 | ||||||
| chr12:15521597
|
C | T | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.1891+1285C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15521597 | ||||||
| chr12:15522010
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1891+1698A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522010 | ||||||
| chr12:15522098
|
AATAATAA others(7): Show |
A | 3 | a0001c0002t0002g0076a0001c0002t0002g0135a0001c0002t0015g0095 | 3 | HG02809.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1891+1801_1891+181 others(18): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 15522098 | |||||
| chr12:15522110
|
T | A | 1 | a0001c0003t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1891+1798T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522110 | ||||||
| chr12:15522189
|
T | A | 78 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(75): Show | 78 | HG00423.hp2 HG00597.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1891+1877T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522189 | ||||||
| chr12:15522212
|
A | C | 74 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(71): Show | 74 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.1891+1900A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522212 | ||||||
| chr12:15522213
|
T | A | 74 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(71): Show | 74 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.1891+1901T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522213 | ||||||
| chr12:15522236
|
A | T | 74 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(71): Show | 74 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.1891+1924A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522236 | ||||||
| chr12:15522247
|
CT | C | 59 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0019others(56): Show | 59 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.1891+1949delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 15522247 | |||||
| chr12:15522536
|
G | A | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.1891+2224G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522536 | ||||||
| chr12:15522648
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0125a0001c0003t0001g0124others(2): Show | 5 | HG00621.hp2 HG02074.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1892-2166A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522648 | ||||||
| chr12:15522738
|
A | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-2076A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15522738 | ||||||
| chr12:15523004
|
G | T | 1 | a0001c0004t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1892-1810G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523004 | ||||||
| chr12:15523069
|
G | T | 1 | a0001c0007t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1892-1745G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523069 | ||||||
| chr12:15523127
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-1687A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523127 | ||||||
| chr12:15523191
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1892-1623G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523191 | ||||||
| chr12:15523205
|
T | C | 1 | a0001c0002t0006g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1892-1609T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523205 | ||||||
| chr12:15523227
|
C | T | 69 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(66): Show | 69 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(66): Show |
intron_variant | MODIFIER | c.1892-1587C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523227 | ||||||
| chr12:15523238
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1892-1576A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523238 | ||||||
| chr12:15523628
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1892-1186A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523628 | ||||||
| chr12:15523662
|
C | T | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1892-1152C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523662 | ||||||
| chr12:15523719
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.1892-1095A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523719 | ||||||
| chr12:15523889
|
C | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1892-925C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15523889 | ||||||
| chr12:15524108
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-706C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524108 | ||||||
| chr12:15524113
|
G | A | 2 | a0001c0002t0004g0163a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1892-701G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524113 | ||||||
| chr12:15524123
|
T | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1892-691T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524123 | ||||||
| chr12:15524157
|
T | TA | 34 | a0001c0001t0001g0020a0001c0001t0001g0088a0001c0001t0001g0110others(31): Show | 34 | HG01123.hp2 HG01169.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.1892-637dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 15524157 | |||||
| chr12:15524157
|
T | TAA | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(34): Show | 37 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1892-638_1892-637d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 15524157 | |||||
| chr12:15524157
|
T | TAAA | 27 | a0001c0001t0001g0002a0001c0001t0005g0103a0001c0002t0001g0008others(24): Show | 27 | HG00735.hp1 HG01109.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1892-639_1892-637d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 15524157 | |||||
| chr12:15524157
|
T | TAAAA | 7 | a0001c0002t0001g0137a0001c0002t0007g0080a0001c0005t0002g0109others(4): Show | 7 | HG00733.hp2 HG01981.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1892-640_1892-637d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr12 | 15524157 | |||||
| chr12:15524319
|
C | G | 1 | a0001c0002t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1892-495C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524319 | ||||||
| chr12:15524418
|
G | A | 68 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(65): Show | 68 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(65): Show |
intron_variant | MODIFIER | c.1892-396G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524418 | ||||||
| chr12:15524449
|
C | A | 5 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061others(2): Show | 5 | HG02258.hp1 HG03471.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1892-365C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524449 | ||||||
| chr12:15524452
|
A | T | 4 | a0001c0002t0003g0028a0001c0002t0004g0056a0001c0002t0008g0027others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1892-362A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524452 | ||||||
| chr12:15524470
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-344A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524470 | ||||||
| chr12:15524637
|
G | GTATCA | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-177_1892-176i others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524637 | ||||||
| chr12:15524639
|
C | CACTTGTT others(1): Show |
2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-175_1892-174i others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524639 | ||||||
| chr12:15524640
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-174C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524640 | ||||||
| chr12:15524756
|
G | A | 3 | a0001c0002t0004g0034a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-58G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524756 | ||||||
| chr12:15524775
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1892-39A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 10/26 | chr12 | 15524775 | ||||||
| chr12:15525058
|
A | T | 68 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(65): Show | 68 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(65): Show |
intron_variant | MODIFIER | c.2043+93A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525058 | ||||||
| chr12:15525116
|
G | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2043+151G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525116 | ||||||
| chr12:15525204
|
A | G | 74 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(71): Show | 74 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.2043+239A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525204 | ||||||
| chr12:15525214
|
C | A | 1 | a0001c0003t0001g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2043+249C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525214 | ||||||
| chr12:15525270
|
T | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2043+305T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525270 | ||||||
| chr12:15525337
|
A | AAATACGC others(24): Show |
1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2043+374_2043+404d others(33): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr12 | 15525337 | |||||
| chr12:15525413
|
G | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2043+448G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525413 | ||||||
| chr12:15525582
|
T | C | 73 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(70): Show | 73 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(70): Show |
intron_variant | MODIFIER | c.2044-560T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525582 | ||||||
| chr12:15525628
|
A | G | 72 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(69): Show | 72 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(69): Show |
intron_variant | MODIFIER | c.2044-514A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525628 | ||||||
| chr12:15525651
|
A | G | 1 | a0001c0002t0001g0132 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2044-491A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525651 | ||||||
| chr12:15525656
|
C | A | 5 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061others(2): Show | 5 | HG02258.hp1 HG03471.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-486C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525656 | ||||||
| chr12:15525707
|
A | G | 24 | a0001c0002t0001g0018a0001c0002t0003g0028a0001c0002t0004g0056others(21): Show | 24 | HG01123.hp2 HG01169.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2044-435A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525707 | ||||||
| chr12:15525776
|
C | T | 1 | a0001c0006t0004g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2044-366C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 11/26 | chr12 | 15525776 | ||||||
| chr12:15526274
|
G | A | 74 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(71): Show | 74 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.2164+12G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15526274 | ||||||
| chr12:15526614
|
C | T | 6 | a0001c0002t0007g0080a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164+352C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15526614 | ||||||
| chr12:15526619
|
ATATCT | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+360_2164+364d others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15526619 | |||||
| chr12:15526651
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+389C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15526651 | ||||||
| chr12:15526742
|
T | C | 77 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(74): Show | 77 | HG00423.hp2 HG00597.hp1 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.2164+480T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15526742 | ||||||
| chr12:15526779
|
C | A | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+517C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15526779 | ||||||
| chr12:15526914
|
TAAC | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+655_2164+657d others(5): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15526914 | |||||
| chr12:15527043
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2164+781G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15527043 | ||||||
| chr12:15527134
|
A | C | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+872A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15527134 | ||||||
| chr12:15527180
|
T | A | 4 | a0001c0001t0001g0119a0001c0001t0002g0069a0001c0001t0002g0146others(1): Show | 4 | HG01123.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+918T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15527180 | ||||||
| chr12:15527292
|
G | A | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+1030G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15527292 | ||||||
| chr12:15527555
|
CAGCACCA others(6): Show |
C | 4 | a0001c0003t0001g0074a0001c0003t0007g0081a0001c0003t0007g0164others(1): Show | 4 | HG00733.hp1 HG02258.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+1296_2164+130 others(17): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15527555 | |||||
| chr12:15527875
|
A | ACCCGCCC others(8): Show |
59 | a0001c0002t0001g0008a0001c0002t0001g0018a0001c0002t0001g0019others(56): Show | 59 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.2164+1622_2164+162 others(19): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15527875 | |||||
| chr12:15527875
|
A | ACCCGCCC others(9): Show |
17 | a0001c0002t0001g0013a0001c0002t0001g0137a0001c0002t0001g0139others(14): Show | 17 | HG00423.hp2 HG00597.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2164+1622_2164+162 others(20): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15527875 | |||||
| chr12:15527879
|
G | GCCCACCA others(8): Show |
1 | a0001c0002t0002g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2164+1622_2164+162 others(19): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15527879 | |||||
| chr12:15527943
|
C | T | 73 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(70): Show | 73 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(70): Show |
intron_variant | MODIFIER | c.2164+1681C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15527943 | ||||||
| chr12:15528164
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2164+1902C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528164 | ||||||
| chr12:15528165
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0006g0068 | 2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2164+1903A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528165 | ||||||
| chr12:15528236
|
G | C | 58 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(55): Show | 58 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.2164+1974G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528236 | ||||||
| chr12:15528360
|
CA | C | 53 | a0001c0001t0001g0130a0001c0002t0001g0008a0001c0002t0001g0013others(50): Show | 53 | HG00733.hp2 HG01167.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.2164+2114delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15528360 | |||||
| chr12:15528360
|
CAA | C | 9 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0064others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2164+2113_2164+211 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15528360 | |||||
| chr12:15528450
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.2164+2188A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528450 | ||||||
| chr12:15528457
|
G | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 8 | HG00621.hp2 HG02074.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.2164+2195G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528457 | ||||||
| chr12:15528461
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+2199C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528461 | ||||||
| chr12:15528522
|
C | CAA | 58 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(55): Show | 58 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.2164+2271_2164+227 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15528522 | |||||
| chr12:15528534
|
A | AAG | 5 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0065others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2164+2272_2164+227 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528534 | ||||||
| chr12:15528636
|
C | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+2374C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528636 | ||||||
| chr12:15528984
|
C | A | 64 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(61): Show | 64 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.2164+2722C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15528984 | ||||||
| chr12:15529425
|
G | C | 1 | a0001c0002t0003g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2164+3163G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15529425 | ||||||
| chr12:15529467
|
T | TA | 65 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(62): Show | 65 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.2164+3220dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15529467 | |||||
| chr12:15529467
|
TA | T | 5 | a0001c0001t0010g0022a0001c0001t0010g0023a0001c0002t0003g0133others(2): Show | 5 | HG02258.hp1 HG03471.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2164+3220delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15529467 | |||||
| chr12:15529773
|
A | G | 65 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(62): Show | 65 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.2164+3511A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15529773 | ||||||
| chr12:15529848
|
C | T | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+3586C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15529848 | ||||||
| chr12:15529853
|
G | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+3591G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15529853 | ||||||
| chr12:15529951
|
C | T | 3 | a0001c0002t0003g0066a0001c0002t0003g0079a0001c0002t0003g0116 | 3 | HG02451.hp2 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2164+3689C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15529951 | ||||||
| chr12:15529970
|
G | A | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.2164+3708G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15529970 | ||||||
| chr12:15530006
|
T | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+3744T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530006 | ||||||
| chr12:15530097
|
G | A | 1 | a0001c0002t0003g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2164+3835G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530097 | ||||||
| chr12:15530176
|
A | G | 1 | a0001c0002t0002g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2164+3914A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530176 | ||||||
| chr12:15530217
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+3955T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530217 | ||||||
| chr12:15530276
|
T | C | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+4014T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530276 | ||||||
| chr12:15530425
|
C | G | 1 | a0001c0003t0001g0150 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2164+4163C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530425 | ||||||
| chr12:15530510
|
A | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2164+4248A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530510 | ||||||
| chr12:15530536
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2164+4274C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530536 | ||||||
| chr12:15530618
|
T | C | 1 | a0001c0002t0002g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2164+4356T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530618 | ||||||
| chr12:15530626
|
C | G | 2 | a0001c0002t0003g0028a0001c0002t0008g0027 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2164+4364C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530626 | ||||||
| chr12:15530968
|
C | T | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2164+4706C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530968 | ||||||
| chr12:15530982
|
G | C | 2 | a0001c0002t0004g0163a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2164+4720G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15530982 | ||||||
| chr12:15531101
|
A | G | 2 | a0001c0002t0001g0137a0001c0002t0003g0129 | 2 | HG01167.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2164+4839A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531101 | ||||||
| chr12:15531138
|
A | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+4876A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531138 | ||||||
| chr12:15531184
|
C | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+4922C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531184 | ||||||
| chr12:15531197
|
G | T | 1 | a0001c0002t0003g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2164+4935G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531197 | ||||||
| chr12:15531508
|
T | C | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+5246T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531508 | ||||||
| chr12:15531575
|
G | A | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2164+5313G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531575 | ||||||
| chr12:15531932
|
A | G | 1 | a0001c0002t0012g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2164+5670A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531932 | ||||||
| chr12:15531994
|
T | C | 35 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0019others(32): Show | 35 | HG00733.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.2164+5732T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531994 | ||||||
| chr12:15531999
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2164+5737G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15531999 | ||||||
| chr12:15532033
|
C | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+5771C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15532033 | ||||||
| chr12:15532041
|
C | T | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+5779C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15532041 | ||||||
| chr12:15532100
|
A | T | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2164+5838A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15532100 | ||||||
| chr12:15532142
|
A | T | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.2164+5880A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15532142 | ||||||
| chr12:15532213
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2164+5951G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15532213 | ||||||
| chr12:15532300
|
A | G | 65 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(62): Show | 65 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.2164+6038A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15532300 | ||||||
| chr12:15532362
|
G | A | 1 | a0001c0002t0002g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2164+6100G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15532362 | ||||||
| chr12:15533048
|
C | T | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+6786C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533048 | ||||||
| chr12:15533056
|
A | G | 65 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(62): Show | 65 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.2164+6794A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533056 | ||||||
| chr12:15533578
|
C | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2164+7316C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533578 | ||||||
| chr12:15533687
|
A | C | 1 | a0001c0002t0002g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2164+7425A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533687 | ||||||
| chr12:15533750
|
T | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2164+7488T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533750 | ||||||
| chr12:15533825
|
C | T | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2164+7563C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533825 | ||||||
| chr12:15533851
|
T | C | 63 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(60): Show | 63 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.2164+7589T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533851 | ||||||
| chr12:15533863
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2164+7601T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533863 | ||||||
| chr12:15533906
|
A | G | 71 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(68): Show | 71 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.2164+7644A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15533906 | ||||||
| chr12:15534102
|
C | A | 1 | a0001c0001t0006g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2164+7840C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534102 | ||||||
| chr12:15534162
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.2164+7900G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534162 | ||||||
| chr12:15534309
|
A | G | 2 | a0001c0002t0004g0056a0001c0002t0011g0082 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2164+8047A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534309 | ||||||
| chr12:15534387
|
A | G | 3 | a0001c0002t0003g0028a0001c0002t0004g0034a0001c0002t0008g0027 | 3 | HG02630.hp1 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2164+8125A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534387 | ||||||
| chr12:15534434
|
A | G | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+8172A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534434 | ||||||
| chr12:15534447
|
G | A | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+8185G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534447 | ||||||
| chr12:15534469
|
G | A | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2164+8207G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534469 | ||||||
| chr12:15534505
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2164+8243C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534505 | ||||||
| chr12:15534573
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2164+8311C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534573 | ||||||
| chr12:15534679
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2164+8417C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534679 | ||||||
| chr12:15534825
|
T | A | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+8563T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534825 | ||||||
| chr12:15534935
|
G | A | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2164+8673G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15534935 | ||||||
| chr12:15535113
|
A | T | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2164+8851A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15535113 | ||||||
| chr12:15535240
|
T | C | 43 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0019others(40): Show | 43 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.2164+8978T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15535240 | ||||||
| chr12:15535256
|
T | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.2164+8994T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15535256 | ||||||
| chr12:15535421
|
G | GAAAAC | 4 | a0001c0002t0003g0028a0001c0002t0004g0034a0001c0002t0006g0058others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+9179_2164+918 others(9): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15535421 | |||||
| chr12:15535596
|
G | A | 9 | a0001c0002t0001g0032a0001c0002t0001g0077a0001c0002t0002g0031others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2164+9334G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15535596 | ||||||
| chr12:15535614
|
C | T | 2 | a0001c0002t0004g0163a0001c0002t0012g0084 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2164+9352C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15535614 | ||||||
| chr12:15535697
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2164+9435G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15535697 | ||||||
| chr12:15535765
|
T | C | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2164+9503T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15535765 | ||||||
| chr12:15535950
|
TTC | T | 4 | a0001c0002t0003g0028a0001c0002t0008g0027a0001c0008t0004g0040others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+9694_2164+969 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15535950 | |||||
| chr12:15536053
|
T | TTAA | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 46 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2164+9791_2164+979 others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536053 | ||||||
| chr12:15536053
|
TA | T | 9 | a0001c0002t0001g0032a0001c0002t0001g0077a0001c0002t0002g0031others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2164+9797delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15536053 | |||||
| chr12:15536054
|
A | T | 101 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0042others(98): Show | 101 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.2164+9792A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536054 | ||||||
| chr12:15536167
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2164+9905C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536167 | ||||||
| chr12:15536270
|
G | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(39): Show | 42 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2164+10008G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536270 | ||||||
| chr12:15536406
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0088a0001c0001t0001g0090others(1): Show | 4 | NA18942.hp1 NA18949.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+10144G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536406 | ||||||
| chr12:15536484
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.2165-10085A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536484 | ||||||
| chr12:15536615
|
G | A | 1 | a0001c0001t0006g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2165-9954G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536615 | ||||||
| chr12:15536629
|
G | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0120others(15): Show | 18 | HG00597.hp1 HG01074.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2165-9940G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536629 | ||||||
| chr12:15536929
|
G | C | 1 | a0001c0002t0003g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2165-9640G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15536929 | ||||||
| chr12:15537002
|
G | A | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-9567G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537002 | ||||||
| chr12:15537017
|
G | A | 69 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(66): Show | 69 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.2165-9552G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537017 | ||||||
| chr12:15537074
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2165-9495G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537074 | ||||||
| chr12:15537152
|
C | T | 3 | a0001c0002t0004g0034a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-9417C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537152 | ||||||
| chr12:15537193
|
G | A | 3 | a0001c0002t0006g0058a0001c0002t0006g0059a0001c0002t0006g0162 | 3 | HG02109.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2165-9376G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537193 | ||||||
| chr12:15537238
|
G | T | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2165-9331G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537238 | ||||||
| chr12:15537270
|
C | T | 34 | a0001c0001t0003g0030a0001c0002t0001g0008a0001c0002t0001g0013others(31): Show | 34 | HG00733.hp2 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2165-9299C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537270 | ||||||
| chr12:15537391
|
C | T | 3 | a0001c0001t0006g0068a0001c0002t0004g0056a0001c0002t0011g0082 | 3 | HG01261.hp2 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2165-9178C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537391 | ||||||
| chr12:15537519
|
G | A | 1 | a0001c0007t0001g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2165-9050G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537519 | ||||||
| chr12:15537633
|
A | G | 3 | a0001c0004t0001g0099a0001c0004t0001g0100a0001c0004t0001g0147 | 3 | HG01243.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2165-8936A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537633 | ||||||
| chr12:15537690
|
T | C | 1 | a0001c0002t0003g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2165-8879T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537690 | ||||||
| chr12:15537799
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.2165-8770C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537799 | ||||||
| chr12:15537907
|
G | A | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-8662G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15537907 | ||||||
| chr12:15538167
|
C | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-8402C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15538167 | ||||||
| chr12:15538239
|
C | CT | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(106): Show | 109 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.2165-8319dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15538239 | |||||
| chr12:15538245
|
T | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-8324T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15538245 | ||||||
| chr12:15538408
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-8161A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15538408 | ||||||
| chr12:15538706
|
C | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(34): Show | 37 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2165-7863C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15538706 | ||||||
| chr12:15538765
|
T | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(56): Show | 59 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.2165-7804T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15538765 | ||||||
| chr12:15538771
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(56): Show | 59 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.2165-7798G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15538771 | ||||||
| chr12:15538965
|
A | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(56): Show | 59 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.2165-7604A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15538965 | ||||||
| chr12:15539325
|
A | T | 15 | a0001c0002t0001g0035a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2165-7244A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539325 | ||||||
| chr12:15539358
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(34): Show | 37 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2165-7211C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539358 | ||||||
| chr12:15539514
|
C | A | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-7055C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539514 | ||||||
| chr12:15539572
|
C | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-6997C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539572 | ||||||
| chr12:15539581
|
G | T | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2165-6988G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539581 | ||||||
| chr12:15539651
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(56): Show | 59 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.2165-6918G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539651 | ||||||
| chr12:15539669
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2165-6900G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539669 | ||||||
| chr12:15539706
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2165-6863G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539706 | ||||||
| chr12:15539722
|
G | A | 9 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0004g0163others(6): Show | 9 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2165-6847G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539722 | ||||||
| chr12:15539748
|
T | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2165-6821T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539748 | ||||||
| chr12:15539761
|
C | CA | 5 | a0001c0002t0002g0031a0001c0002t0003g0033a0001c0002t0003g0041others(2): Show | 5 | HG01169.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-6774dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15539761 | |||||
| chr12:15539761
|
CAA | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0113others(2): Show | 5 | HG00673.hp1 HG02300.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-6775_2165-677 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15539761 | |||||
| chr12:15539761
|
CAAA | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0042others(14): Show | 17 | HG00597.hp2 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2165-6776_2165-677 others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15539761 | |||||
| chr12:15539761
|
CAAAA | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(61): Show | 64 | HG00423.hp1 HG00621.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.2165-6777_2165-677 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15539761 | |||||
| chr12:15539761
|
CAAAAA | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(36): Show | 39 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.2165-6778_2165-677 others(9): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15539761 | |||||
| chr12:15539761
|
CAAAAAA | C | 13 | a0001c0002t0001g0035a0001c0002t0002g0050a0001c0002t0002g0063others(10): Show | 13 | HG01109.hp1 HG02723.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.2165-6779_2165-677 others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15539761 | |||||
| chr12:15539761
|
CAAAAAAA | C | 7 | a0001c0001t0001g0144a0001c0001t0003g0030a0001c0002t0003g0028others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2165-6780_2165-677 others(11): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15539761 | |||||
| chr12:15539797
|
A | G | 1 | a0001c0001t0006g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2165-6772A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539797 | ||||||
| chr12:15539939
|
T | G | 1 | a0001c0002t0003g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2165-6630T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539939 | ||||||
| chr12:15539961
|
T | A | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-6608T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15539961 | ||||||
| chr12:15540033
|
A | G | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-6536A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15540033 | ||||||
| chr12:15540242
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2165-6327T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15540242 | ||||||
| chr12:15540375
|
T | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-6194T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15540375 | ||||||
| chr12:15540468
|
C | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-6101C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15540468 | ||||||
| chr12:15540611
|
G | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-5958G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15540611 | ||||||
| chr12:15540769
|
C | A | 1 | a0001c0004t0002g0127 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2165-5800C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15540769 | ||||||
| chr12:15540961
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0101others(3): Show | 6 | HG00673.hp1 HG02083.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.2165-5608A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15540961 | ||||||
| chr12:15541058
|
T | G | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2165-5511T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15541058 | ||||||
| chr12:15541676
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-4893A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15541676 | ||||||
| chr12:15541681
|
G | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149 | 3 | HG02145.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2165-4888G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15541681 | ||||||
| chr12:15541810
|
G | A | 2 | a0001c0002t0003g0028a0001c0002t0008g0027 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2165-4759G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15541810 | ||||||
| chr12:15541810
|
G | C | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-4759G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15541810 | ||||||
| chr12:15541986
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2165-4583G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15541986 | ||||||
| chr12:15542022
|
T | A | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2165-4547T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542022 | ||||||
| chr12:15542046
|
G | T | 1 | a0001c0003t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2165-4523G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542046 | ||||||
| chr12:15542073
|
C | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-4496C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542073 | ||||||
| chr12:15542202
|
C | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0020others(91): Show | 94 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.2165-4367C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542202 | ||||||
| chr12:15542270
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2165-4299C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542270 | ||||||
| chr12:15542347
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 154 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.2165-4222G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542347 | ||||||
| chr12:15542482
|
G | A | 1 | a0001c0003t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2165-4087G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542482 | ||||||
| chr12:15542694
|
G | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0020others(88): Show | 91 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.2165-3875G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542694 | ||||||
| chr12:15542699
|
C | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2165-3870C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542699 | ||||||
| chr12:15542901
|
G | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0020others(88): Show | 91 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.2165-3668G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15542901 | ||||||
| chr12:15543542
|
C | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-3027C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15543542 | ||||||
| chr12:15543587
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2165-2982G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15543587 | ||||||
| chr12:15543796
|
C | A | 2 | a0001c0004t0001g0099a0001c0004t0001g0100 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2165-2773C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15543796 | ||||||
| chr12:15544001
|
A | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-2568A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544001 | ||||||
| chr12:15544141
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2165-2428G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544141 | ||||||
| chr12:15544250
|
C | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-2319C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544250 | ||||||
| chr12:15544384
|
A | G | 13 | a0001c0002t0001g0035a0001c0002t0002g0050a0001c0002t0002g0062others(10): Show | 13 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2165-2185A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544384 | ||||||
| chr12:15544412
|
G | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-2157G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544412 | ||||||
| chr12:15544493
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(32): Show | 35 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2165-2076C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544493 | ||||||
| chr12:15544503
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(32): Show | 35 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2165-2066T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544503 | ||||||
| chr12:15544506
|
C | A | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2165-2063C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544506 | ||||||
| chr12:15544506
|
C | CAA | 21 | a0001c0001t0003g0030a0001c0001t0004g0115a0001c0002t0001g0035others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.2165-2043_2165-204 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15544506 | |||||
| chr12:15544506
|
C | CAAAA | 27 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(24): Show | 27 | HG00673.hp2 HG01074.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.2165-2045_2165-204 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15544506 | |||||
| chr12:15544506
|
C | CAAAAA | 5 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0073others(2): Show | 5 | HG00735.hp1 HG02738.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-2046_2165-204 others(9): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15544506 | |||||
| chr12:15544532
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-2037A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544532 | ||||||
| chr12:15544743
|
A | G | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2165-1826A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544743 | ||||||
| chr12:15544752
|
A | T | 1 | a0001c0003t0001g0038 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2165-1817A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544752 | ||||||
| chr12:15544826
|
C | T | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-1743C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544826 | ||||||
| chr12:15544933
|
T | A | 13 | a0001c0002t0001g0035a0001c0002t0002g0050a0001c0002t0002g0062others(10): Show | 13 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2165-1636T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15544933 | ||||||
| chr12:15545008
|
T | C | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2165-1561T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545008 | ||||||
| chr12:15545358
|
G | A | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2165-1211G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545358 | ||||||
| chr12:15545370
|
G | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-1199G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545370 | ||||||
| chr12:15545615
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2165-954G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545615 | ||||||
| chr12:15545632
|
C | T | 1 | a0001c0003t0001g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2165-937C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545632 | ||||||
| chr12:15545709
|
C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2165-860C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545709 | ||||||
| chr12:15545820
|
G | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2165-749G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545820 | ||||||
| chr12:15545850
|
A | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(32): Show | 35 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2165-719A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545850 | ||||||
| chr12:15545858
|
A | C | 3 | a0001c0004t0001g0099a0001c0004t0001g0100a0001c0004t0001g0147 | 3 | HG01243.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2165-711A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545858 | ||||||
| chr12:15545878
|
G | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(47): Show | 50 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2165-691G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545878 | ||||||
| chr12:15545970
|
G | A | 1 | a0001c0001t0008g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2165-599G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545970 | ||||||
| chr12:15545987
|
C | T | 3 | a0001c0001t0004g0115a0001c0002t0004g0034a0001c0002t0008g0052 | 3 | HG02257.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2165-582C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15545987 | ||||||
| chr12:15546015
|
CAA | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(51): Show | 54 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2165-540_2165-539d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr12 | 15546015 | |||||
| chr12:15546179
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0093 | 2 | HG00735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2165-390G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15546179 | ||||||
| chr12:15546303
|
T | G | 5 | a0001c0005t0002g0109a0001c0005t0005g0096a0001c0005t0005g0097others(2): Show | 5 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2165-266T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15546303 | ||||||
| chr12:15546539
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165-30A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15546539 | ||||||
| chr12:15546564
|
C | A | 1 | a0001c0002t0001g0019 | 1 | HG04184.hp1 | splice_region_variant&intron_variant | LOW | c.2165-5C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 12/26 | chr12 | 15546564 | ||||||
| chr12:15546754
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2304+46G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15546754 | ||||||
| chr12:15546838
|
C | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(57): Show | 60 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.2304+130C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15546838 | ||||||
| chr12:15547345
|
T | C | 3 | a0001c0001t0004g0115a0001c0002t0004g0034a0001c0002t0008g0052 | 3 | HG02257.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2304+637T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15547345 | ||||||
| chr12:15547366
|
G | A | 10 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2304+658G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15547366 | ||||||
| chr12:15547923
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(49): Show | 52 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2305-1171A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15547923 | ||||||
| chr12:15548013
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2305-1081C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15548013 | ||||||
| chr12:15548014
|
G | A | 3 | a0001c0001t0004g0115a0001c0002t0004g0034a0001c0002t0008g0052 | 3 | HG02257.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2305-1080G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15548014 | ||||||
| chr12:15548116
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2305-978A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15548116 | ||||||
| chr12:15548202
|
TA | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(49): Show | 52 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2305-882delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548202 | |||||
| chr12:15548470
|
G | T | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2305-624G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15548470 | ||||||
| chr12:15548520
|
GTA | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2305-566_2305-565d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548520 | |||||
| chr12:15548528
|
A | ATG | 17 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0130others(14): Show | 17 | HG01074.hp2 HG01109.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2305-542_2305-541d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548528 | |||||
| chr12:15548528
|
A | ATGTG | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.2305-544_2305-541d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548528 | |||||
| chr12:15548528
|
A | ATGTGTG | 5 | a0001c0001t0001g0122a0001c0001t0003g0030a0001c0001t0006g0094others(2): Show | 5 | HG02083.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2305-546_2305-541d others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548528 | |||||
| chr12:15548528
|
ATG | A | 2 | a0001c0008t0004g0040a0001c0008t0004g0071 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2305-542_2305-541d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548528 | |||||
| chr12:15548528
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2305-550_2305-541d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548528 | |||||
| chr12:15548528
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2305-552_2305-541d others(14): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr12 | 15548528 | |||||
| chr12:15548825
|
T | C | 2 | a0001c0001t0001g0078a0001c0002t0007g0080 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2305-269T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15548825 | ||||||
| chr12:15548918
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2305-176G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15548918 | ||||||
| chr12:15549073
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2305-21C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 13/26 | chr12 | 15549073 | ||||||
| chr12:15549245
|
G | GAAATCTG others(30): Show |
3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+19_2437+20ins others(37): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15549245 | ||||||
| chr12:15549246
|
T | C | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+20T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15549246 | ||||||
| chr12:15549250
|
A | T | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+24A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15549250 | ||||||
| chr12:15549268
|
A | AAT | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2437+57_2437+58dup others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr12 | 15549268 | |||||
| chr12:15549268
|
AAT | A | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+57_2437+58del others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr12 | 15549268 | |||||
| chr12:15549602
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(32): Show | 35 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2437+376C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15549602 | ||||||
| chr12:15549603
|
G | A | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+377G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15549603 | ||||||
| chr12:15549899
|
C | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2437+673C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15549899 | ||||||
| chr12:15550047
|
G | C | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+821G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550047 | ||||||
| chr12:15550079
|
T | C | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+853T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550079 | ||||||
| chr12:15550118
|
T | C | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2437+892T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550118 | ||||||
| chr12:15550186
|
C | T | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2437+960C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550186 | ||||||
| chr12:15550197
|
A | G | 5 | a0001c0002t0001g0018a0001c0004t0001g0005a0001c0004t0001g0007others(2): Show | 5 | HG01123.hp2 HG01169.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.2437+971A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550197 | ||||||
| chr12:15550199
|
G | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0093a0001c0001t0001g0148others(2): Show | 5 | HG00735.hp2 HG01074.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.2437+973G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550199 | ||||||
| chr12:15550245
|
A | G | 2 | a0001c0001t0001g0120a0002c0011t0001g0092 | 2 | HG01074.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2437+1019A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550245 | ||||||
| chr12:15550372
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2437+1146A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550372 | ||||||
| chr12:15550538
|
T | C | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2438-1013T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550538 | ||||||
| chr12:15550615
|
G | A | 1 | a0001c0002t0003g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2438-936G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550615 | ||||||
| chr12:15550638
|
C | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2438-913C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550638 | ||||||
| chr12:15550851
|
T | C | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2438-700T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550851 | ||||||
| chr12:15550915
|
G | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2438-636G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550915 | ||||||
| chr12:15550932
|
G | A | 2 | a0001c0001t0001g0078a0001c0002t0007g0080 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2438-619G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550932 | ||||||
| chr12:15550949
|
G | A | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2438-602G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15550949 | ||||||
| chr12:15551004
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(48): Show | 51 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.2438-547C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15551004 | ||||||
| chr12:15551207
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2438-344T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15551207 | ||||||
| chr12:15551216
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.2438-335G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15551216 | ||||||
| chr12:15551352
|
C | G | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2438-199C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15551352 | ||||||
| chr12:15551442
|
G | A | 1 | a0001c0002t0001g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2438-109G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15551442 | ||||||
| chr12:15551491
|
G | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2438-60G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 14/26 | chr12 | 15551491 | ||||||
| chr12:15551999
|
A | T | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2558+328A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15551999 | ||||||
| chr12:15552079
|
C | T | 1 | a0001c0004t0001g0017 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2558+408C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15552079 | ||||||
| chr12:15552427
|
C | T | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2558+756C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15552427 | ||||||
| chr12:15552564
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0009g0015a0001c0001t0009g0046others(1): Show | 4 | HG00621.hp1 HG00673.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.2558+893C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15552564 | ||||||
| chr12:15552659
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2558+988T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15552659 | ||||||
| chr12:15552795
|
C | CT | 66 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0037others(63): Show | 66 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.2558+1146dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15552795 | |||||
| chr12:15552795
|
C | CTT | 25 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2558+1145_2558+114 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15552795 | |||||
| chr12:15552795
|
C | CTTT | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(39): Show | 42 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2558+1144_2558+114 others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15552795 | |||||
| chr12:15552986
|
C | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(57): Show | 60 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.2558+1315C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15552986 | ||||||
| chr12:15553014
|
T | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2558+1343T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15553014 | ||||||
| chr12:15553082
|
G | C | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2558+1411G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15553082 | ||||||
| chr12:15553179
|
A | G | 5 | a0001c0001t0004g0115a0001c0002t0004g0034a0001c0002t0008g0052others(2): Show | 5 | HG02257.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2558+1508A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15553179 | ||||||
| chr12:15553189
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2558+1518A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15553189 | ||||||
| chr12:15553507
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2558+1836A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15553507 | ||||||
| chr12:15553985
|
G | A | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2558+2314G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15553985 | ||||||
| chr12:15553992
|
C | T | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2558+2321C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15553992 | ||||||
| chr12:15554054
|
C | T | 1 | a0001c0003t0001g0036 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2558+2383C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554054 | ||||||
| chr12:15554117
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(55): Show | 58 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.2558+2446A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554117 | ||||||
| chr12:15554132
|
G | A | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2558+2461G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554132 | ||||||
| chr12:15554198
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(40): Show | 43 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.2558+2527G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554198 | ||||||
| chr12:15554243
|
G | A | 2 | a0001c0001t0007g0083a0001c0001t0007g0085 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2558+2572G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554243 | ||||||
| chr12:15554313
|
GA | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2558+2645delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15554313 | |||||
| chr12:15554414
|
G | GTA | 13 | a0001c0001t0001g0122a0001c0002t0002g0050a0001c0002t0002g0062others(10): Show | 13 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2558+2757_2558+275 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15554414 | |||||
| chr12:15554414
|
GTA | G | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0012g0084others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2558+2757_2558+275 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15554414 | |||||
| chr12:15554456
|
T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(34): Show | 37 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2558+2785T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554456 | ||||||
| chr12:15554526
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2558+2855T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554526 | ||||||
| chr12:15554746
|
T | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(59): Show | 62 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.2559-2709T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15554746 | ||||||
| chr12:15555081
|
CA | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 155 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.2559-2367delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15555081 | |||||
| chr12:15555174
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2559-2281G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555174 | ||||||
| chr12:15555202
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2559-2253C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555202 | ||||||
| chr12:15555219
|
C | T | 1 | a0001c0003t0007g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2559-2236C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555219 | ||||||
| chr12:15555291
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2559-2164A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555291 | ||||||
| chr12:15555316
|
A | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(40): Show | 43 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.2559-2139A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555316 | ||||||
| chr12:15555736
|
T | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2559-1719T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555736 | ||||||
| chr12:15555914
|
G | A | 1 | a0001c0012t0006g0070 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2559-1541G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555914 | ||||||
| chr12:15555940
|
A | G | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2559-1515A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15555940 | ||||||
| chr12:15556149
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2559-1306A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556149 | ||||||
| chr12:15556211
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2559-1244A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556211 | ||||||
| chr12:15556240
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2559-1215T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556240 | ||||||
| chr12:15556372
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2559-1083T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556372 | ||||||
| chr12:15556376
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2559-1079G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556376 | ||||||
| chr12:15556399
|
T | A | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2559-1056T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556399 | ||||||
| chr12:15556611
|
C | A | 1 | a0001c0001t0005g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2559-844C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556611 | ||||||
| chr12:15556642
|
C | T | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2559-813C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556642 | ||||||
| chr12:15556664
|
A | G | 3 | a0001c0004t0001g0099a0001c0004t0001g0100a0001c0004t0001g0147 | 3 | HG01243.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2559-791A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556664 | ||||||
| chr12:15556705
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2559-750T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556705 | ||||||
| chr12:15556746
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0073 | 2 | NA18962.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2559-709A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556746 | ||||||
| chr12:15556779
|
T | A | 1 | a0001c0002t0001g0117 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2559-676T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556779 | ||||||
| chr12:15556856
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2559-599A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15556856 | ||||||
| chr12:15557032
|
G | GT | 18 | a0001c0001t0001g0144a0001c0002t0001g0008a0001c0002t0001g0013others(15): Show | 18 | HG01243.hp1 HG01981.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2559-409dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15557032 | |||||
| chr12:15557032
|
G | T | 1 | a0001c0002t0002g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2559-423G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15557032 | ||||||
| chr12:15557032
|
GTT | G | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2559-410_2559-409d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr12 | 15557032 | |||||
| chr12:15557336
|
C | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(34): Show | 37 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2559-119C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15557336 | ||||||
| chr12:15557427
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2559-28C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 15/26 | chr12 | 15557427 | ||||||
| chr12:15557555
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2627+32A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15557555 | ||||||
| chr12:15557605
|
G | A | 3 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0016g0061 | 3 | HG02258.hp1 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2627+82G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15557605 | ||||||
| chr12:15557971
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2627+448T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15557971 | ||||||
| chr12:15558023
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2627+500C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15558023 | ||||||
| chr12:15558079
|
C | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(43): Show | 46 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2627+556C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15558079 | ||||||
| chr12:15558498
|
A | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2627+975A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15558498 | ||||||
| chr12:15558826
|
G | A | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2627+1303G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15558826 | ||||||
| chr12:15558852
|
G | A | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2627+1329G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15558852 | ||||||
| chr12:15558999
|
C | G | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2628-1194C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15558999 | ||||||
| chr12:15559195
|
C | T | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2628-998C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15559195 | ||||||
| chr12:15559225
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2628-968A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15559225 | ||||||
| chr12:15559348
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2628-845C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15559348 | ||||||
| chr12:15559618
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2628-575A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15559618 | ||||||
| chr12:15559835
|
A | T | 6 | a0001c0002t0012g0084a0001c0005t0002g0109a0001c0005t0005g0096others(3): Show | 6 | HG00733.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2628-358A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15559835 | ||||||
| chr12:15560123
|
A | G | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2628-70A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15560123 | ||||||
| chr12:15560136
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2628-57A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 16/26 | chr12 | 15560136 | ||||||
| chr12:15560538
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2711+262T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15560538 | ||||||
| chr12:15560589
|
C | T | 12 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2711+313C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15560589 | ||||||
| chr12:15560775
|
G | A | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2711+499G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15560775 | ||||||
| chr12:15560835
|
A | G | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2711+559A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15560835 | ||||||
| chr12:15560962
|
G | A | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2711+686G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15560962 | ||||||
| chr12:15561018
|
G | A | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2711+742G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15561018 | ||||||
| chr12:15561103
|
G | A | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2711+827G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15561103 | ||||||
| chr12:15561275
|
A | G | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2711+999A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15561275 | ||||||
| chr12:15561764
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2711+1488A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15561764 | ||||||
| chr12:15561813
|
A | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0093a0001c0001t0001g0148others(1): Show | 4 | HG00735.hp2 HG01074.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2711+1537A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15561813 | ||||||
| chr12:15561830
|
T | C | 15 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2711+1554T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15561830 | ||||||
| chr12:15562105
|
G | A | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2711+1829G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15562105 | ||||||
| chr12:15562134
|
A | G | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(43): Show | 46 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2711+1858A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15562134 | ||||||
| chr12:15562417
|
G | GACGCACA others(5): Show |
1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2711+2142_2711+215 others(16): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr12 | 15562417 | |||||
| chr12:15562741
|
C | CT | 91 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0020others(88): Show | 91 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.2711+2480dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr12 | 15562741 | |||||
| chr12:15562790
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0007t0001g0053 | 3 | HG00423.hp1 NA19066.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2711+2514A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15562790 | ||||||
| chr12:15562911
|
A | C | 14 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(11): Show | 14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2711+2635A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15562911 | ||||||
| chr12:15563132
|
T | C | 1 | a0001c0002t0007g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2712-2461T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15563132 | ||||||
| chr12:15563291
|
C | T | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2712-2302C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15563291 | ||||||
| chr12:15563316
|
C | CACAT | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(34): Show | 37 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2712-2275_2712-227 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr12 | 15563316 | |||||
| chr12:15563788
|
T | C | 18 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(15): Show | 18 | HG00423.hp2 HG00597.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2712-1805T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15563788 | ||||||
| chr12:15563981
|
G | A | 1 | a0001c0003t0007g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2712-1612G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15563981 | ||||||
| chr12:15564256
|
C | T | 16 | a0001c0001t0004g0115a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 16 | HG01109.hp1 HG01109.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2712-1337C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564256 | ||||||
| chr12:15564258
|
T | A | 1 | a0001c0003t0007g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2712-1335T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564258 | ||||||
| chr12:15564379
|
A | G | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2712-1214A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564379 | ||||||
| chr12:15564385
|
T | C | 2 | a0001c0004t0001g0007a0003c0010t0013g0054 | 2 | HG01169.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2712-1208T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564385 | ||||||
| chr12:15564412
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2712-1181G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564412 | ||||||
| chr12:15564462
|
A | C | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2712-1131A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564462 | ||||||
| chr12:15564474
|
G | C | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2712-1119G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564474 | ||||||
| chr12:15564679
|
C | G | 3 | a0001c0001t0003g0030a0001c0002t0003g0028a0001c0002t0008g0027 | 3 | HG02559.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2712-914C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15564679 | ||||||
| chr12:15565186
|
A | G | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2712-407A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15565186 | ||||||
| chr12:15565218
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2712-375T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15565218 | ||||||
| chr12:15565436
|
T | C | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2712-157T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15565436 | ||||||
| chr12:15565450
|
G | GTAAT | 18 | a0001c0001t0004g0115a0001c0002t0002g0050a0001c0002t0002g0062others(15): Show | 18 | HG00423.hp2 HG00597.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2712-140_2712-139i others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr12 | 15565450 | |||||
| chr12:15565501
|
T | A | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2712-92T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 17/26 | chr12 | 15565501 | ||||||
| chr12:15565698
|
T | G | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2747+70T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15565698 | ||||||
| chr12:15565721
|
C | T | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2747+93C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15565721 | ||||||
| chr12:15565827
|
A | G | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2747+199A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15565827 | ||||||
| chr12:15566139
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2747+511A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15566139 | ||||||
| chr12:15566146
|
T | C | 4 | a0001c0002t0003g0133a0001c0002t0003g0143a0001c0002t0008g0052others(1): Show | 4 | HG02258.hp1 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2747+518T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15566146 | ||||||
| chr12:15566200
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2747+572A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15566200 | ||||||
| chr12:15566375
|
T | C | 1 | a0001c0002t0001g0013 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2747+747T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15566375 | ||||||
| chr12:15566646
|
C | G | 1 | a0001c0004t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2747+1018C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15566646 | ||||||
| chr12:15566766
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2747+1138C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15566766 | ||||||
| chr12:15567095
|
A | G | 9 | a0001c0001t0003g0030a0001c0001t0003g0060a0001c0002t0003g0028others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2747+1467A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567095 | ||||||
| chr12:15567110
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2747+1482A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567110 | ||||||
| chr12:15567223
|
C | T | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2747+1595C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567223 | ||||||
| chr12:15567230
|
A | G | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2747+1602A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567230 | ||||||
| chr12:15567282
|
T | C | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2747+1654T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567282 | ||||||
| chr12:15567315
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(62): Show | 65 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.2747+1687A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567315 | ||||||
| chr12:15567398
|
CT | C | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2747+1771delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567398 | ||||||
| chr12:15567510
|
C | G | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2747+1882C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567510 | ||||||
| chr12:15567644
|
T | A | 1 | a0001c0001t0001g0091 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2748-1773T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567644 | ||||||
| chr12:15567842
|
C | T | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748-1575C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567842 | ||||||
| chr12:15567997
|
C | A | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748-1420C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15567997 | ||||||
| chr12:15568100
|
C | G | 1 | a0001c0004t0001g0017 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2748-1317C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568100 | ||||||
| chr12:15568153
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2748-1264G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568153 | ||||||
| chr12:15568167
|
C | T | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748-1250C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568167 | ||||||
| chr12:15568199
|
G | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2748-1218G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568199 | ||||||
| chr12:15568428
|
T | TCAAAA | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(39): Show | 42 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2748-958_2748-954d others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr12 | 15568428 | |||||
| chr12:15568428
|
T | TCAAAACA others(3): Show |
1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2748-963_2748-954d others(12): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr12 | 15568428 | |||||
| chr12:15568428
|
TCAAAA | T | 7 | a0001c0001t0004g0115a0001c0006t0004g0045a0001c0006t0004g0114others(4): Show | 7 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2748-958_2748-954d others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr12 | 15568428 | |||||
| chr12:15568428
|
TCAAAACA others(8): Show |
T | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748-968_2748-954d others(17): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr12 | 15568428 | |||||
| chr12:15568440
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2748-977A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568440 | ||||||
| chr12:15568560
|
A | G | 5 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0065others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2748-857A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568560 | ||||||
| chr12:15568578
|
T | A | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2748-839T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568578 | ||||||
| chr12:15568686
|
C | CA | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748-723dupA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr12 | 15568686 | |||||
| chr12:15568704
|
T | G | 3 | a0001c0002t0004g0056a0001c0002t0011g0082a0001c0002t0015g0095 | 3 | HG02109.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2748-713T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15568704 | ||||||
| chr12:15569144
|
T | C | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2748-273T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15569144 | ||||||
| chr12:15569152
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2748-265T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15569152 | ||||||
| chr12:15569312
|
C | T | 3 | a0001c0001t0004g0115a0001c0008t0004g0040a0001c0008t0004g0071 | 3 | HG02257.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2748-105C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 18/26 | chr12 | 15569312 | ||||||
| chr12:15569506
|
G | A | 3 | a0001c0002t0004g0056a0001c0002t0011g0082a0001c0002t0015g0095 | 3 | HG02109.hp1 HG03098.hp2 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.2829+8G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15569506 | ||||||
| chr12:15569621
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(62): Show | 65 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.2829+123A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15569621 | ||||||
| chr12:15569623
|
T | C | 1 | a0001c0002t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2829+125T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15569623 | ||||||
| chr12:15569741
|
C | T | 11 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2829+243C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15569741 | ||||||
| chr12:15569888
|
G | A | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0012g0084others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2829+390G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15569888 | ||||||
| chr12:15570193
|
T | C | 1 | a0001c0002t0004g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2829+695T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15570193 | ||||||
| chr12:15570210
|
G | A | 10 | a0001c0002t0002g0050a0001c0002t0002g0062a0001c0002t0002g0063others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2829+712G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15570210 | ||||||
| chr12:15570232
|
C | T | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2829+734C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15570232 | ||||||
| chr12:15570322
|
G | GT | 14 | a0001c0001t0001g0122a0001c0002t0002g0050a0001c0002t0002g0062others(11): Show | 14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2829+836dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 15570322 | |||||
| chr12:15570747
|
A | C | 1 | a0001c0003t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2829+1249A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15570747 | ||||||
| chr12:15570868
|
C | A | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2829+1370C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15570868 | ||||||
| chr12:15571083
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2829+1585G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571083 | ||||||
| chr12:15571220
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2829+1722G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571220 | ||||||
| chr12:15571262
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2829+1764A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571262 | ||||||
| chr12:15571281
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2829+1783C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571281 | ||||||
| chr12:15571294
|
T | A | 2 | a0001c0002t0008g0027a0001c0002t0008g0052 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2829+1796T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571294 | ||||||
| chr12:15571312
|
C | CAG | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2829+1815_2829+181 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 15571312 | |||||
| chr12:15571349
|
G | A | 7 | a0001c0001t0006g0068a0001c0001t0006g0094a0001c0001t0008g0011others(4): Show | 7 | HG00733.hp1 HG01261.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2829+1851G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571349 | ||||||
| chr12:15571431
|
T | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2829+1933T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571431 | ||||||
| chr12:15571450
|
G | T | 1 | a0001c0002t0008g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2829+1952G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571450 | ||||||
| chr12:15571458
|
T | C | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2829+1960T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571458 | ||||||
| chr12:15571727
|
G | A | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2829+2229G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571727 | ||||||
| chr12:15571847
|
TAA | T | 2 | a0001c0001t0002g0069a0001c0001t0002g0146 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2829+2351_2829+235 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 15571847 | |||||
| chr12:15571881
|
C | T | 1 | a0001c0004t0001g0024 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2829+2383C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15571881 | ||||||
| chr12:15572145
|
G | A | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2829+2647G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572145 | ||||||
| chr12:15572399
|
A | G | 2 | a0001c0002t0008g0027a0001c0002t0008g0052 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2829+2901A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572399 | ||||||
| chr12:15572556
|
C | T | 1 | a0001c0003t0001g0036 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2829+3058C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572556 | ||||||
| chr12:15572634
|
A | AT | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2829+3143dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 15572634 | |||||
| chr12:15572747
|
GTTTCTT | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(76): Show | 79 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.2829+3251_2829+325 others(10): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 15572747 | |||||
| chr12:15572757
|
GTATAA | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(76): Show | 79 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.2829+3260_2829+326 others(9): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572757 | ||||||
| chr12:15572764
|
A | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(76): Show | 79 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.2829+3266A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572764 | ||||||
| chr12:15572766
|
G | A | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(76): Show | 79 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.2829+3268G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572766 | ||||||
| chr12:15572896
|
A | G | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2829+3398A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572896 | ||||||
| chr12:15572908
|
C | T | 1 | a0001c0002t0003g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2829+3410C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572908 | ||||||
| chr12:15572945
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2829+3447C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572945 | ||||||
| chr12:15572995
|
G | A | 6 | a0001c0001t0003g0060a0001c0002t0002g0031a0001c0002t0003g0033others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.2829+3497G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15572995 | ||||||
| chr12:15573012
|
GGCTACAA others(4): Show |
G | 13 | a0001c0001t0002g0149a0001c0002t0002g0050a0001c0002t0002g0062others(10): Show | 13 | HG01109.hp1 HG02055.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.2829+3518_2829+352 others(15): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 15573012 | |||||
| chr12:15573021
|
C | G | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2829+3523C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573021 | ||||||
| chr12:15573453
|
A | C | 1 | a0001c0003t0001g0012 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2829+3955A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573453 | ||||||
| chr12:15573503
|
C | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 158 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(155): Show |
intron_variant | MODIFIER | c.2829+4005C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573503 | ||||||
| chr12:15573511
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2829+4013C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573511 | ||||||
| chr12:15573550
|
A | G | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2829+4052A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573550 | ||||||
| chr12:15573690
|
G | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 158 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(155): Show |
intron_variant | MODIFIER | c.2829+4192G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573690 | ||||||
| chr12:15573761
|
C | T | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2829+4263C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573761 | ||||||
| chr12:15573868
|
C | G | 1 | a0001c0003t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2829+4370C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573868 | ||||||
| chr12:15573963
|
A | G | 46 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(43): Show | 46 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2829+4465A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573963 | ||||||
| chr12:15573990
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(39): Show | 42 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.2829+4492C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15573990 | ||||||
| chr12:15574049
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(60): Show | 63 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.2829+4551A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574049 | ||||||
| chr12:15574108
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.2829+4610G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574108 | ||||||
| chr12:15574174
|
T | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2829+4676T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574174 | ||||||
| chr12:15574207
|
C | A | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2830-4646C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574207 | ||||||
| chr12:15574315
|
G | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0073others(1): Show | 4 | NA18943.hp2 NA18962.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2830-4538G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574315 | ||||||
| chr12:15574855
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(39): Show | 42 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.2830-3998C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574855 | ||||||
| chr12:15574944
|
A | G | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2830-3909A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574944 | ||||||
| chr12:15574990
|
T | G | 1 | a0001c0007t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2830-3863T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15574990 | ||||||
| chr12:15575072
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(38): Show | 41 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.2830-3781G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15575072 | ||||||
| chr12:15575116
|
G | A | 8 | a0001c0001t0003g0060a0001c0002t0002g0031a0001c0002t0003g0033others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.2830-3737G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15575116 | ||||||
| chr12:15575194
|
C | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(39): Show | 42 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.2830-3659C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15575194 | ||||||
| chr12:15575302
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(63): Show | 66 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2830-3551G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15575302 | ||||||
| chr12:15575311
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(68): Show | 71 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.2830-3542T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15575311 | ||||||
| chr12:15575764
|
C | T | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2830-3089C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15575764 | ||||||
| chr12:15576043
|
A | G | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2830-2810A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15576043 | ||||||
| chr12:15576426
|
A | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2830-2427A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15576426 | ||||||
| chr12:15576517
|
T | C | 5 | a0001c0001t0004g0115a0001c0002t0004g0056a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2830-2336T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15576517 | ||||||
| chr12:15576568
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2830-2285T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15576568 | ||||||
| chr12:15576905
|
T | C | 1 | a0001c0003t0001g0012 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2830-1948T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15576905 | ||||||
| chr12:15577140
|
C | A | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2830-1713C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577140 | ||||||
| chr12:15577390
|
C | G | 1 | a0001c0006t0004g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2830-1463C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577390 | ||||||
| chr12:15577392
|
T | C | 1 | a0002c0011t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2830-1461T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577392 | ||||||
| chr12:15577486
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2830-1367G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577486 | ||||||
| chr12:15577747
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2830-1106C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577747 | ||||||
| chr12:15577838
|
G | A | 15 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(12): Show | 15 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2830-1015G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577838 | ||||||
| chr12:15577855
|
GA | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2830-995delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr12 | 15577855 | |||||
| chr12:15577922
|
C | G | 1 | a0001c0001t0009g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2830-931C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577922 | ||||||
| chr12:15577928
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2830-925T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577928 | ||||||
| chr12:15577943
|
C | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2830-910C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15577943 | ||||||
| chr12:15578179
|
C | G | 1 | a0001c0002t0002g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2830-674C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578179 | ||||||
| chr12:15578207
|
A | T | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2830-646A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578207 | ||||||
| chr12:15578245
|
G | A | 1 | a0001c0001t0014g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2830-608G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578245 | ||||||
| chr12:15578599
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0130others(3): Show | 6 | HG01074.hp2 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2830-254T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578599 | ||||||
| chr12:15578605
|
T | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2830-248T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578605 | ||||||
| chr12:15578706
|
A | T | 1 | a0001c0003t0001g0150 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2830-147A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578706 | ||||||
| chr12:15578732
|
C | T | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2830-121C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578732 | ||||||
| chr12:15578790
|
T | TG | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.2830-63_2830-62ins others(1): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578790 | ||||||
| chr12:15578810
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(66): Show | 69 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.2830-43C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 19/26 | chr12 | 15578810 | ||||||
| chr12:15579136
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2920+193T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 20/26 | chr12 | 15579136 | ||||||
| chr12:15579331
|
A | T | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2920+388A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 20/26 | chr12 | 15579331 | ||||||
| chr12:15579389
|
A | G | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2920+446A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 20/26 | chr12 | 15579389 | ||||||
| chr12:15579841
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2921-198A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 20/26 | chr12 | 15579841 | ||||||
| chr12:15580021
|
T | C | 3 | a0001c0002t0001g0018a0001c0004t0001g0005a0001c0004t0001g0142 | 3 | HG01123.hp2 HG02300.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2921-18T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 20/26 | chr12 | 15580021 | ||||||
| chr12:15580182
|
T | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 33 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.2997+67T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 21/26 | chr12 | 15580182 | ||||||
| chr12:15580315
|
A | T | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2997+200A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 21/26 | chr12 | 15580315 | ||||||
| chr12:15580338
|
G | A | 3 | a0001c0001t0008g0011a0001c0002t0008g0027a0001c0002t0008g0052 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2997+223G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 21/26 | chr12 | 15580338 | ||||||
| chr12:15580342
|
A | G | 5 | a0001c0001t0004g0115a0001c0002t0004g0056a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2997+227A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 21/26 | chr12 | 15580342 | ||||||
| chr12:15580493
|
A | C | 3 | a0001c0002t0001g0018a0001c0004t0001g0005a0001c0004t0001g0142 | 3 | HG01123.hp2 HG02300.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2998-204A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 21/26 | chr12 | 15580493 | ||||||
| chr12:15580922
|
TA | T | 7 | a0001c0001t0003g0060a0001c0002t0003g0033a0001c0002t0003g0041others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.3132+95delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 15580922 | |||||
| chr12:15580964
|
G | A | 2 | a0001c0001t0007g0083a0001c0001t0007g0085 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3132+133G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | chr12 | 15580964 | ||||||
| chr12:15580978
|
A | C | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3132+147A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | chr12 | 15580978 | ||||||
| chr12:15580988
|
G | A | 2 | a0001c0009t0001g0153a0001c0009t0001g0154 | 2 | NA18946.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.3132+157G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | chr12 | 15580988 | ||||||
| chr12:15581298
|
C | CT | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(75): Show | 78 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.3133-361dupT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 15581298 | |||||
| chr12:15581298
|
CT | C | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0008g0011others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.3133-361delT | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 15581298 | |||||
| chr12:15581298
|
CTT | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.3133-362_3133-361d others(4): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 15581298 | |||||
| chr12:15581352
|
G | T | 12 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(9): Show | 12 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.3133-327G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | chr12 | 15581352 | ||||||
| chr12:15581543
|
G | GTTGTA | 53 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(50): Show | 53 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.3133-134_3133-133i others(7): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr12 | 15581543 | |||||
| chr12:15581649
|
T | C | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3133-30T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 22/26 | chr12 | 15581649 | ||||||
| chr12:15581865
|
C | T | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3255+64C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15581865 | ||||||
| chr12:15581866
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 33 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.3255+65G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15581866 | ||||||
| chr12:15581884
|
C | T | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3255+83C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15581884 | ||||||
| chr12:15582027
|
T | C | 7 | a0001c0001t0003g0060a0001c0002t0003g0033a0001c0002t0003g0041others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.3255+226T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582027 | ||||||
| chr12:15582121
|
C | A | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3255+320C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582121 | ||||||
| chr12:15582122
|
A | C | 12 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(9): Show | 12 | HG00423.hp2 HG00597.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3255+321A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582122 | ||||||
| chr12:15582209
|
G | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.3255+408G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582209 | ||||||
| chr12:15582324
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3255+523C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582324 | ||||||
| chr12:15582330
|
C | T | 1 | a0001c0003t0007g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3255+529C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582330 | ||||||
| chr12:15582462
|
A | G | 1 | a0003c0010t0013g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3255+661A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582462 | ||||||
| chr12:15582508
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 33 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.3255+707G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582508 | ||||||
| chr12:15582642
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 33 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.3255+841G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582642 | ||||||
| chr12:15582647
|
A | C | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3255+846A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582647 | ||||||
| chr12:15582686
|
C | T | 1 | a0001c0002t0007g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3255+885C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582686 | ||||||
| chr12:15582748
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(101): Show | 104 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.3255+947A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582748 | ||||||
| chr12:15582841
|
A | G | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3255+1040A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582841 | ||||||
| chr12:15582936
|
A | G | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3255+1135A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15582936 | ||||||
| chr12:15583049
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3255+1248C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583049 | ||||||
| chr12:15583075
|
C | G | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3255+1274C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583075 | ||||||
| chr12:15583160
|
T | C | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.3255+1359T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583160 | ||||||
| chr12:15583214
|
G | T | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3255+1413G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583214 | ||||||
| chr12:15583389
|
G | T | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3255+1588G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583389 | ||||||
| chr12:15583404
|
C | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.3255+1603C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583404 | ||||||
| chr12:15583479
|
C | CCA | 4 | a0001c0006t0004g0045a0001c0006t0004g0114a0001c0006t0004g0123others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.3255+1697_3255+169 others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr12 | 15583479 | |||||
| chr12:15583479
|
C | CCACA | 32 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(29): Show | 32 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.3255+1695_3255+169 others(8): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr12 | 15583479 | |||||
| chr12:15583496
|
C | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(71): Show | 74 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.3255+1695C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583496 | ||||||
| chr12:15583498
|
C | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(112): Show | 115 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.3255+1697C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583498 | ||||||
| chr12:15583500
|
A | C | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3255+1699A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583500 | ||||||
| chr12:15583768
|
G | T | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3255+1967G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15583768 | ||||||
| chr12:15584057
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 33 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.3255+2256T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584057 | ||||||
| chr12:15584076
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0138 | 3 | HG01934.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3255+2275G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584076 | ||||||
| chr12:15584176
|
G | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3255+2375G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584176 | ||||||
| chr12:15584230
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3255+2429A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584230 | ||||||
| chr12:15584424
|
T | C | 11 | a0001c0001t0003g0060a0001c0002t0003g0033a0001c0002t0003g0041others(8): Show | 11 | HG00423.hp2 HG00597.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.3256-2473T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584424 | ||||||
| chr12:15584481
|
T | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 33 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.3256-2416T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584481 | ||||||
| chr12:15584496
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3256-2401T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584496 | ||||||
| chr12:15584618
|
G | A | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3256-2279G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584618 | ||||||
| chr12:15584820
|
A | G | 5 | a0001c0001t0004g0115a0001c0002t0004g0056a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3256-2077A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584820 | ||||||
| chr12:15584874
|
C | A | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3256-2023C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15584874 | ||||||
| chr12:15585081
|
G | A | 5 | a0001c0002t0015g0095a0001c0005t0005g0096a0001c0005t0005g0097others(2): Show | 5 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3256-1816G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585081 | ||||||
| chr12:15585096
|
A | C | 3 | a0001c0002t0001g0018a0001c0004t0001g0005a0001c0004t0001g0142 | 3 | HG01123.hp2 HG02300.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.3256-1801A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585096 | ||||||
| chr12:15585102
|
A | G | 2 | a0001c0003t0001g0145a0001c0003t0001g0157 | 2 | HG01516.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3256-1795A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585102 | ||||||
| chr12:15585168
|
G | A | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3256-1729G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585168 | ||||||
| chr12:15585170
|
A | T | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3256-1727A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585170 | ||||||
| chr12:15585171
|
T | A | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3256-1726T>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585171 | ||||||
| chr12:15585230
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3256-1667G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585230 | ||||||
| chr12:15585592
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.3256-1305T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585592 | ||||||
| chr12:15585747
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.3256-1150A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585747 | ||||||
| chr12:15585778
|
C | T | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3256-1119C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585778 | ||||||
| chr12:15585779
|
T | C | 1 | a0001c0003t0017g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3256-1118T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585779 | ||||||
| chr12:15585801
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3256-1096G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585801 | ||||||
| chr12:15585802
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.3256-1095C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585802 | ||||||
| chr12:15585915
|
T | C | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3256-982T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15585915 | ||||||
| chr12:15585965
|
CACTT | C | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3256-928_3256-925d others(6): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr12 | 15585965 | |||||
| chr12:15586190
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3256-707A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15586190 | ||||||
| chr12:15586361
|
A | G | 1 | a0001c0002t0003g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3256-536A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15586361 | ||||||
| chr12:15586386
|
A | G | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3256-511A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15586386 | ||||||
| chr12:15586411
|
T | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.3256-486T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15586411 | ||||||
| chr12:15586428
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3256-469G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 23/26 | chr12 | 15586428 | ||||||
| chr12:15587176
|
A | T | 1 | a0001c0002t0003g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3410+125A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587176 | ||||||
| chr12:15587266
|
T | G | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3410+215T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587266 | ||||||
| chr12:15587299
|
T | C | 4 | a0001c0002t0006g0058a0001c0002t0006g0059a0001c0002t0006g0162others(1): Show | 4 | HG00733.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.3410+248T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587299 | ||||||
| chr12:15587333
|
A | G | 2 | a0001c0002t0003g0133a0001c0002t0003g0143 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3410+282A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587333 | ||||||
| chr12:15587357
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3410+306A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587357 | ||||||
| chr12:15587360
|
C | A | 32 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(29): Show | 32 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.3410+309C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587360 | ||||||
| chr12:15587544
|
A | G | 5 | a0001c0001t0004g0115a0001c0002t0004g0056a0001c0002t0011g0082others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3410+493A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587544 | ||||||
| chr12:15587856
|
A | G | 7 | a0001c0001t0003g0060a0001c0002t0003g0033a0001c0002t0003g0041others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.3410+805A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587856 | ||||||
| chr12:15587926
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.3410+875G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587926 | ||||||
| chr12:15587947
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 33 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.3410+896T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587947 | ||||||
| chr12:15587965
|
G | A | 4 | a0001c0002t0001g0077a0001c0004t0001g0099a0001c0004t0001g0100others(1): Show | 4 | HG01243.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3410+914G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587965 | ||||||
| chr12:15587994
|
A | T | 1 | a0001c0002t0003g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3410+943A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15587994 | ||||||
| chr12:15588327
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3411-1128C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15588327 | ||||||
| chr12:15588521
|
G | C | 11 | a0001c0001t0003g0060a0001c0002t0003g0033a0001c0002t0003g0041others(8): Show | 11 | HG00423.hp2 HG00597.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.3411-934G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15588521 | ||||||
| chr12:15588793
|
A | T | 4 | a0001c0005t0005g0096a0001c0005t0005g0097a0001c0005t0005g0098others(1): Show | 4 | HG00733.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3411-662A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15588793 | ||||||
| chr12:15589015
|
T | G | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3411-440T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15589015 | ||||||
| chr12:15589113
|
C | T | 2 | a0001c0002t0001g0141a0003c0010t0013g0054 | 2 | HG02683.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3411-342C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15589113 | ||||||
| chr12:15589300
|
C | T | 3 | a0001c0001t0008g0011a0001c0002t0008g0027a0001c0002t0008g0052 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3411-155C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | chr12 | 15589300 | ||||||
| chr12:15589379
|
GA | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.3411-63delA | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr12 | 15589379 | |||||
| chr12:15589379
|
GAA | G | 16 | a0001c0001t0003g0060a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 16 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.3411-64_3411-63del others(2): Show |
PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr12 | 15589379 | |||||
| chr12:15589632
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3546+42C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15589632 | ||||||
| chr12:15589654
|
A | G | 2 | a0001c0002t0002g0050a0001c0005t0002g0109 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3546+64A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15589654 | ||||||
| chr12:15590510
|
T | C | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3546+920T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15590510 | ||||||
| chr12:15590521
|
G | T | 15 | a0001c0001t0003g0060a0001c0001t0005g0102a0001c0001t0005g0103others(12): Show | 15 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.3546+931G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15590521 | ||||||
| chr12:15590808
|
T | C | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3546+1218T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15590808 | ||||||
| chr12:15590902
|
A | G | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3546+1312A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15590902 | ||||||
| chr12:15591069
|
C | A | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.3546+1479C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15591069 | ||||||
| chr12:15591378
|
A | C | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3546+1788A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15591378 | ||||||
| chr12:15591379
|
C | A | 16 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3546+1789C>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15591379 | ||||||
| chr12:15591582
|
T | C | 1 | a0001c0005t0005g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3546+1992T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15591582 | ||||||
| chr12:15591634
|
G | T | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.3546+2044G>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15591634 | ||||||
| chr12:15591644
|
C | G | 7 | a0001c0001t0003g0060a0001c0002t0003g0033a0001c0002t0003g0041others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.3546+2054C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15591644 | ||||||
| chr12:15591882
|
T | G | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3546+2292T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15591882 | ||||||
| chr12:15592021
|
C | T | 1 | a0001c0003t0001g0036 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3546+2431C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15592021 | ||||||
| chr12:15592278
|
G | C | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.3547-2659G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15592278 | ||||||
| chr12:15592320
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.3547-2617G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15592320 | ||||||
| chr12:15592453
|
C | T | 17 | a0001c0001t0002g0069a0001c0001t0002g0146a0001c0001t0002g0149others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.3547-2484C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15592453 | ||||||
| chr12:15592606
|
A | G | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3547-2331A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15592606 | ||||||
| chr12:15592865
|
A | C | 1 | a0001c0006t0004g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3547-2072A>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15592865 | ||||||
| chr12:15593109
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.3547-1828G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15593109 | ||||||
| chr12:15593195
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3547-1742T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15593195 | ||||||
| chr12:15593291
|
A | G | 8 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0002t0005g0075others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3547-1646A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15593291 | ||||||
| chr12:15593373
|
T | C | 1 | a0001c0002t0002g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3547-1564T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15593373 | ||||||
| chr12:15593765
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3547-1172C>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15593765 | ||||||
| chr12:15593905
|
T | G | 9 | a0001c0001t0006g0068a0001c0001t0006g0094a0001c0001t0008g0011others(6): Show | 9 | HG00733.hp1 HG01261.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3547-1032T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15593905 | ||||||
| chr12:15594130
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.3547-807T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15594130 | ||||||
| chr12:15594158
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3547-779T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15594158 | ||||||
| chr12:15594165
|
T | C | 1 | a0001c0002t0016g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3547-772T>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15594165 | ||||||
| chr12:15594557
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3547-380A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15594557 | ||||||
| chr12:15594805
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3547-132A>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15594805 | ||||||
| chr12:15594918
|
T | G | 1 | a0001c0004t0001g0017 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3547-19T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 25/26 | chr12 | 15594918 | ||||||
| chr12:15595086
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.*16+29C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 26/26 | chr12 | 15595086 | ||||||
| chr12:15595172
|
G | A | 1 | a0001c0002t0001g0008 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*16+115G>A | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 26/26 | chr12 | 15595172 | ||||||
| chr12:15595560
|
C | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.*16+503C>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 26/26 | chr12 | 15595560 | ||||||
| chr12:15595649
|
A | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.*17-441A>T | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 26/26 | chr12 | 15595649 | ||||||
| chr12:15595757
|
T | G | 7 | a0001c0001t0003g0060a0001c0002t0003g0033a0001c0002t0003g0041others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.*17-333T>G | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 26/26 | chr12 | 15595757 | ||||||
| chr12:15595901
|
G | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.*17-189G>C | PTPRO | ENSG00000151490.15 | transcript | ENST00000281171.9 | protein_coding | 26/26 | chr12 | 15595901 |